A system and method for nonsurgical penile girth enhancement. Hydro-dissection creates a space along a length of the penis between Buck's Fascia and Darte's fascia. The filler material, such as hyaluronic acid, is injected into the space created and is modeled after injection. During the same procedure or a later procedure, additional spaces can be created and injected with the filler material, until the desired girth is obtained. The amount of filler material injected during any given procedure is limited to avoid challenging the lymphatics of the penis. By staging the girth enhancing injections, the risk of penile granulomas can be minimized, if not eliminated.

The present invention relates to a method for producing a cell population comprising myocardium-committed cells that differentiate into and survive as myocardial cells under a myocardial tissue environment. Specifically, the method is characterized in that adipose-tissue-derived multi-lineage/multi-potent progenitor cells are cultured in the presence of a polyamine. The present invention further relates to a cell population comprising the myocardium-committed cells, a cell preparation comprising the cell population, or a cell sheet. The present invention further relates to a method for treating a heart disease, which comprises administering the cell population to a subject.

Described herein are compositions comprising decellularized extracellular matrix derived from skeletal muscle or other suitable tissue, and therapeutic uses thereof. Methods for treating, repairing or regenerating defective, diseased, damage, ischemic, ulcer cells, tissues or organs in a subject preferably a human, with diseases, such as PAD and CLI, using a decellularized extracellular matrix of the invention are provided. Methods of preparing culture surfaces and culturing cells with absorbed decellularized extracellular matrix are provided.

Described herein are compositions comprising decellularized extracellular matrix derived from skeletal muscle or other suitable tissue, and therapeutic uses thereof. Methods for treating, repairing or regenerating defective, diseased, damage, ischemic, ulcer cells, tissues or organs in a subject preferably a human, with diseases, such as PAD and CLI, using a decellularized extracellular matrix of the invention are provided. Methods of preparing culture surfaces and culturing cells with absorbed decellularized extracellular matrix are provided.

The present invention relates to an implantable device, in particular for wall repair comprising a reinforcing textile implant having first and second surfaces, a bioadhesive coating to coat said first surface at least in part, said coating comprising at least one ionic, cross-linked bioadhesive polymer selected from among the following polymers: an acrylic acid polymer, methacrylic acid polymer, itaconic acid polymer, maleic acid polymer or maleic anhydride polymer having an adhesive function that can be activated in an aqueous medium.

An embodiment relates to a phenol-modified decellularized muscle tissue-derived extracellular matrix (MEM) for muscle regeneration and a method for preparing same. The phenol group-modified decellularized MEM of the embodiment is characterized by containing components similar to original proteins of muscle tissue for muscle regeneration and forming a hydrogel having a stable porous nanofiber structure through dimerization crosslinking between phenol groups, wherein the hydrogel can effectively treat muscle injury or muscle diseases by being administered or implanted into muscle tissue without causing side effects such as an immune response or liver or kidney dysfunction.

The present provides a biomaterial for repairing biological tissues, the biomaterial comprising: a water-soluble polymer having a reactive functional group A; and a cell having tissue-regenerating capacity and having, on the surface thereof, a reactive functional group B that can covalently bind to the reactive functional group A, wherein the biomaterial presents a hydrogel state when the reactive functional group A covalently binds to the reactive functional group B. Thus, the present invention can provide a biomaterial for repairing biological tissues that can exert excellent effect in repairing biological tissues by utilizing a hydrogel encapsulating cells having tissue-regenerating capacity.

Provided herein are methods of fractionating extracellular matrix (ECM) materials, producing soluble and structural fractions having different immunological activities. Also provided are compositions and devices comprising the fractions. A method of immune modulation also is provided in which an amount of a soluble or structural ECM fraction prepared according to the methods provided herein is administered to a patient in an amount effective to modulate immune function, for example macrophage function.

A method of producing organized skeletal muscle tissue from precursor muscle cells in vitro comprises: (a) providing precursor muscle cells on a support in a tissue media; then (b) cyclically stretching and relaxing the support at least twice along a first axis during a first time period; and then (c) optionally but preferably maintaining the support in a substantially static position during a second time period; and then (d) repeating steps (b) and (c) for a number of times sufficient to enhance the functionality of the tissue formed on the support and/or produce organized skeletal muscle tissue on the solid support from the precursor muscle cells.

The present invention provides an actuator, comprising a fiber and a temperature regulator capable of at least one of heating and cooling the fiber. The fiber is twisted around a longitudinal axis thereof. The fiber is folded so as to have a shape of a cylindrical coil. The fiber is formed of linear low-density polyethylene. The following mathematical formula (I) is satisfied: D/d<1 (I), where D represents a mean diameter of the cylindrical coil; and d represents a diameter of the fiber.