Gerke Peter, Benzing Thomas, Höhne Martin, Kispert Andreas, Frotscher Michael, Walz Gerd, Kretz Oliver
Renal Division, University of Freiburg, D-79104 Freiburg, Germany.
J Comp Neurol. 2006 Oct 1;498(4):466-75. doi: 10.1002/cne.21064.
Formation, differentiation, and plasticity of synapses require interactions between pre- and postsynaptic partners. Recently, it was shown that the transmembrane immunoglobulin superfamily protein SYG-1 is required for providing synaptic specificity in C. elegans. However, it is unclear whether the mammalian orthologs of SYG-1 are also involved in local cell interactions to determine specificity during synapse formation. We used in situ hybridization, immunohistochemistry, and immunogold electron microscopy to study the temporal and spatial expression of Neph1 and Neph2 in the developing and adult mouse brain. Both proteins show similar patterns with neuronal expression starting around embryonic days 12 and 11, respectively. Expression is strongest in areas of high migratory activity. In the adult brain, Neph1 and Neph2 are predominantly seen in the olfactory nerve layer and the glomerular layer of the olfactory bulb, in the hippocampus, and in Purkinje cells of the cerebellum. At the ultrastructural level, Neph1 and Neph2 are detectable within the dendritic shafts of pyramidal neurons. To a lesser extent, there is also synaptic localization of Neph1 within the stratum pyramidale of the hippocampal CA1 and CA3 region on both pre- and postsynaptic sites. Here it colocalizes with the synaptic scaffolder calmodulin-associated serin/threonin kinase (CASK), and both Neph1 and Neph2 interact with the PDZ domain of CASK via their cytoplasmic tail. Our results show that Neph proteins are expressed in the developing nervous system of mammals and suggest that these proteins may have a conserved function in synapse formation or neurogenesis.
突触的形成、分化和可塑性需要突触前和突触后伙伴之间的相互作用。最近的研究表明,跨膜免疫球蛋白超家族蛋白SYG-1是秀丽隐杆线虫中提供突触特异性所必需的。然而,尚不清楚SYG-1的哺乳动物直系同源物是否也参与局部细胞相互作用以在突触形成过程中确定特异性。我们使用原位杂交、免疫组织化学和免疫金电子显微镜来研究Neph1和Neph2在发育中和成年小鼠大脑中的时空表达。这两种蛋白显示出相似的模式,神经元表达分别在胚胎第12天和第11天左右开始。在高迁移活性区域表达最强。在成年大脑中,Neph1和Neph2主要见于嗅神经层和嗅球的肾小球层、海马以及小脑的浦肯野细胞。在超微结构水平上,Neph1和Neph2可在锥体神经元的树突干内检测到。在较小程度上,Neph1在海马CA1和CA3区域的锥体层的突触前和突触后位点也有突触定位。在这里它与突触支架钙调蛋白相关丝氨酸/苏氨酸激酶(CASK)共定位,并且Neph1和Neph2都通过其细胞质尾巴与CASK的PDZ结构域相互作用。我们的结果表明,Neph蛋白在哺乳动物发育中的神经系统中表达,并表明这些蛋白可能在突触形成或神经发生中具有保守功能。