초록 ▼

The invention features a method for generating new tissue by obtaining a liquid hydrogel-cell composition including a hydrogel and tissue precursor cells; delivering the liquid hydrogel-cell composition into a permeable, biocompatible support structure; and allowing the liquid hydrogel-cell composit

The invention features a method for generating new tissue by obtaining a liquid hydrogel-cell composition including a hydrogel and tissue precursor cells; delivering the liquid hydrogel-cell composition into a permeable, biocompatible support structure; and allowing the liquid hydrogel-cell composition to solidify within the support structure and the tissue precursor cells to grow and generate new tissue. The invention also features a tissue forming structure including a permeable, biocompatible support structure having a predetermined shape that corresponds to the shape of desired tissue; and a hydrogel-cell composition at least partially filling the support structure, wherein the hydrogel-cell composition includes a hydrogel and tissue precursor cells. The new tissue forming structure can be used in new methods to generate various tissues (e.g., to treat defective tissue) including new bone, cartilage, and nervous tissue such as spinal cord tissue. The invention also new isolated nervous system stem cells.

대표청구항 ▼

What is claimed is: 1. A population of isolated mammalian adult undifferentiated cells obtainable following digestion of dissociated neural, endocrine or neuroendocrine tissue with trypsin, in combination with a support material for implantation, wherein the structure of the support material guides

What is claimed is: 1. A population of isolated mammalian adult undifferentiated cells obtainable following digestion of dissociated neural, endocrine or neuroendocrine tissue with trypsin, in combination with a support material for implantation, wherein the structure of the support material guides the development and shape of new tissue from the cell population and resists external compressive and tensile stresses from the environment and surrounding tissues. 2. The undifferentiated cell population of claim 1, wherein the undifferentiated cell population is isolated from adrenal gland or pancreas tissue. 3. The undifferentiated cell population of claim 1 isolated by digestion of the tissue with trypsin, washing the cells with buffer and isolation of the cells by centrifugation sufficient to separate the undifferentiated intact cells from the buffer. 4. The undifferentiated cell population of claim 1 isolated from the hypothalamus, pituitary, parathyroid, or thyroid. 5. The undifferentiated cell population of claim 1 isolated from along the intestinal tract or the aorta. 6. The undifferentiated cell population of claim 1 wherein the tissue is digested under conditions equivalent to 0.05 % trypsin at 37�� C. for five minutes. 7. The undifferentiated cell population of claim 1 further comprising a hydrogel. 8. The undifferentiated cell population of claim 7 wherein the support material is selected from the group consisting of sponges, foam, coral, rigid inorganic, ceramic, or metal structures having internal pores, a honeycomb structure made from titanium, a skeleton of struts, a mesh of interwoven polymer fibers, and a network of metal, inorganic, ceramic, or plastic rods. 9. The undifferentiated cell population of claim 1 wherein the support material comprises a polymeric support structure. 10. The undifferentiated cell population of claim 1 further comprising factors selected from the group consisting of growth factors, nutrients, and drugs. 11. The undifferentiated cell population of claim 7 or 8 wherein the cell population in combination with a support material and support structure are useful for spinal cord repair.