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PMID: 19829375 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Asymmetric centrosome inheritance maintains neural progenitors in the neocortex.

Nature ·Vol. 461 ·No. 7266 ·2009-10-15 ·Pages 947-55

Wang X, Tsai JW, Imai JH, Lian WN, Vallee RB, Shi SH

Abstract

Asymmetric divisions of radial glia progenitors produce self-renewing radial glia and differentiating cells simultaneously in the ventricular zone (VZ) of the developing neocortex. Whereas differentiating cells leave the VZ to constitute the future neocortex, renewing radial glia progenitors stay in the VZ for subsequent divisions. The differential behaviour of progenitors and their differentiating progeny is essential for neocortical development; however, the mechanisms that ensure these behavioural differences are unclear. Here we show that asymmetric centrosome inheritance regulates the differential behaviour of renewing progenitors and their differentiating progeny in the embryonic mouse neocortex. Centrosome duplication in dividing radial glia progenitors generates a pair of centrosomes with differently aged mother centrioles. During peak phases of neurogenesis, the centrosome retaining the old mother centriole stays in the VZ and is preferentially inherited by radial glia progenitors, whereas the centrosome containing the new mother centriole mostly leaves the VZ and is largely associated with differentiating cells. Removal of ninein, a mature centriole-specific protein, disrupts the asymmetric segregation and inheritance of the centrosome and causes premature depletion of progenitors from the VZ. These results indicate that preferential inheritance of the centrosome with the mature older mother centriole is required for maintaining radial glia progenitors in the developing mammalian neocortex.

MeSH Terms
Animals Calcium-Binding Proteins/genetics,metabolism Cell Differentiation Cell Division Cell Lineage Cellular Senescence/physiology Centrioles/physiology Centrosome/physiology Chromosomal Proteins, Non-Histone/genetics,metabolism Cytoskeletal Proteins/deficiency,genetics,physiology Humans Mice Neocortex/cytology,embryology Neurogenesis/physiology Neuroglia/cytology Neurons/cytology Nuclear Proteins/deficiency,genetics,physiology Stem Cells/cytology
Chemicals
Calcium-Binding Proteins Chromosomal Proteins, Non-Histone Cytoskeletal Proteins Nin protein, mouse Nuclear Proteins caltractin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wang Xiaoqun
Developmental Biology Program, Memorial Sloan Kettering Cancer Centre, 1275 York Avenue, New York, New York 10065, USA.
Tsai Jin-Wu
Imai Janice H
Lian Wei-Nan
Vallee Richard B
Shi Song-Hai
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Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2009-10-15
Pages
947-55
Language
English
Region
England
NLM ID
0410462
PMCID
PMC2764320
Subset
IM
Grants
NCI NIH HHS · P30 CA008748 · United States
NIDA NIH HHS · R01 DA024681 · United States
NIDA NIH HHS · R01 DA024681-01A1 · United States
NIDA NIH HHS · R01 DA024681-02 · United States
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