Spinal Cord-Derived Progenitor Cells are Prevalent and Active
Horner, P.J., A.E.Power, G.Kempermann, H.G.Kuhn,
T.D.Palmer, J. Winkler, L.J.Thal, and F.H. Gage. 2000. Existence
of progenitor cells throughout the intact adult rat spinal cord.
J.Neurosci. 20(6): 2218-2228.
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Adult spinal cord contains NG2-expressing
glial progenitor cells that continue to divide after the period
of post-natal gliagenesis. NG2 is a surface proteoglycan
that thought to be expressed on progenitor cells that are bi-potent,
giving rise to astrocytes and oligodendrocytes. Progenitor cells
are derived from stem cells but typically have reduced self renewal
capacity and differentiation capability. Unlike stem cells, progenitor
cells are rapidly dividing. In the adult spinal cord, glial replacement
is thought to slow down or end shortly after birth. In the above
experiments we analyzed the number of dividing cells in the adult
spinal cord and found there to be significant cell division even
in older age groups. Perhaps most surprising is the finding that
these cells are likely glial progenitor cells because they express
NG2 (A). During cell division these progenitor cells have short
uni- or bipolar processes (C). By 1 day these processes extend and
the cells assume a bipolar shape (B above). By 4 weeks, NG2-expressing
progenitor cells exhibit a complex multipolar morphology reminiscent
of an oligodendrocyte (B below). These findings suggest that the
adult spinal cord harbors highly active progenitor cells that may
be used as a resource for spinal cord repair. In the future, we
must better understand the physiological role for these cells and
how they are altered by injury or degeneration.

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