Functional myelination of neurons
AssigneesUniversity of Maryland, Baltimore, The United States of America as represented by the Department of Veterans Affairs
InventorsThomas Hornyak, Sandeep Joshi
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AssigneesUniversity of Maryland, Baltimore, The United States of America as represented by the Department of Veterans Affairs
InventorsThomas Hornyak, Sandeep Joshi
Estimating the term…
Hair follicle bulge region/LLP region CD34(+) MeSCs can be isolated from mammalian skin bearing hair follicles. These cells are multipotent and retain the ability to differentiate into cells of neural crest lineage, including glia-like cells that express the glial marker Gfap, and are able to express myelin basic protein, and to remyelinate naked (unmyelinated or demyelinated) neuronal processes with a functional, dense myelin sheath. These cells of neural crest lineage can be used to produce a dense myelin sheath on neurons which lack myelin due to genetic defect, trauma, toxin, infection, or disease process. Therefore, embodiments of the invention provide methods for preparing such cells, the cells themselves and compositions containing the cells, as well as methods for using the cells.
A method of producing a functional myelin sheath on one or more neurites of neurons that lack a functional myelin sheath, comprising contacting the neurons with isolated myelin-depositing cells which:
A method of producing a functional myelin sheath on one or more neurites of neurons that lack a functional myelin sheath, comprising contacting the neurons with isolated myelin-depositing cells which:
Dependencies are inferred from the claim text.