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PNAS 97 (18): 10032-10037
Copyright © 2000 by the National Academy of Sciences.
Developmental Biology
Redox state is a central modulator of the balance between
self-renewal and differentiation in a dividing glial
precursor cell
Joel
Smith*,
Ena
Ladi ,
Margot
Mayer-Pröschel , and
Mark
Noble ,§
* Huntsman Cancer Institute, Department of Oncological Sciences,
University of Utah, 2000 N. Medical Drive, Room 4280, Salt Lake City,
UT 84112; Department of Biological Chemistry, UCLA School
of Medicine, Los Angeles, CA 90095; and Center for
Cancer Biology, AAB Institute for Biomedical Sciences, Box 633, University of Rochester, 601 Elmwood Ave, Rochester, NY 14610
Edited by Darwin J. Prockop, MCP Hahnemann University,
Philadelphia, PA, and approved June 14, 2000 (received for review May
9, 2000)
We have discovered that intracellular redox state appears to be a
necessary and sufficient modulator of the balance between self-renewal
and differentiation in dividing oligodendrocyte-type-2 astrocyte
progenitor cells. The intracellular redox state of freshly isolated
progenitors allows prospective isolation of cells with different
self-renewal characteristics. Redox state is itself modulated by
cell-extrinsic signaling molecules that alter the balance between
self-renewal and differentiation: growth factors that promote
self-renewal cause progenitors to become more reduced, while signaling
molecules that promote differentiation cause progenitors to become more
oxidized. Moreover, pharmacological antagonists of the redox effects of
these cell-extrinsic signaling molecules antagonize their effects on
self-renewal and differentiation, indicating that cell-extrinsic
signaling molecules that modulate this balance converge on redox
modulation as a critical component of their effector mechanism.
§
To whom all reprint requests should be addressed.
E-mail: mark_noble{at}urmc.rochester.edu.
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