HUMAN UMBILICAL CORD BLOOD-DERIVED MONOCYTES FOR TREATMENT OF NEURODEGENERATIVE DISEASES AND DISORDERS

Abstract

Human umbilical cord blood-derived monocytes that markedly promote A clearance through heterodimerization of sAPP with A and resultant sAPP production for prevention or treatment of Alzheimer's disease and other neurodegenerative disorders (including stroke and TBI). It was discovered that multiple low-dose infusions of human umbilical cord blood cells (HUCBCs) ameliorate cognitive impairments and reduce A-associated neuropathology in PSAPP transgenic mice, which markedly promotes amyloid precursor protein (APP) -cleavage and resultant sAPP production for pharmaceutical purposes, in particular for treating or slowing the progression of Alzheimer's disease.

Claims

1. A method of preventing or treating a neurodegenerative disease or disorder, comprising administering a therapeutically effective amount of human umbilical cord blood-derived monocytes.

2. A method as in claim 1, wherein the neurodegenerative disease or disorder is selected from the group consisting of Alzheimer's disease, stroke, and traumatic brain injury.

3. A method as in claim 1, wherein the human umbilical cord blood-derived monocytes are pretreated with exogenous soluble amyloid precursor protein alpha (sAPP).

4. A method as in claim 2, wherein the human umbilical cord blood-derived monocytes are administered in multiple low-dose infusions.

5. A composition comprising sAPP-treated aged monocytes formed by heterodimerization of sAPP with amyloid beta (A).

6. A method of preventing or treating a neurodegenerative disease or disorder, comprising administering a therapeutically effective amount of sAPP-treated aged monocytes formed by heterodimerization of sAPP with A.

7. A method as in claim 6, wherein the neurodegenerative disease or disorder is selected from the group consisting of Alzheimer's disease, stroke, and traumatic brain injury.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] For a fuller understanding of the invention, reference should be made to the following detailed description, taken in connection with the accompanying drawings, in which:

[0023] FIG. 1A depicts FACS analysis of surface expression markers in human umbilical cord blood monocytes, such as CD14.sup.+, total surface APP, and full-length APP, using anti-CD14.sup.+ antibodies by flow cytometry from HUCBC and HUCBC-derived monocytes.

[0024] FIG. 1B depicts FACS analysis of surface expression markers in human umbilical cord blood monocytes, such as CD14.sup.+, total surface APP, and full-length APP, using anti-A-N-terminal (6E10) antibodies by flow cytometry from HUCBC and HUCBC-derived monocytes.

[0025] FIG. 1C depicts FACS analysis of surface expression markers in human umbilical cord blood monocytes, such as CD14.sup.+, total surface APP, and full-length APP, using anti-APP-C-terminal (pAb751/770) antibodies by flow cytometry from HUCBC and HUCBC-derived monocytes.

[0026] FIG. 1D depicts cell lysates obtained from HUCBC and HUCBC-derived monocytes subjected to WB analysis. The percentage of CD14, 6E10, and pAb751/770 APP positive cells in each quadrant is indicated. Overall, the purity of HUCBC-derived monocytes was found to be almost 95%.

[0027] FIG. 2A is a schematic illustration of HUCBC treatment schedule and testing for cognitive and motor function in PSAPP and WT mice. Both PSAPP and age-matched WT control mice were tested after short term systemic administration of monocytes.

[0028] FIG. 2B shows that the cognitive function was presented as numbers of entry-arm errors before finding the platform. WCB- and CB-M-treated PSAPP mice showed better behavioral performance than PBS treated group. In addition, CB-M-treated PSAPP mice showed improve behavioral performance than WCB-treated group. In contrast, MD-CB-treated group showed no cognitive improvement. WT littermates also showed similar tendency at each treatment condition. All data are presented as meanSEM (*P<0.05; **P<0.01), and analyzed by one-way analysis of variance (ANOVA) with LSD post-hoc test.

[0029] FIG. 2C shows that motor function was also assessed using rotarod test after treatment. WCB-treated PSAPP mice showed enhance motor activity, reflected as enhanced latency to fall, but not statistically significant compared to PBS-treated group. CB-M-treated PSAPP mice showed significantly improved motor activity compared to MD-CB-treated mice on day 1. Similarly, CB-M-treated WT control mice showed significant improvement in motor activity compared to MD-CB-treated group on both days 1 and 2. All data are presented as meanSEM (*P<0.05; **P<0.01), and analyzed by one-way analysis of variance (ANOVA) with one-way ANOVA with Bonferroni post-hoc test. Overall, FIGS. 2A-2C show that short term (two-month) administration of HUCBC-derived monocytes improves learning, memory and motor function.

[0030] FIG. 3A is a schematic diagram of HUCBC treatment schedule and behavioral testing in PSAPP and WT mice. Both PSAPP and aged-match WT control mice were cognitively tested after long term monocytes administration.

[0031] FIG. 3B shows that hippocampal-dependent learning and memory function was assessed by RAWM test after treatment completion. The cognitive activity was presented as numbers of entry-arm errors before finding the platform. Consistent with the two-month treatment data, WCB- and CB-M-treated PSAPP mice showed improved cognitive function compared with PBS-treated PSAPP mice. WT littermates also showed similar effects with each treatment paradigm. MD-CB-treatment did not show behavioral improvement, and even exacerbated the cognitive function of WT mice. All data are shown as the meanSEM (*P<0.05; **P<0.01) and analyzed by one-way analysis of variance (ANOVA) with LSD post-hoc test.

[0032] FIG. 3C shows that motor activity was assessed using rotarod test after monocytes administration. WCB- or CB-M-treated PSAPP mice significantly improve the motor activity, assessed as latency to fall, compared to PBS-treated group, while MD-CB treatment progressively impaired the motor function of WT control group. All data are shown as the meanSEM (*P<0.05; **P<0.01) and analyzed by one-way analysis of variance (ANOVA) with one-way ANOVA with Bonferroni post-hoc test. Overall, FIGS. 3A-3C show that long term (four-month) administration of HUCBC-derived monocyte improves learning, memory and motor function.

[0033] FIG. 4A shows that HUCBC (WCB) and HUCBC-derived monocytes (CB-M) significantly reduce -amyloid plaques in retrosplenial cortex (RSC), entorhinal cortex (EC), and hippocampus (H) of PSAPP mice, as determined by immunohistochemical staining with anti-A.sub.17-24 antibody (4G8).

[0034] FIG. 4B shows that the percentage quantification of immunoreactive areas in area of interest (H region) by image analysis for each treatment group using 4G8 antibody (n=4).

[0035] FIG. 4C shows that detergent-soluble A.sub.1-40 and A.sub.1-42 levels in brain homogenates of PSAPP mice were analyzed by A ELISA. Data are represented as meanSD of A.sub.1-40,42 (ng/mg of total protein). A t-test for independent samples reveals significant differences between HUCBC or HUCBC-derived monocyte (CB-M) treatment and PBS control groups (**P<0.01), but no significant difference between whole HUCBC (WCB) and CB-M treatment groups (P>0.05). Overall, FIGS. 4A-4C show that HUCBC-derived monocytes reduce A pathology.

[0036] FIG. 5A depicts a quantitative measurement of A.sub.1-42 internalization by cord and aged blood monocytes. Extracellular (upper panel) and cell-associated (lower panel) FITC-A.sub.1-42 was measured from supernatants and lysates respectively using fluorimeter. HUCBC-derived monocytes (CB-M) shows lower level of extracellular A.sub.1-42 (top left panel) and as expected higher level of cell-associated A.sub.1-42 than aged BC-M (bottom left panel). Internalization of A.sub.1-42 by aged human blood cell-derived monocytes (BC-M) was enhanced by sAPP treatment (100 ng/ml). Monocyte scavenger receptor class A (SR-A) appears to be the cell surface receptor that account for the internalization A.sub.1-42 SR-A ligand decreased A.sub.1-42 internalization during sAPP treatment. Data are represented as relative mean fluorescence (meanSD) for each sample at 37 C. divided by mean fluorescence at 4 C. (n=4 for each condition) (*P<0.05, **P<0.01, *** P<0.001).

[0037] FIG. 5B depicts in vitro confocal images of A phagocytosis by cord and aged blood derived monocytes. Monocytes were obtained, characterized by flow cytometry, incubated with purified FITC-A.sub.1-42 peptide (1 M) for 60 minutes, and then assessed by confocal microscopy. Primary monocytes were treated, fixed and imaged using confocal microscopy equipped with Normarski optics. Blue fluorescence represents monocytes and green fluorescence represents FITC-labeled A.sub.1-42. Merged image shows significant internalization of A.sub.1-42 within the cytoplasm of CB-M as shown by most of the green fluorescence localized in the cytoplasmic compartment (left upper panel) while aged BC-M shows significant reduction of A.sub.1-42 internalization (left lower panel). Aged BC-M treated with sAPP shows significantly increased A.sub.1-42 internalization in the cytoplasm (right upper panel), while SR-A ligand decreased A.sub.1-42 internalization inside the cytoplasm during sAPP treatment (right middle panel). Unlabeled (naked) A.sub.1-42 competitively reduced internalization of FITC-A.sub.42 by CB-M (left middle panel).

[0038] FIG. 6A shows conditioned media of CHO-APPwt and CHO-APPswe cells expressing APP, As and sAPP immunoprecipitated with anti-A.sub.17-27 antibody (4G8), followed by WB detection with anti-A.sub.1-16 monoclonal antibody (6E10) (left panel) or an anti-APP N-terminal antibody (22C11) (right panel). WB with 6E10 shows both sAPP and A bands (left panel), but WB with 22C11 only shows sAPP band (right panel).

[0039] FIG. 6B depicts further confirmation of heterodimerization by immunoprecipitating with anti-APP N-terminal antibody (22C11) and WB detection with 6E10, revealing both sAPP and A bands. Overall, FIGS. 6A-6B prove sAPP and A heterodimerization at monocyte's cell surface via immunoprecipitation of sAPP and As in cell culture.

[0040] FIG. 7A is a diagram showing the sequence of truncated sAPP (top) and A.sub.42 (bottom). Note that Ahx (aminohexanoic acid), a common hydrophobic spacer.

[0041] FIG. 7B depicts analysis by WB with anti-A.sub.1-16 antibody (82E1) after truncated sAPP was incubated with synthesized A.sub.1-42 and immunoprecipitated with anti-A.sub.17-27 antibody (4G8). For negative control, conditioned media from CHO/APPswe cells underwent the same treatment in this experiment. 82E1 picked up both A.sub.1-42 (4 kDa, upper band) and truncated sAPP (4 kDa, lower band) after incubating truncated sAPP with synthesized A.sub.42 (lanes 1 and 2) but only A.sub.1-42 band showed up in control (lane 3).

[0042] FIG. 7C depicts analysis by WB with an anti-APP N-terminal monoclonal antibody (22C11) after truncated sAPP was incubated with synthesized A.sub.1-42 and immunoprecipitated with anti-A.sub.17-27 antibody (4G8). 22C11 only picked up truncated sAPP (4 kDa) (lanes 1 and 2) after truncated sAPP was incubated with synthesized A.sub.42 and as expected only sAPP (100 kDa) (lane 3) in CHO/APPswe conditioned media. Overall, FIGS. 7A-7C prove that APP.sub.672-687 (A.sub.1-16) region is responsible for sAPP/A heterodimerization.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

[0043] In the following detailed description of the preferred embodiments, reference is made to the accompanying drawings, which form a part thereof, and within which are shown by way of illustration specific embodiments by which the invention may be practiced. It is to be understood that other embodiments may be utilized and structural changes may be made without departing from the scope of the invention.

[0044] As used in this specification and the appended claims, the singular forms a, an, and the include plural referents unless the content clearly dictates otherwise. As used in this specification and the appended claims, the term or is generally employed in its sense including and/or unless the context clearly dictates otherwise.

[0045] As used herein, about means approximately or nearly and in the context of a numerical value or range set forth means 15% of the numerical. In an embodiment, the term about can include traditional rounding according to significant figures of the numerical value. In addition, the phrase about x to y includes about x to about y.

[0046] As used herein, treat, treatment, treating, and the like refer to acting upon a condition (e.g., neurodegenerative disease/disorder or symptom thereof) with an agent (e.g., HUCBC-derived monocytes, sAPP-treated aged monocytes) to affect the condition by improving or altering it. The improvement or alteration may include an improvement in symptoms or an alteration in the physiologic pathways associated with the condition. The aforementioned terms cover one or more treatments of a condition in a patient (e.g., a mammal, typically a human or non-human animal of veterinary interest), and includes: (a) reducing the risk of occurrence of the condition in a subject determined to be predisposed to the condition but not yet diagnosed, (b) impeding the development of the condition, and/or (c) relieving the condition, e.g., causing regression of the condition and/or relieving one or more condition symptoms.

[0047] As used herein, the terms prophylactically treat or prophylactically treating refers completely or partially preventing (e.g., about 50% or more, about 60% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, or about 99% or more) a condition or symptom thereof and/or may be therapeutic in terms of a partial or complete cure or alleviation for a condition and/or adverse effect attributable to the condition.

[0048] A pharmaceutically acceptable excipient, pharmaceutically acceptable diluent, pharmaceutically acceptable carrier, or pharmaceutically acceptable adjuvant means an excipient, diluent, carrier, and/or adjuvant that are useful in preparing a pharmaceutical composition that are generally safe, non-toxic and neither biologically nor otherwise undesirable, and include an excipient, diluent, carrier, and adjuvant that are acceptable for veterinary use and/or human pharmaceutical use. A pharmaceutically acceptable excipient, diluent, carrier and/or adjuvant as used in the specification and claims includes one or more such excipients, diluents, carriers, and adjuvants.

[0049] The term therapeutically effective amount as used herein describes concentrations or amounts of components such as agents which are effective for producing an intended result. Compositions according to the present invention may be used to effect a favorable change in the neurodegenerative disease/disorder or symptom thereof, whether that change is an improvement, relieving to some extent one or more of the symptoms of the condition being treated, and/or that amount that will prevent, to some extent, one or more of the symptoms of the condition that the host being treated has or is at risk of developing, or a complete cure of the disease or condition treated.

[0050] The term administration or administering is used throughout the specification to describe the process by which a composition comprising HUCBC-derived monocytes or sAPP-treated aged monocytes as active agent, are delivered to a patient or individual for therapeutic purposes. The composition of the subject invention and methodology in use thereof can be administered a number of ways including, but not limited to, parenteral (such term referring to intravenous and intra-arterial as well as other appropriate parenteral routes), subcutaneous, peritoneal, inhalation, vaginal, rectal, nasal, or instillation into body compartments.

[0051] Administration will often depend upon the amount of compound administered, the number of doses, and duration of treatment. In an embodiment, multiple doses of the agent are administered. The frequency of administration of the agent can vary depending on any of a variety of factors, such as stage of the neurodegenerative disease/disorder, and the like. The duration of administration of the agent, e.g., the period of time over which the agent is administered, can vary, depending on any of a variety of factors, including patient response, etc.

[0052] The amount of the agent contacted (e.g., administered) can vary according to factors such as the degree of susceptibility of the individual, the age, sex, and weight of the individual, idiosyncratic responses of the individual, the dosimetry, and the like. Detectably effective amounts of the agent of the present disclosure can also vary according to instrument and film-related factors. Optimization of such factors is well within the level of skill in the art, unless otherwise noted.

[0053] As used herein, the term subject, patient, or organism includes humans and mammals (e.g., mice, rats, pigs, cats, dogs, and horses). Typical hosts to which an agent(s) of the present disclosure may be administered will be mammals, particularly primates, especially humans. For veterinary applications, a wide variety of subjects will be suitable, e.g., livestock such as cattle, sheep, goats, cows, swine, and the like; poultry such as chickens, ducks, geese, turkeys, and the like; and domesticated animals particularly pets such as dogs and cats. For diagnostic or research applications, a wide variety of mammals will be suitable subjects, including rodents (e.g., mice, rats, hamsters), rabbits, primates, and swine such as inbred pigs and the like.

[0054] It should be noted that ratios, concentrations, amounts, and other numerical data may be expressed herein in a range format. It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a concentration range of about 0.1% to about 5% should be interpreted to include not only the explicitly recited concentration of about 0.1 wt % to about 5 wt %, but also include individual concentrations (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.2%, 3.3%, and 4.4%) within the indicated range.

[0055] Discussed herein are human umbilical cord blood-derived monocytes that markedly promote A clearance through heterodimerization of sAPP with A and resultant sAPP production for prevention or treatment of Alzheimer's disease and other neurodegenerative disorders (including stroke and TBI). It was discovered that multiple low-dose infusions of human umbilical cord blood cells (HUCBCs) ameliorate cognitive impairments and reduce A-associated neuropathology in PSAPP transgenic mice, which markedly promotes amyloid precursor protein (APP) -cleavage and resultant sAPP production for pharmaceutical purposes, in particular for treating or slowing the progression of Alzheimer's disease.

[0056] Study

[0057] The current inventors have reported that human umbilical cord blood cells (HUCBCs) modulated inflammation, diminished A pathology, and reduced behavioral deficits in PSAPP transgenic mice (9). Based on the prior art and the current inventors' previous study (9,36), the present study sought to modify the current inventors' previous HUCBCs study in such a way that only the CD14.sup.+ monocyte fraction (HUCBC-derived monocytes), isolated from total HUCBCs, would be infused peripherally over short and long term periods of time in PSAPP and WT mice.

[0058] The present study attempts to determine which mononuclear cell (MNC) population was conferring these effects. Accumulated AD research has suggested that monocytes among MNCs are contributory to promoting A clearance (9,31,32,20). Therefore, it was examined whether monocytes purified from HUCBCs would have beneficial outcomes on the reduction of AD-like pathology and rescue of cognitive impairments in PSAPP transgenic AD mice. PSAPP mice and their wild-type littermates were treated monthly with a peripheral HUCBC-derived monocyte infusion over a period of 2 and 4 months, followed by behavioral evaluations as well as biochemical and histological analyses. The present study extends on the HUCBCs AD therapy to: (1) examine whether monocytes are responsible for the beneficial effects against AD observed in HUCBCs therapeutics, and (2) determine the mechanism by which these salutary effects occur.

[0059] The current inventors discovered that multiple low-dose infusions of human umbilical cord blood cells (HUCBCs) ameliorate cognitive impairments and reduce A-associated neuropathology in PSAPP transgenic mice. In the present study, it was examined whether monocytes, as important components of HUCBCs, would have beneficial outcomes on the reduction of AD-like pathology and associated cognitive impairments in PSAPP transgenic AD model mice. PSAPP mice and their wild-type littermates were treated monthly with an infusion of peripheral human umbilical cord blood cell (HUCBC-derived monocytes over a period of 2 and 4 months, followed by behavioral evaluations, biochemical, and histological analyses. The principal findings of the present study confirmed that monocytes derived from HUCBCs (CB-M) play a central role in HUCBC-mediated cognition-enhancing and A-pathology ameliorating activities.

[0060] Importantly, it was found that compared with CB-M, aged monocytes showed an ineffective phagocytosis of A, while exogenous soluble amyloid precursor protein alpha (sAPP) could reverse this deficiency. Pretreating monocytes with sAPP upregulates A internalization. Further studies suggested that sAPP could form a heterodimer with As, with the APP672-688 (A1-16) region being responsible for this effect. This in turn promoted binding of these heterodimers to monocyte scavenger receptors and thus promoted enhanced A clearance. In summary, the current study suggests that peripheral monocytes contribute to A clearance through heterodimerization of sAPP with A. Further, declined or impaired sAPP production, or reduced heterodimerization with A, would cause a deficiency in A clearance and thus accelerate the pathogenesis of AD.

A. MATERIALS AND METHODS

[0061] All experiments were performed in accordance with the guidelines of the National Institutes of Health, and all animal studies were approved by the University of South Florida (USF) Institutional Animal Care and Use Committee. Animals were humanely cared for during all experiments, and all efforts were made to minimize animal suffering. Animals were anesthetized with isoflurane (50 mg/kg) and euthanized by transcardial perfusion with ice-cold physiological saline containing heparin (10 units/mL). In this study, use of human cord blood cells was involved. Ninety-five to 98% mononuclear cells from HUCBCs were provided by SANERON CCEL Therapeutics Inc. (Tampa, Fla.). SANERON used de-identified HUCBCs donations from certified commercial sources.

[0062] i. Animals

[0063] PSAPP (APPswe/PS1DE9) mice and their wild-type (WT) littermates were obtained from the Jackson Laboratory (Bar Harbor, Me.). PSAPP mice overproduce human A.sub.1-40 and A.sub.1-42 peptides (APP Swedish mutation with a PS1 deletion in exon 9) and from about 4 months develop progressive cerebral A deposits with learning and memory impairment, albeit without neuronal loss (9,5,17,1,23). All mice were characterized by PCR genotyping for mutant human APP and presenilin 1 (PS1) transgenes. Thus, all mice used in this study are genetically comparable. Both PSAPP mice and their WT littermates were maintained on a 12 hour-light/12 hour-dark cycle at ambient temperature and humidity. All cohorts were housed in the animal facility at the USF, Morsani College of Medicine (Johnnie B. Byrd Sr. Alzheimer's Center and Research Institute, Tampa, Fla.). Animals were fed standard rodent chow and water ad libitum. For the cord blood-derived monocyte experiments, 5.5-month old PSAPP mice and WT littermates were used. All cohorts were female and this served to eliminate the possibility of gender discrepancies among groups. All animals in these experiments were observed in a blinded, randomized approach.

[0064] ii. HUCBCs Preparation

[0065] HUCBCs, comprised of 95-98% mononuclear cells, were obtained using a proprietary density gradient solution (DSS-001) developed by SANERON and GE HEALTHCARE. Our purified HUCBCs were cryopreserved and stored in liquid nitrogen at 210 C. HUCBCs were thawed prior to transplantation, at 37 C. for 4 minutes, washed in 0.05 M phosphate-buffered saline (PBS), assessed for cell quantification and viability (CELLDYN, VI-CELL, Indianapolis Ind.), and suspended in PBS to achieve a cell concentration of 210.sup.5 cells per 100 L for each infusion.

[0066] iii. HUCBC-Derived Monocyte Acquisition

[0067] The HUCBCs suspension was centrifuged and re-suspended in monocyte buffer, containing 0.5% bovine serum albumin (BSA), and 2 mM EDTA in PBS. Monocytes were separated via positive selection using the MACS Miltenyi biotec CD14.sup.+ MicroBeads human kit (MILTENYI BIOTEC Inc., San Diego, Calif.) (44). CD14.sup.+ MicroBeads were added to the cell suspension and incubated for 15 minutes at 4 C. Cells were washed, re-suspended in PBS and run through a column in a magnetic separator. Cells were allowed to flow into a collection flask and this comprised the monocyte-deficient cord blood (MD-CB) infused in the cohorts. The column was removed and flushed with buffer to obtain an enriched population of cord blood derived monocytes (CB-M). Acquired monocyte populations were characterized using flow cytometry. Cell counts and viability were then carried out as described. Cells were centrifuged, re-suspended in PBS twice and aliquots of 210.sup.5 cells per 100 L concentration per mouse were made.

[0068] iv. Flow Cytometry Analysis of HUCBC-Derived Monocytes

[0069] HUCBC-derived monocytes were stained for identification of the subset monocyte population expressing CD14.sup.+ using an anti-CD14.sup.+ monoclonal antibody (SIGMA-ALDRICH, St. Louis, Mo.), and FACS analysis by ACCURI C6 Flow Cytometer (Rochester, Minn.). Only monocyte populations composed of 93% CD14.sup.+ cells were used in the study. In addition, further flow cytometry analysis of HUCBC-derived monocytes for membrane surface associated APP and full-length APP was conducted using an anti-A N-terminal monoclonal antibody (6E10, 1:2,000; COVANCE RESEARCH PRODUCTS, Emeryville, Calif.) and an anti-APP C-terminal polyclonal antibody (pAb751/770, 1:1,000; CALBIOCHEM, Billerica, Mass.) according to manufacturer specifications.

[0070] v. Western Blot Analysis for APP Levels

[0071] Cell lysates from cultured HUCBCs and HUCBC-monocytes were assayed by Western blot (WB) analysis. In brief, cells were cultured then lysed in ice-cold lysis buffer (1 mM Na.sub.3VO.sub.4, 150 mM NaCl, 1 mM EDTA, 2.5 mM sodium pyrophosphate, 20 mM Tris pH 7.5, 1 mM EGTA, 1% v/v Triton X-100, 1 mM PMSF, 1 mM -glycerolphosphate, 1 g/mL leupeptin). Inherent proteins were separated using 10% gel, transferred to 0.2-m nitrocellulose membranes (BIO-RAD, Hercules, Calif.) and visualized using standard immunoblotting protocol. All antibodies were diluted in 0.05 M Tris-buffered saline (TBS) containing 5% (w/v) nonfat dry milk. Membranes were immunoblotted with appropriate primary antibody and then probed using an anti-mouse IgG (1:2,000; CELL SIGNALING TECHNOLOGY, Danvers, Mass.) or an anti-rabbit IgG (1:10,000; THERMO FISHER SCIENTIFIC, Waltham, Mass.) secondary antibody conjugated with horseradish peroxidase. Proteins were detected with Super Signal West Femto Maximum Sensitivity Substrate (THERMO FISHER SCIENTIFIC, Waltham, Mass.) and BIOMAX-MR Film (THERMO FISHER SCIENTIFIC, Waltham, Mass.). Primary antibodies include an anti-APP N-terminal monoclonal antibody (22C11, 1:2,000, EMD Millipore, Temecula, Calif.), an anti-APP C-terminal polyclonal antibody (pAb751/770, 1:1,000) to evaluate APP expression, an anti-A.sub.1-16 monoclonal antibody (6E10, 1:2,000), and an anti--actin monoclonal antibody (1:4,000; SIGMA-ALDRICH).

[0072] vi. HUCBC-Derived Monocyte Infusion

[0073] Briefly, 23 PSAPP mice and WT littermates were randomly assigned into the following four treatment groups: whole HUCBCs (WCB, n=6), HUCBC-derived monocytes (CB-M, n=6), monocyte-deficient HUCBC (MD-CB, n=6), or PBS (n=5). With respect to the number of PSAPP and WT mice used in the study, each group, with the exception of the PBS treated cohorts, comprised n=3 animals per strain. The PBS treated group contained WT (n=2) and PSAPP (n=3). The right tail vein of PSAPP mice or their WT littermates was identified and vasodilated using warm water and then 210.sup.5 cells/100 L WCB, CB-M, MD-CB or 100 L PBS per mouse was delivered via right tail vein injection. The injection was performed four times over two months and six times over four months. HUCBCs were infused at the end of weeks 1, 3, 5 and 7 for the 2-month treatment and at the end of weeks 1, 3, 5, 7, 9, 11, 13 and 15 for the 6-month treatment. These agents were administered intravenously since it is a readily available approach and shown previously by the current inventors to be effective in reducing AD pathology in mice (9). However, other suitable methods of administration are contemplated herein as well.

[0074] vii. Behavioral Tests

[0075] Motor and cognitive evaluations were conducted at the end of the 2-month treatment (7.5 months of age) or at the end of the 4-month treatment (9.5 months of age) using the rotarod test for motor activity, as well as the radial arm water maze (RAWM) test and the visible platform in an open pool test for cognitive ability.

[0076] Rotarod test. For two consecutive days, mice underwent rotarod test. Mice were positioned on the rod (diameter 3.6 cm) of the equipment (ROTAROD 7650 accelerating model UGO BASILE, Biological Research Apparatus, Varese, Italy). The rod was set at 4.0 rpm and mice were placed 5 at a time on the rod. Trial time was five minutes and the rod steadily accelerated from 4.0 rpm up to 40.0 rpm. Mice were evaluated by the time they were able to retain their balance position on the rod.

[0077] Radial arm water maze test. All mice received 2 days of 15 swims or trials per day. Each swim culminated either when a visible or a submerged underwater goal was located or after 1 minute had elapsed. Briefly the mouse was dropped into a random start arm (predetermined on a score sheet) and allowed to swim until it located and climbed onto the platform (goal) over a period of 1 minute. Errors were recorded as any entry into an incorrect arm or failure to enter any arm for the initial 15 seconds of the trial. Results were analyzed as number of errors made.

[0078] Visible platform in an open pool swim test. For verification of whether the animals possessed the skills sufficient to complete the water maze task, the visible platform was used in an open pool swim test. In brief, it was performed in the same pool as the radial arm water maze test; however, the triangular wedges were removed and the pool was left open with a visible platform in an imagined quadrant. Latency to find and ascend the platform was measured (60 seconds maximum).

[0079] viii. Tissue Preparation

[0080] Subsequent to neurocognitive evaluations, cohorts were anesthetized with isoflurane and euthanized at either 7.5 or 9.5 months of age. Hind limbs (for bone marrow) and 500 peripheral blood were initially collected and the mice were then perfused transcardially with an ice-cold physiological saline. Brains were rapidly isolated and the left hemispheres were frozen immediately in liquid nitrogen and stored at 80 C. For molecular analysis, the left hemispheres were sonicated in RIPA buffer (Cell Signaling Technology) and centrifuged at 14,000 rpm for 1 hour at 4 C. Supernatant was transferred to a new tube for soluble A analysis and the pellet was used for insoluble A extraction as described previously (42). The right hemispheres were placed in 4% paraformaldehyde in PBS at 4 C. overnight, and then transferred to a graded series of sucrose solutions (10%, 20%, and 30%, each at 4 C. overnight) for cryostat sectioning. Sequential 25-m coronal sections were cut and free-floating sections were then stored at 4 C. in 24-well plates containing PBS with 100 mM sodium azide.

[0081] ix. Immunohistochemical Analysis

[0082] Sections were immunohistochemically stained using an anti-A.sub.17-26 monoclonal antibody (4G8, 1:200; COVANCE RESEARCH PRODUCTS) in conjunction with the VECTASTAIN ABC Elite kit (VECTOR LABORATORIES, Burlingame, Calif.) coupled with diaminobenzidine substrate. For all the staining, a set of sections without adding primary antibody was used as negative staining control. A burden (A immunoreactive area) was determined by quantitative image analysis of A plaques burden in the retrosplenial cortex (RSC), entorhinal cortex (EC), and hippocampus (H) brain regions of PSAPP mice and their WT littermates for each of the groups treated. Images of five 25-m sections (150-m apart) through hippocampus and neocortex (RSC, EC brain regions) were captured and a threshold optical density was obtained that discriminated staining from background. Quantification of 4G8 positive A burden is reported as a percentage of immunolabeled area captured (positive pixels divided by total pixels captured). Quantitative image analysis was performed by a single examiner blinded to sample identities. Data are represented as meanSD (n=4 females).

[0083] x. Enzyme-Linked Immunosorbent Assay

[0084] The enzyme-linked immunosorbent assay (ELISA) was performed according to the current inventors' previous methods (37). Soluble A.sub.1-40/42 levels in brain homogenates were analyzed by ELISA using A.sub.1-40/42 ELISA kits (INVITROGEN, Grand Island, N.Y.) in accordance with manufacturer's instructions. Data are represented as meanSD of A.sub.1-40/42 (ng/mg of total protein).

[0085] xi. Monocyte Phagocytosis Assay

[0086] Monocytes were acquired as described earlier from both HUCBCs and aged human blood cells (from senior adults over 70 years old). These cells were further characterized for cell surface CD14.sup.+ and APP biomarkers using flow cytometry analysis. Phagocytosis of A was conducted as previously described (52). Briefly, primary HUCBC-derived monocytes (CB-M) and aged human blood cell-derived monocytes (aged BC-M) were incubated with 1 M FITC-A.sub.1-42 for 1 hour in the absence or presence of sAPP (100 ng/ml), scavenger receptor class A ligand (SR-A) or unlabeled A (naked Ab.sub.42). Both extracellular and cell-associated FITC-A.sub.1-42 from cellular supernatants and lysates were quantified using fluorometric analysis to determine mean fluorescence value for each sample as previously described (53). For each condition, relative fold change values were calculated as: mean fluorescence value for each sample at 37 C./mean fluorescence value for each sample at 4 C. In all of the conditions, an additional control without cells was carried out to account for nonspecific adherence of A to the plastic surface of culture plates and the mean values were normalized to these controls. Monocytes were then fixed and imaged in independent channels using a confocal microscope equipped with Normarski optics.

[0087] xii. Cell Culture and Immunoprecipitation

[0088] Chinese Hamster ovary (CHO) cells overexpressing either WT human APP (CHO/APPwt) or Swedish mutant APP (APPswe) were donated by Dr. Stefanie Hahn and Dr. Sascha Weggen (University of Heinrich Heine, Dsseldorf, Germany). These cells were cultured for 3 hours and then the conditioned media were collected, immunoprecipitated using an anti-A.sub.17-26 monoclonal antibody (4G8), and then analyzed by WB using 22C11 or 6E10. Alternatively, the conditioned media were immunoprecipitated with 22C11 and then analyzed by WB using 6E10. For the parallel heterodimerization study, truncated sAPP peptide was incubated with synthesized A.sub.1-42, immunoprecipated with 4G8 and analyzed by WB using 82E1 or 22C11. In addition, CHO/APPswe-derived conditioned media were collected, immunoprecipitated with 4G8 and then analyzed by WB using 82E1) or 22C11).

[0089] xiii. Statistical Analysis

[0090] All data were presented as meanSEM or meanSD and normally distributed. For the RAWM test, the one-way analysis of variance (ANOVA) followed by post-hoc LSD test was performed to compare differences between groups. For the rotarod test, data were analyzed by ANOVA followed by post-hoc Bonferroni test. For A burden as well as both soluble and insoluble A.sub.1-40/42, a t-test for independent samples followed by a post hoc Bonferroni was used to determine the significant difference between each MD-CB-, WCB-, CB-M-, and PBS-treated group. A P value of <0.05 was considered significant. All analyses were performed using the Statistical Package for the Social Sciences (SPSS), release 18.0 (IBM, Armonk, N.Y.).

[0091] V. Results

[0092] i. Characterization of Purified Human Umbilical Cord Blood-Derived Monocytes

[0093] CD14.sup.+ monocytes were isolated from HUCBCs using a MACS Miltenyi biotec CD14.sup.+ MicroBeads human kit via positive selection and then characterized by FACS analysis. Prior to enrichment, there was a 13% CD14.sup.+ monocyte population (FIG. 1A, upper panel), whereas after positive selection, the population increased to 95% (FIG. 1A, lower panel). HUCBC-derived monocytes were further investigated for surface and full-length APP using 6E10 and pAb751/770 antibodies respectively. Antibody 6E10 recognizes total APP, A, and -CTF, while pAb751/770 antibody specifically recognizes full-length APP. Unfractionated HUCBCs and purified CD14.sup.+ monocytes were 48.0% and 93.8% positive for surface APP (FIG. 1B), respectively. Conversely, pAb751/770 antibody detected only 0.98% and 3% full length APP in unfractionated HUCBCs and purified CD14+ monocytes, respectively, indicating full-length APP may have been truncated (FIG. 1C). To further confirm these data, HUCBCs and HUCBC-derived monocyte lysates were analyzed by Western blot (WB) analysis, indicating that HUCBC-derived monocytes express dramatically more total APP than the whole HUCBCs. The pAb751/770 antibody did not detect any band in both whole HUCBCs and HUCBC-derived monocytes fractions (FIG. 1D).

[0094] ii. Short Term (Two-Month) Administration of HUCBC-Derived Monocytes Improves Learning, Memory and Motor Function in PSAPP and WT Mice

[0095] To investigate whether HUCBC-derived monocytes could improve locomotive and cognitive function, PBS, whole HUCBCs (WCB), HUCBC-derived monocytes (CB-M), or monocyte-deficient HUCBC (MD-CB) was administered intravenously in PSAPP and control (aged-matched WT) mice over a two-month time period and then subjected them to rotarod and RAWM testing. (FIG. 2A). Beginning with the block 2 trial, CB-M- and WCB-treated PSAPP mice showed significantly fewer errors in RAWM than PBS and MD-CB-treated PSAPP mice (FIG. 2B). **P<0.01 versus PBS-PSAPP mice). Likewise, WCB- and CB-M-treated WT mice located the target with significantly fewer errors than PBS-treated WT mice during blocks 3 to 5 and 8 (*P<0.05, **P<0.01 versus PBS-WT and MD-CB-WT littermates). Interestingly, MD-CB-treated PSAPP mice were cognitively inflexible and MD-CB treated WT mice learned less at block 6 and 7 when compared to their PBS-treated WT littermates (FIG. 2B). FIG. 2C shows significantly higher coordination and balance in CB-M compared to PBS, WCB, or MD-CB treated PSAPP and WT mice. Notably, increased latency to fall over time appeared standard for all mice, while CB-M-treated PSAPP and WT mice displayed overall greater latency to fall. This signified that CB-M-treated PSAPP and WT mice developed enhanced coordination and balance abilities over PBS-treated PSAPP and WT mice.

[0096] iii. Long Term (Four-Month) Administration of HUCBC-Derived Monocytes Improves Learning, Memory, and Motor Function in PSAPP and WT Mice

[0097] To investigate whether long term (four-month) monocyte administration improves learning, memory, and motor functions, PBS, whole HUCBCs (WCB), HUCBC-derived monocytes (CB-M), or monocyte-deficient HUCBC (MD-CB) was administered intravenously in PSAPP and control (aged-matched WT) mice over a four-month time period. The behavioral data at 4-month of each treatment were reminiscent of the two-month treatment results (FIGS. 3A-3C). In the RAWM, CB-M- and WCB-treated PSAPP mice showed significantly fewer errors (blocks 2 to 5 on day 1; blocks 6 to 10 on day 2; *P<0.05 and **P<0.01) than all other groups. CB-M and WCB-treated WT mice likewise showed significantly fewer errors in blocks 4, 5 and 9, compared to other groups. Surprisingly, PBS-treated WT mice showed better performance than the MD-CB-treated group in blocks 3, 7, 9, and 10 (FIG. 3B). These findings were further reinforced using the open pool platform swim test to assess whether animals possessed the motor skills sufficient to complete the water maze tasks. Data indicate both two and four-month CB-M-treatment outperformed PBS-treatment of PSAPP and WT mice at short and long term treatment periods (data not shown).

[0098] Rotarod data show that WCB- and CB-M-treated PSAPP and WT mice displayed superior coordination and advanced to the point of sustaining their position on the rod for the entire trial time of 5 minutes (FIG. 3C; day 2), compared to both PBS-treated PSAPP and WT groups (*P<0.05, **P<0.01 versus PBS-PSAPP or WT mice).

[0099] iv. HUCBC-Derived Monocytes Markedly Reduce A Deposits

[0100] To investigate whether HUCBC-derived monocytes could reduce amyloid pathology, the brains of each mouse were investigated after four different treatments (i.e., PBS, whole HUCBCs (WCB), HUCBC-derived monocytes (CB-M), or monocyte-deficient HUCBC (MD-CB) treatments). WCB- and CB-M-treated PSAPP mice showed reduced amyloid plaques in hippocampus (H), retrosplenial cortex (RSC), and entorhinal (EC) regions as compared with PBS- and MD-CB-treated mice using 4G8 immunohistochemical staining (FIG. 4A). Quantitative image analysis shows that percentage of plaques in the H region in CB-M and WCB treated groups was significantly less than PBS- and MD-CB groups (FIG. 4B, upper panel, meanSD, n=4).

[0101] In addition, brain homogenates from the four-month treatment groups were measured for both soluble A.sub.1-40 and A.sub.1-42 levels by ELISA. WCB- and CB-M-treated PSAPP mice showed significantly decreased levels of both soluble A.sub.1-40 and A.sub.1-42 compared to PBS and MD-CB-treated group (FIG. 4C, middle and lower panels, meanSD, n=4). The two-month treatment resulted in similar outcomes (data not shown).

[0102] v. A Phagocytosis by Aged and Cord Blood Cell-Derived Monocytes

[0103] Since phagocytosis by monocytes may be a possible pathway for A clearance from the brain (31,14), it was hypothesized that HUCBC-derived monocytes might phagocytose A HUCBC-derived monocytes (CB-M) and aged human blood cell-derived monocytes (Aged BC-M) were cultured with FITC-A.sub.1-42 for 1 h in the presence or absence of sAPP (100 ng/mL), scavenger receptor class A ligand (SR-A ligand) or unlabeled A.sub.1-42 (Naked A.sub.1-42). Extracellular (FIG. 5A, upper panel) and cell-associated (lower panel) FITC-A.sub.1-42 was then measured from supernatants and lysates respectively using a fluorimeter.

[0104] Data are represented as relative mean fluorescence (meanSD) for each sample at 37 C. divided by mean fluorescence at 4 C. (n=4 for each condition) (*P<0.05, **P<0.01, ***P<0.001 versus aged BC-M). A internalization was reflected by the level of cell-associated FITC-A A.sub.1-42. Interestingly, CB-M internalized A much more than aged CB-M, while sAPP pretreatment (100 ng/ml) enhanced A internalization by aged BC-M. SR-A ligand reduced A internalization by aged CB-M during sAPP treatment, suggesting that SR-A is a primary cell surface receptor accounting for A internalization by these cells. Naked A.sub.1-42 reduced A internalization by HUCBC-M by competitive inhibition.

[0105] Primary monocytes were then fixed and imaged using confocal microscopy equipped with Normarski optics (FIG. 5B). Merged image showed significant A.sub.42 internalization inside the cytoplasm of CB-M as shown by most of the green fluorescence localized inside the cytoplasmic compartment (left upper panel) while aged CB-M showed much less FITC-A.sub.1-42 internalization (left lower panel). Treatment of aged CB-M with sAPP showed significant increase of A.sub.1-42 internalization in the cytoplasm by these cells (right upper panel) while SR-A ligand reduced this effect (right middle panel). As expected, competition by naked A.sub.1-42 significantly decreased FITC-A.sub.1-42 internalization by CB-M (left middle panel).

[0106] vi. In Vitro Heterodimerization sAPP with A

[0107] In this study, it was shown that sAPP treatment improves A phagocytosis by aged blood monocytes. It is known that APP undergoes homodimerization at the cell surface, while sAPP disrupts this homodimerization by binding with APP, thereby preventing starvation-induced cell death (18)]. It was hypothesized that sAPP might also form a heterodimer with A, which is then internalized inside the monocytes. To prove sAPP/A heterodimerization, 3-hour cultured conditioned media of CHO/APPwt or CHO/APPswe cells were immunoprecipitated with anti-A.sub.17-27 antibody (4G8), followed by WB detection using either anti-A.sub.1-16 antibody (6E10) (FIG. 6A, left panel) or anti-APP N-terminal antibody (22C11) (FIG. 6A, right panel). The 22C11 blot showed only the sAPP band (100 kDa), while the 6E10 blot showed both A (4 kDa) and sAPP (100 kDa). Moreover, immunoprecipitation with 22C11, followed by WB detection using 6E10 showed both A (4 kDa) and sAPP (100 kDa) bands (FIG. 6B). Taken together, these data suggest a possible sAPP/A heterodimerization in the cell culture system.

[0108] vii. sAPP/A Heterodimerization at APP.sub.672-687 (A.sub.1-16) Region

[0109] To investigate whether APP.sub.672-687 region is responsible for sAPP/A heterodimerization, truncated sAPP was incubated with synthetic A.sub.1-42 (FIG. 7A), immunoprecipitated with 4G8, and then analyzed by WB detection using either anti-A.sub.1-16 antibody (82E1) (FIG. 7B) or anti-APP N-terminal antibody (22C11) (FIG. 7C). In parallel, CHO/APPswe conditioned media received the same treatments as a negative control. Truncated sAPP incubated with synthetic A.sub.1-42 showed two attached bands with the presence of not only A.sub.1-42 (4 kDa, upper band) but also truncated sAPP (4 kDa, lower band) (FIG. 7B), while CHO/APPswe conditioned media showed only a single band for A.sub.1-42 (4 kDa). In addition, CHO/APPswe conditioned media clearly show one band for sAPP (100 kDa) while truncated sAPP incubated with synthetic A.sub.1-42 clearly shows the presence of truncated sAPP (4 kDa) in the same blot. The presence of sAPP was substantiated by 6E10 WB (data not shown).

C. DISCUSSION AND CONCLUSION

[0110] The findings of this study suggest that peripheral administration of HUCBC-derived monocytes can improve hippocampal dependent learning, memory, and motor function in transgenic PSAPP mice. Histological and biochemical analyses of brain tissue reveal that both short (two-month) and long term (four-month) administration of HUCBC-monocytes reduces amyloid pathology as well as soluble and insoluble A in the brain.

[0111] Confocal microscopy of culture data clearly show that the phagocytic capacity of aged monocytes decreased significantly and was restored by sAPP treatment (FIGS. 5A-5B), indicating that this protein might have an important therapeutic role in reducing A from the brain parenchyma. Furthermore, the lower phagocytic capacity of aged blood monocytes could be explained by significantly less APP surface expression in aged blood monocytes and therefore correspondingly much lower sAPP secretion than HUCBC-derived monocytes (shown in FIGS. 5A-5B). It has been shown that the SR-A receptor binds with A and promotes internalization and clearance (22,50,16) and microglial expression of SR-A increase surrounding human brain plaques area (8).

[0112] The most intriguing part of this study was to identify one of the plausible mechanisms involved in A phagocytosis by monocytes. Confocal microscopy and immunoprecipitation technique show that sAPP binds with A.sub.42 species at the cell surface which promote internalization of A peptide inside the monocyte's cytoplasm. It was hypothesized that heterodimerization of sAPP/A could be a plausible mechanism by which monocytes or peripheral macrophages reduce amyloid burden from brain parenchyma. The in vitro experiment showed that the APP.sub.672-687 (A.sub.1-16) region is responsible for sAPP/A heterodimerization. Many researchers have emphasized that size of A aggregates is crucial for internalization. Weltzien et al. found that smaller aggregates internalized efficiently but larger aggregates usually spend more time on the monocyte's cell surface (45). Thus, the physical limit of A aggregated mass size should be considered for phagocytosis and inflammation aggravation. In sum, it was found that HUCBC-monocytes can be a novel therapeutic option in AD.

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[0167] All referenced publications are incorporated herein by reference in their entirety. Furthermore, where a definition or use of a term in a reference, which is incorporated by reference herein, is inconsistent or contrary to the definition of that term provided herein, the definition of that term provided herein applies and the definition of that term in the reference does not apply.

[0168] The advantages set forth above, and those made apparent from the foregoing description, are efficiently attained. Since certain changes may be made in the above construction without departing from the scope of the invention, it is intended that all matters contained in the foregoing description or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.

[0169] It is also to be understood that the following claims are intended to cover all of the generic and specific features of the invention herein described, and all statements of the scope of the invention that, as a matter of language, might be said to fall therebetween.