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神经细胞膜糖蛋白GPM6a与细胞间细胞黏附分子ICAM5对神经元形态发生的联合加性效应。

Combined additive effects of neuronal membrane glycoprotein GPM6a and the intercellular cell adhesion molecule ICAM5 on neuronal morphogenesis.

作者信息

Gutiérrez Fuster R, León A, Aparicio G I, Brizuela Sotelo F, Scorticati C

机构信息

Instituto de Investigaciones Biotecnológicas, Universidad Nacional de San Martín (UNSAM)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), San Martín, Buenos Aires, Argentina.

Escuela de Bio y Nanotecnologías (EByN), Universidad Nacional de San Martín, San Martín, Buenos Aires, Argentina.

出版信息

J Neurochem. 2025 Jan;169(1):e16231. doi: 10.1111/jnc.16231. Epub 2024 Oct 1.

Abstract

The mechanisms underlying neuronal development and synaptic formation in the brain depend on intricate cellular and molecular processes. The neuronal membrane glycoprotein GPM6a promotes neurite elongation, filopodia/spine formation, and synapse development, yet its molecular mechanisms remain unknown. Since the extracellular domains of GPM6a (ECs) command its function, we investigated the interaction between ICAM5, the neuronal member of the intercellular adhesion molecule (ICAM) family, and GPM6a's ECs. Our study aimed to explore the functional relationship between GPM6a and ICAM5 in hippocampal culture neurons and cell lines. Immunostaining of 15 days in vitro (DIV) neurons revealed significant co-localization between endogenous GPM6a clusters and ICAM5 clusters in the dendritic shaft. These results were further corroborated by overexpressing GPM6a and ICAM5 in N2a cells and hippocampal neurons at 5 DIV. Moreover, results from the co-immunoprecipitations and cell aggregation assays prove the cis and trans interaction between both proteins in GPM6a/ICAM5 overexpressing HEK293 cells. Additionally, GPM6a and ICAM5 overexpression additively enhanced neurite length, the number of neurites in N2a cells, and filopodia formation in 5 DIV neurons, indicating their cooperative role. These findings highlight the dynamic association between GPM6a and ICAM5 during neuronal development, offering insights into their contributions to neurite outgrowth, filopodia formation, and cell-cell interactions.

摘要

大脑中神经元发育和突触形成的潜在机制依赖于复杂的细胞和分子过程。神经元膜糖蛋白GPM6a促进神经突伸长、丝状伪足/棘突形成和突触发育,但其分子机制仍不清楚。由于GPM6a的细胞外结构域(ECs)决定其功能,我们研究了细胞间粘附分子(ICAM)家族的神经元成员ICAM5与GPM6a的ECs之间的相互作用。我们的研究旨在探索GPM6a和ICAM5在海马培养神经元和细胞系中的功能关系。体外培养15天(DIV)的神经元免疫染色显示,内源性GPM6a簇与树突干中的ICAM5簇有显著共定位。在5 DIV时,通过在N2a细胞和海马神经元中过表达GPM6a和ICAM5,进一步证实了这些结果。此外,共免疫沉淀和细胞聚集试验的结果证明了在过表达GPM6a/ICAM5的HEK293细胞中,这两种蛋白之间存在顺式和反式相互作用。此外,GPM6a和ICAM5的过表达相加增强了N2a细胞中的神经突长度、神经突数量以及5 DIV神经元中的丝状伪足形成,表明它们具有协同作用。这些发现突出了GPM6a和ICAM5在神经元发育过程中的动态关联,为它们对神经突生长、丝状伪足形成和细胞间相互作用的贡献提供了见解。

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