Sakurai T, Lustig M, Babiarz J, Furley A J, Tait S, Brophy P J, Brown S A, Brown L Y, Mason C A, Grumet M
W.M. Keck Center for Collaborative Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.
J Cell Biol. 2001 Sep 17;154(6):1259-73. doi: 10.1083/jcb.200104122.
The structurally related cell adhesion molecules L1 and Nr-CAM have overlapping expression patterns in cerebellar granule cells. Here we analyzed their involvement in granule cell development using mutant mice. Nr-CAM-deficient cerebellar granule cells failed to extend neurites in vitro on contactin, a known ligand for Nr-CAM expressed in the cerebellum, confirming that these mice are functionally null for Nr-CAM. In vivo, Nr-CAM-null cerebella did not exhibit obvious histological defects, although a mild size reduction of several lobes was observed, most notably lobes IV and V in the vermis. Mice deficient for both L1 and Nr-CAM exhibited severe cerebellar folial defects and a reduction in the thickness of the inner granule cell layer. Additionally, anti-L1 antibodies specifically disrupted survival and maintenance of Nr-CAM-deficient granule cells in cerebellar cultures treated with antibodies. The combined results indicate that Nr-CAM and L1 play a role in cerebellar granule cell development, and suggest that closely related molecules in the L1 family have overlapping functions.
结构相关的细胞粘附分子L1和Nr-CAM在小脑颗粒细胞中具有重叠的表达模式。在此,我们使用突变小鼠分析了它们在颗粒细胞发育中的作用。Nr-CAM缺陷型小脑颗粒细胞在体外与contactin(小脑表达的Nr-CAM的已知配体)接触时无法延伸神经突,证实这些小鼠在功能上缺失Nr-CAM。在体内,Nr-CAM缺失的小脑未表现出明显的组织学缺陷,尽管观察到几个叶有轻度尺寸减小,最明显的是蚓部的IV叶和V叶。L1和Nr-CAM双缺陷的小鼠表现出严重的小脑叶缺陷以及内颗粒细胞层厚度减小。此外,抗L1抗体在用抗体处理的小脑培养物中特异性破坏了Nr-CAM缺陷型颗粒细胞的存活和维持。综合结果表明,Nr-CAM和L1在小脑颗粒细胞发育中起作用,并表明L1家族中密切相关的分子具有重叠功能。