CNR, Institute of Neuroscience, Milan 20129, Italy; BioMETRA, Department of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy; UK Dementia Research Institute at University College London, London WC1E 6BT, UK.
CNR, Institute of Neuroscience, Milan 20129, Italy; DiSFeB, Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.
Cell Rep. 2019 Oct 29;29(5):1130-1146.e8. doi: 10.1016/j.celrep.2019.09.051.
Tetraspanins are a class of evolutionarily conserved transmembrane proteins with 33 members identified in mammals that have the ability to organize specific membrane domains, named tetraspanin-enriched microdomains (TEMs). Despite the relative abundance of different tetraspanins in the CNS, few studies have explored their role at synapses. Here, we investigate the function of TSPAN5, a member of the tetraspanin superfamily for which mRNA transcripts are found at high levels in the mouse brain. We demonstrate that TSPAN5 is localized in dendritic spines of pyramidal excitatory neurons and that TSPAN5 knockdown induces a dramatic decrease in spine number because of defects in the spine maturation process. Moreover, we show that TSPAN5 interacts with the postsynaptic adhesion molecule neuroligin-1, promoting its correct surface clustering. We propose that membrane compartmentalization by tetraspanins represents an additional mechanism for regulating excitatory synapses.
四跨膜蛋白是一类进化上保守的跨膜蛋白,在哺乳动物中已鉴定出 33 个成员,它们具有组织特定膜域的能力,这些膜域被命名为四跨膜蛋白富集微域(TEMs)。尽管中枢神经系统中不同四跨膜蛋白的相对丰度不同,但很少有研究探索它们在突触中的作用。在这里,我们研究了四跨膜蛋白超家族成员 TSPAN5 的功能,该蛋白的 mRNA 转录本在小鼠大脑中高水平表达。我们证明 TSPAN5 定位于锥体兴奋性神经元的树突棘中,并且 TSPAN5 敲低会导致由于棘突成熟过程中的缺陷而导致棘突数量的急剧减少。此外,我们表明 TSPAN5 与突触后粘附分子 neuroligin-1 相互作用,促进其正确的表面聚类。我们提出,四跨膜蛋白的膜区室化代表了调节兴奋性突触的另一种机制。