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人自然杀伤细胞抗体依赖的细胞介导的细胞毒性溶解突触中CD16a的空间定位。

Spatial localization of CD16a at the human NK cell ADCC lytic synapse.

作者信息

Ross Patrick, Fatima Hijab, Leaman Dan P, Matthias Jessica, Spencer Kathryn, Zwick Michael B, Henderson Scott C, Mace Emily M, Murin Charles Daniel

机构信息

San Diego Biomedical Research Institute, San Diego, CA, USA.

Department of Integrative Structural and Computational Biology, Scripps Research, La Jolla, CA, USA.

出版信息

bioRxiv. 2024 Aug 10:2024.08.09.605851. doi: 10.1101/2024.08.09.605851.

Abstract

Natural Killer (NK) cells utilize effector functions, including antibody-dependent cellular cytotoxicity (ADCC), for the clearance of viral infection and cellular malignancies. NK cell ADCC is mediated by FcRIIIa (CD16a) binding to the fragment crystallizable (Fc) region of immunoglobulin G (IgG) within immune complexes on a target cell surface. While antibody-induced clustering of CD16a is thought to drive ADCC, the molecular basis for this activity has not been fully described. Here we use MINFLUX nanoscopy to map the spatial distribution of stoichiometrically labeled CD16a across the NK cell membrane, revealing the presence of pairs of CD16a molecules with intra-doublet distance of approximately 17 nm. NK cells activated on supported lipid bilayers by Trastuzumab results in an increase of synaptic regions with greater CD16a density. Our results provide the highest spatial resolution yet described for CD16a imaging, offering new insight into how CD16a organization within the immune synapse could influence ADCC activity. MINFLUX holds great promise to further unravel the molecular details driving CD16a-based activation of NK cells.

摘要

自然杀伤(NK)细胞利用包括抗体依赖性细胞毒性(ADCC)在内的效应功能来清除病毒感染和细胞恶性肿瘤。NK细胞ADCC由FcRIIIa(CD16a)与靶细胞表面免疫复合物中免疫球蛋白G(IgG)的可结晶片段(Fc)区域结合介导。虽然认为抗体诱导的CD16a聚集驱动ADCC,但这种活性的分子基础尚未完全阐明。在这里,我们使用MINFLUX纳米显微镜来绘制化学计量标记的CD16a在NK细胞膜上的空间分布,揭示了成对的CD16a分子的存在,其双联体内部距离约为17nm。曲妥珠单抗在支持的脂质双层上激活NK细胞会导致具有更高CD16a密度的突触区域增加。我们的结果提供了迄今为止描述的CD16a成像的最高空间分辨率,为免疫突触内CD16a的组织如何影响ADCC活性提供了新的见解。MINFLUX有望进一步揭示驱动基于CD16a的NK细胞激活的分子细节。

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