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敲低和敲除模型揭示的Tspan8和CD151的联合特征及互补性。

Joint features and complementarities of Tspan8 and CD151 revealed in knockdown and knockout models.

作者信息

Yue Shijing, Zhao Kun, Erb Ulrike, Rana Sanyukta, Zöller Margot

机构信息

Tumor Cell Biology, University Hospital of Surgery, Im Neuenheimer Feld 365, Heidelberg D 69120, Germany.

School of Medicine, Nankai University, Tianjin, China.

出版信息

Biochem Soc Trans. 2017 Apr 15;45(2):437-447. doi: 10.1042/BST20160298.

Abstract

Tetraspanins are highly conserved 4-transmembrane proteins which form molecular clusters with a large variety of transmembrane and cytosolic proteins. By these associations tetraspanins are engaged in a multitude of biological processes. Furthermore, tetraspanin complexes are located in specialized microdomains, called tetraspanin-enriched microdomains (TEMs). TEMs provide a signaling platform and are poised for invagination and vesicle formation. These vesicles can be released as exosomes (Exo) and are important in cell contact-independent intercellular communication. Here, we summarize emphasizing knockdown and knockout models' pathophysiological joint and selective activities of CD151 and Tspan8, and discuss the TEM-related engagement of CD151 and Tspan8 in Exo activities.

摘要

四跨膜蛋白是高度保守的四跨膜蛋白,它们与多种跨膜蛋白和胞质蛋白形成分子簇。通过这些关联,四跨膜蛋白参与了众多生物学过程。此外,四跨膜蛋白复合物位于称为富含四跨膜蛋白微区(TEMs)的特殊微区中。TEMs提供了一个信号平台,易于内陷和囊泡形成。这些囊泡可以作为外泌体(Exo)释放,并且在细胞非接触依赖性细胞间通讯中很重要。在这里,我们着重总结了敲低和敲除模型中CD151和Tspan8的病理生理联合和选择性活性,并讨论了CD151和Tspan8在TEM相关的外泌体活性中的作用。

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