INSERM U682, Strasbourg, France.
Cell Adh Migr. 2011 Nov-Dec;5(6):480-9. doi: 10.4161/cam.5.6.19191.
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.
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。