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Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke.

Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke. Research Abstract Details 

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  • Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke. Abstract Text:

    rui l zhangRui L Zhang,zheng g zhangZheng G Zhang,cynthia robertsCynthia Roberts,yvonne letourneauYvonne LeTourneau,mei luMei Lu,li zhangLi Zhang,ying wangYing Wang,michael choppMichael Chopp,

    The proportion of neural progenitors that remain in (P fraction) and exit from (Q fraction) the cell cycle determines the degree of neurogenesis. Using S-phase labeling with 5-bromo-2'-deoxyuridine and a double nucleoside analog-labeling scheme, we measured the cell-cycle kinetics of neural progenitors and estimated the proportion of P and Q fractions in the subventricular zone (SVZ) of adult rats subjected to stroke. Stroke increased SVZ cell proliferation, starting 2 days, reaching a maximum 4 and 7 days after stroke. The cell-cycle length (T(C)) of SVZ cells changed dynamically over a period of 2 to 14 days after stroke, with the shortest length of 11 h at 2 days after stroke. The reduction of the T(C) resulted from a decrease of the G(1) phase because the G(2), M, and S phases were unchanged. In addition, during this period, reduction of the G(1) phase was concomitant with an increase in the P fraction, whereas an augmentation of the Q fraction was associated with lengthening of the G(1) phase. Furthermore, approximately 90% of cells that exited the cell cycle were neurons and the population of a pair of dividing daughter cells with a neuronal marker increased from 9% at 2 days to 26% at 14 days after stroke. These data suggest that stroke triggers early expansion of the progenitor pool via shortening the cell-cycle length and retaining daughter cells within the cell cycle, and the lengthening of G(1) leads to daughter cells exiting the cell cycle and differentiating into neurons.Journal of Cerebral Blood Flow & Metabolism (2008) 28, 602-611; doi:10.1038/sj.jcbfm.9600556; published online 10 October 2007.

    Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke. Publishing Authors By Initials

    rl zhangRL Zhang,zg zhangZG Zhang,c robertsC Roberts,y letourneauY LeTourneau,m luM Lu,l zhangL Zhang,y wangY Wang,m choppM Chopp,

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    Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of cerebral blood flow and metabolism : of

    VOLUME: 28

    Page Numbers: 602-11

    Journal Abbreviation: J. Cereb. Blood Flow Metab.

    ISSN: 0271-678X

    DAY: 10

    MONTH: 10

    YEAR: 2007

    Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke. Information

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    LANGUAGE: eng

    NlmUniqueID: 8112566

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    Grant and Affiliation Information for Lengthening the G(1) phase of neural progenitor cells is concurrent with an increase of symmetric neuron generating division after stroke.

    AFFILIATION: 1Department of Neurology, Henry Ford Health System, Detroit, Michigan, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Cereb Blood Flow Metab

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