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超分辨率成像揭示CD81微结构域在调节Jurkat T细胞微绒毛膜信号传导中的空间组织。

Superresolution Imaging Reveals the Spatial Organization of CD81 Microdomains in Regulating Membrane Signaling on Jurkat T Cell Microvilli.

作者信息

Ramseier Neal T, Jing Haoran, Anderson Jesse, Hu Ying S

机构信息

Department of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, IL 60607, USA.

Department of Chemical Engineering, College of Engineering, University of Illinois Chicago, Chicago, IL 60607, USA.

出版信息

bioRxiv. 2024 Dec 12:2024.12.07.627345. doi: 10.1101/2024.12.07.627345.

Abstract

Tetraspanin proteins are closely associated with high-curvature membrane structures and play key roles in organizing membrane domains and regulating membrane signaling in immune cells. However, their specific roles in regulating T cell membrane signaling, particularly within the microvilli often characteristic of these cells, remain poorly understood. Here, we used Jurkat T cells as a model system and investigated CD81 as a member of the tetraspanin family. Using total internal reflection fluorescence (TIRF) microscopy and structured illumination microscopy (SIM), we identified an enrichment of the tetraspanin CD81 microdomains along the actin-rich membrane microvilli. At the distal end of the microvilli, SIM images revealed the spatial colocalization of CD81 with T cell receptors (TCR) and CD63, implying a potential role for CD81 in regulating TCR signaling in conjunction with CD63. Spatial analysis of CD81 and CD63 microdomains from the dual-color SIM data revealed their preference for associating with each other. Cluster analysis of direct stochastic optical reconstruction microscopy (STORM) data revealed that T cell activation results in reduced domain sizes and increased domain separation of CD81. These findings provide visual evidence of the spatial organization and rearrangement of CD81 on the T cell microvilli, highlighting its potential role in signal regulation on specialized membrane protrusions.

摘要

四跨膜蛋白与高曲率膜结构密切相关,在免疫细胞中组织膜结构域和调节膜信号传导方面发挥关键作用。然而,它们在调节T细胞膜信号传导中的具体作用,尤其是在这些细胞通常具有的微绒毛内的作用,仍知之甚少。在这里,我们以Jurkat T细胞为模型系统,研究了作为四跨膜蛋白家族成员的CD81。使用全内反射荧光(TIRF)显微镜和结构光照明显微镜(SIM),我们发现富含肌动蛋白的膜微绒毛上四跨膜蛋白CD81微结构域富集。在微绒毛的远端,SIM图像显示CD81与T细胞受体(TCR)和CD63在空间上共定位,这意味着CD81可能与CD63一起在调节TCR信号传导中发挥作用。对双色SIM数据中CD81和CD63微结构域的空间分析表明它们倾向于相互结合。直接随机光学重建显微镜(STORM)数据的聚类分析表明,T细胞活化导致CD81的结构域尺寸减小和结构域分离增加。这些发现为CD81在T细胞微绒毛上的空间组织和重排提供了直观证据,突出了其在特殊膜突起上信号调节中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5835/11643289/8b83d59d9770/nihpp-2024.12.07.627345v2-f0001.jpg

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