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本文引用的文献

1
Laminin α1 is essential for mouse cerebellar development.层粘连蛋白α1 对于小鼠小脑的发育至关重要。
Matrix Biol. 2012 Jan;31(1):17-28. doi: 10.1016/j.matbio.2011.09.002. Epub 2011 Sep 29.
2
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.深度测序揭示 50 个隐性认知障碍的新基因。
Nature. 2011 Sep 21;478(7367):57-63. doi: 10.1038/nature10423.
3
The high mitotic count detected by phospho-histone H3 immunostain does not alter the benign behavior of angiocentric glioma.免疫组化磷酸化组蛋白 H3 检测到的高有丝分裂计数并不会改变血管中心性胶质瘤的良性行为。
Brain Tumor Pathol. 2012 Jan;29(1):68-72. doi: 10.1007/s10014-011-0062-0. Epub 2011 Sep 3.
4
Role of laminins in physiological and pathological angiogenesis.层粘连蛋白在生理性和病理性血管生成中的作用。
Int J Dev Biol. 2011;55(4-5):455-65. doi: 10.1387/ijdb.103223ps.
5
Organogenesis of the kidney glomerulus: focus on the glomerular basement membrane.肾脏肾小球的发生:关注肾小球基底膜。
Organogenesis. 2011 Apr-Jun;7(2):75-82. doi: 10.4161/org.7.2.15275. Epub 2011 Apr 1.
6
Coordination between extrinsic extracellular matrix cues and intrinsic responses to orient the centrosome in polarizing cerebellar granule neurons.外在细胞外基质线索与内在反应之间的协调作用,使小脑颗粒神经元中的中心体定向极化。
J Neurosci. 2010 Feb 17;30(7):2755-66. doi: 10.1523/JNEUROSCI.4218-09.2010.
7
Mutations in Lama1 disrupt retinal vascular development and inner limiting membrane formation.Lama1 突变会破坏视网膜血管发育和内界膜形成。
J Biol Chem. 2010 Mar 5;285(10):7697-711. doi: 10.1074/jbc.M109.069575. Epub 2010 Jan 4.
8
Recent developments in the understanding of astrocyte function in the cerebellum in vivo.小脑星形胶质细胞功能的体内研究的最新进展。
Cerebellum. 2010 Sep;9(3):264-71. doi: 10.1007/s12311-009-0139-z.
9
Defining the role of laminin-332 in carcinoma.定义层粘连蛋白-332 在癌中的作用。
Matrix Biol. 2009 Oct;28(8):445-55. doi: 10.1016/j.matbio.2009.07.008. Epub 2009 Aug 15.
10
Developmental and pathogenic mechanisms of basement membrane assembly.基底膜组装的发育和致病机制。
Curr Pharm Des. 2009;15(12):1277-94. doi: 10.2174/138161209787846766.

层粘连蛋白α1 链在小脑发育中的功能作用。

Functional role of laminin α1 chain during cerebellum development.

机构信息

INSERM U682, Strasbourg, France.

出版信息

Cell Adh Migr. 2011 Nov-Dec;5(6):480-9. doi: 10.4161/cam.5.6.19191.

DOI:10.4161/cam.5.6.19191
PMID:22274713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3277781/
Abstract

We had developed a conditional Laminin α 1 knockout-mouse model (Lama1(cko)) bypassing embryonic lethality of Lama1 deficient mice to study the role of this crucial laminin chain during late developmental phases and organogenesis. Here, we report a strong defect in the organization of the adult cerebellum of Lama1(cko) mice. Our study of the postnatal cerebellum of Lama1(cko) animals revealed a disrupted basement membrane correlated to an unexpected excessive proliferation of granule cell precursors in the external granular layer (EGL). This was counteracted by a massive cell death occurring between the postnatal day 7 (P7) and day 20 (P20) resulting in a net balance of less cells and a smaller cerebellum. Our data show that the absence of Lama1 has an impact on the Bergmann glia scaffold that aberrantly develops. This phenotype is presumably responsible for the observed misplacing of granule cells that may explain the overall perturbation of the layering of the cerebellum and an aberrant folia formation.

摘要

我们开发了一种条件性层粘连蛋白α 1 敲除鼠模型(Lama1(cko)),绕过 Lama1 缺陷型小鼠的胚胎致死性,以研究这种关键层粘连蛋白链在晚期发育阶段和器官发生中的作用。在这里,我们报告了 Lama1(cko)小鼠成年小脑组织的严重缺陷。我们对 Lama1(cko)动物出生后的小脑进行研究,发现其基底膜组织紊乱,与外颗粒层(EGL)中颗粒细胞前体异常增殖有关。这被出生后第 7 天(P7)至第 20 天(P20)之间发生的大量细胞死亡所抵消,导致净细胞数减少和小脑体积缩小。我们的数据表明,缺乏 Lama1 对 Bergmann 神经胶质支架有影响,该支架异常发育。这种表型可能是导致观察到的颗粒细胞错位的原因,这可以解释小脑的整体分层和叶状结构异常。