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不对称的中心体遗传维持新皮质中的神经祖细胞。

Asymmetric centrosome inheritance maintains neural progenitors in the neocortex.

作者信息

Wang Xiaoqun, Tsai Jin-Wu, Imai Janice H, Lian Wei-Nan, Vallee Richard B, Shi Song-Hai

机构信息

Developmental Biology Program, Memorial Sloan Kettering Cancer Centre, 1275 York Avenue, New York, New York 10065, USA.

出版信息

Nature. 2009 Oct 15;461(7266):947-55. doi: 10.1038/nature08435.

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.

摘要

放射状胶质细胞祖细胞的不对称分裂在发育中的新皮质的脑室区(VZ)同时产生自我更新的放射状胶质细胞和分化细胞。分化细胞离开VZ以构成未来的新皮质,而自我更新的放射状胶质细胞祖细胞留在VZ进行后续分裂。祖细胞及其分化后代的不同行为对新皮质发育至关重要;然而,确保这些行为差异的机制尚不清楚。在这里,我们表明不对称的中心体遗传调节胚胎小鼠新皮质中自我更新的祖细胞及其分化后代的不同行为。分裂的放射状胶质细胞祖细胞中的中心体复制产生一对具有不同年龄母中心粒的中心体。在神经发生的高峰期,保留旧母中心粒的中心体留在VZ,并优先被放射状胶质细胞祖细胞继承,而含有新母中心粒的中心体大多离开VZ,并在很大程度上与分化细胞相关。去除九蛋白(一种成熟的中心粒特异性蛋白)会破坏中心体的不对称分离和遗传,并导致祖细胞从VZ过早耗尽。这些结果表明,在发育中的哺乳动物新皮质中,具有成熟的旧母中心粒的中心体的优先遗传是维持放射状胶质细胞祖细胞所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c513/2764320/c1408d09e2fc/nihms139941f1.jpg

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