The isolation, differentiation, and survival in vivo of multipotent cells from the postnatal rat filum terminale

Document Type

Article

Abstract

Neural stem cells (NSCs) are undifferentiated cells in the central nervous system (CNS) that are capable of self-renewal and can be induced to differentiate into neurons and glia. Current sources of mammalian NSCs are confined to regions of the CNS that are critical to normal function and surgically difficult to access, which limits their therapeutic potential in human disease. We have found that the filum terminale (FT), a previously unexplored, expendable, and easily accessible tissue at the caudal end of the spinal cord, is a source of multipotent cells in postnatal rats and humans. In this study, we used a rat model to isolate and characterize the potential of these cells. Neurospheres derived from the rat FT are amenable to in vitro expansion in the presence of a combination of growth factors. These proliferating, FT-derived cells formed neurospheres that could be induced to differentiate into neural progenitor cells, neurons, astrocytes, and oligodendrocytes by exposure to serum and/or adhesive substrates. Through directed differentiation using sonic hedgehog and retinoic acid in combination with various neurotrophic factors, FT-derived neurospheres generated motor neurons that were capable of forming neuromuscular junctions in vitro. In addition, FT-derived progenitors that were injected into chick embryos survived and could differentiate into both neurons and glia in vivo.

Medical Subject Headings

Animals; Animals, Newborn; Astrocytes (cytology, physiology); Cauda Equina (cytology, physiology); Cell Differentiation; Chick Embryo; Hedgehog Proteins (metabolism, pharmacology); Intercellular Signaling Peptides and Proteins (metabolism, pharmacology); Microinjections; Motor Neurons (cytology, physiology); Multipotent Stem Cells (cytology, drug effects, physiology); Neural Stem Cells (cytology, drug effects, physiology); Neuromuscular Junction (cytology, physiology); Oligodendroglia (cytology, physiology); Primary Cell Culture; Rats; Rats, Sprague-Dawley; Tretinoin (metabolism, pharmacology)

Publication Date

1-1-2013

Publication Title

PloS one

E-ISSN

1932-6203

Volume

8

Issue

6

First Page

e65974

PubMed ID

23762453

Digital Object Identifier (DOI)

10.1371/journal.pone.0065974

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