Suppr超能文献

四跨膜蛋白CD53通过稳定L-选择素的表面表达促进淋巴细胞再循环。

Tetraspanin CD53 Promotes Lymphocyte Recirculation by Stabilizing L-Selectin Surface Expression.

作者信息

Demaria Maria C, Yeung Louisa, Peeters Rens, Wee Janet L, Mihaljcic Masa, Jones Eleanor L, Nasa Zeyad, Alderuccio Frank, Hall Pamela, Smith Brodie C, Binger Katrina J, Hammerling Gunther, Kwok Hang Fai, Newman Andrew, Ager Ann, van Spriel Annemiek, Hickey Michael J, Wright Mark D

机构信息

Department of Immunology and Pathology, Monash University, Alfred Research Alliance, Melbourne, VIC 3004, Australia.

Department of Immunology and Pathology, Monash University, Alfred Research Alliance, Melbourne, VIC 3004, Australia; Centre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, 246 Clayton Road, Clayton, VIC 3168, Australia.

出版信息

iScience. 2020 May 22;23(5):101104. doi: 10.1016/j.isci.2020.101104. Epub 2020 Apr 27.

Abstract

Tetraspanins regulate key processes in immune cells; however, the function of the leukocyte-restricted tetraspanin CD53 is unknown. Here we show that CD53 is essential for lymphocyte recirculation. Lymph nodes of Cd53 mice were smaller than those of wild-type mice due to a marked reduction in B cells and a 50% decrease in T cells. This reduced cellularity reflected an inability of Cd53 B and T cells to efficiently home to lymph nodes, due to the near absence of L-selectin from Cd53 B cells and reduced stability of L-selectin on Cd53 T cells. Further analyses, including on human lymphocytes, showed that CD53 stabilizes L-selectin surface expression and may restrain L-selectin shedding via both ADAM17-dependent and ADAM17-independent mechanisms. The disruption in lymphocyte recirculation in Cd53 mice led to impaired immune responses dependent on antigen delivery to lymph nodes. Together these findings demonstrate an essential role for CD53 in lymphocyte trafficking and immunity.

摘要

四跨膜蛋白调节免疫细胞中的关键过程;然而,白细胞限制性四跨膜蛋白CD53的功能尚不清楚。在此我们表明,CD53对淋巴细胞再循环至关重要。Cd53基因敲除小鼠的淋巴结比野生型小鼠的小,这是由于B细胞显著减少以及T细胞减少50%。这种细胞数量减少反映出Cd53基因敲除的B细胞和T细胞无法有效地归巢至淋巴结,这是因为Cd53基因敲除的B细胞几乎不存在L-选择素,且Cd53基因敲除的T细胞上L-选择素的稳定性降低。包括对人类淋巴细胞的进一步分析表明,CD53可稳定L-选择素的表面表达,并可能通过依赖ADAM17和不依赖ADAM17的机制抑制L-选择素的脱落。Cd53基因敲除小鼠中淋巴细胞再循环的破坏导致依赖于抗原递送至淋巴结的免疫反应受损。这些发现共同证明了CD53在淋巴细胞运输和免疫中的重要作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验