This disclosure relates to methods of growing cells within a hydrogel scaffold and pressurizing the hydrogel and cells to induce the cells to stretch and differentiation. The disclosed method can include coating a substrate of a bioreactor with a hydrogel and seeding cells onto the hydrogel and/or the substrate. The disclosed method can further include growing the seeded cells into a cell mass and pressurizing the cell mass and the hydrogel within the bioreactor. Pressurizing the cell mass and the hydrogel induces the cell mass and hydrogel to mechanically stretch, thereby inducing hypertrophy and cell alignment.

Various embodiments disclosed relate to conductive graphene matrix-encapsulated cells. A matrix-encapsulated cell includes an encapsulating polymer matrix including a biopolymer and graphene. The matrix-encapsulated cell also includes one or more of the cells encapsulated within the encapsulating polymer, wherein the graphene directly contacts at least some of the cells. The matrix encapsulating the one or more cells is electrically conductive.

The present invention provides substantia nigra organoids on silica iSECnMs and method of producing the same. The present invention also provides method of cell therapy including the substantia nigra organoids on silica iSECnMs. It also provides a method of promoting differentiation of neural stem cells to neurons includes culturing the neural stem cells on a nanostructure having a plurality of nanozigzags or nanohelices fabricated from SiO.sub.2 or TiO.sub.x.

Provided are 3D cell culture scaffolds, 3D nanofiber scaffolds, and edible 3D nanofiber scaffolds for cultured meat. Described is a 3D cell culture scaffold including a plurality of laminated nanofiber layers. Each layer is formed by an array of nanofibers. The diameter of each of the nanofibers in the arrays can have a tunable, predetermined diameter and can be formed from materials including a natural polymer, a synthetic polymer, a biocompatible material, or a combination thereof. Each of the nanofibers in the arrays can have controlled alignment, angle, and spacing from one another. The layers can be spaced by spacer fibers or spacer sheets. The scaffold can have a porosity of about 50% to 99%. Edible 3D scaffolds for cultured meat are also provided where the nanofibers and spacers are edible.

The present invention provides nanostructures for use in proliferation and differentiation of neural stem cells. The present invention also provides method of proliferating and differentiating neural stem cells.

A method of coating a surface with nanoparticles for biological analysis of cells that includes the steps of cleaning the surface with an oxidizing acid, treating the surface with an organosilane, coating the surface with nanoparticles, and then growing cells on the surface coated with the nanoparticles. The surface may be a glass surface, a silica-based surface, a plastic-based surface or a polymer-based surface. The nanoparticles may be gold-based nanomaterials.

Biomimetic grafts or implants coated with an osteogenic extracellular matrix and methods for production and use are described.

Disclosed here is a three-dimensional electronic scaffold, comprising a porous scaffold and a plurality of micro-strain gauges distributed spatially inside the porous scaffold, wherein the micro-strain gauges are adapted to detect contraction force. Also disclosed is a method comprising detecting and mapping intra-tissue cardiac contraction force of one or more cardiac cells or tissues disposed in a three-dimensional electronic scaffold, wherein the three-dimensional electronic scaffold comprises a porous scaffold and a plurality of micro-strain gauges distributed spatially inside the porous scaffold and in contact with the cardiac cells or tissues, and wherein the micro-strain gauges are adapted to detect contraction force of the cardiac cells or tissues.

A system and method for growing and maintaining biological material including producing a protein associated with the tissue, selecting cells associated with the tissue, expanding the cells, creating at least one tissue bio-ink including the expanded cells, printing the at least one tissue bio-ink in at least one tissue growth medium mixture, growing the tissue from the printed at least one tissue bio-ink, and maintaining viability of the tissue.

This invention relates to live cell constructs for in vitro and/or ex vivo production of cultured milk products from mammary cells, methods of producing isolated cultured milk products from mammary cells, bioreactors for producing isolated cultured milk products, and cultured milk products.