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Int. J. Mol. Sci. 2010, 11(9), 3288-3297; doi:10.3390/ijms11093288
Review

Stem Cells and Neuroprotection: Understanding the Players

Received: 12 July 2010; in revised form: 12 August 2010 / Accepted: 1 September 2010 / Published: 15 September 2010
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Abstract: The use of neuroprotective therapies begs the question of how such therapies could affect preexisting stem cell populations within the host, as well as those introduced through cell-replacement therapy. Multiple mechanisms may mediate stem cell responses to neuroprotectants such as host/donor age and gender, cellular lineage/differentiation status, and mitochondrial dynamics. Current therapeutic sources for stem cells are embryonic, somatic, or induced pluripotent, with very little known about the effects of gender, age, cell type, and mitochondrial dynamics. With the advent of therapies to stimulate and recruit endogenous stem cells or transplant donor cells into damage areas in the hopes of recuperative regeneration of lost neurons, it is important to discuss mechanisms that dictate the winning players in the neuroprotection game. This review will focus on our current understanding of the characteristics of renewing stem cells that may affect neuroprotection.
Keywords: stem cells; neuroprotection; gender specific; telomerase; mitochondria; renewal stem cells; neuroprotection; gender specific; telomerase; mitochondria; renewal
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Pearce, V. Stem Cells and Neuroprotection: Understanding the Players. Int. J. Mol. Sci. 2010, 11, 3288-3297.

AMA Style

Pearce V. Stem Cells and Neuroprotection: Understanding the Players. International Journal of Molecular Sciences. 2010; 11(9):3288-3297.

Chicago/Turabian Style

Pearce, Virginia. 2010. "Stem Cells and Neuroprotection: Understanding the Players." Int. J. Mol. Sci. 11, no. 9: 3288-3297.


Int. J. Mol. Sci. EISSN 1422-0067 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert