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紧密连接蛋白11通过干细胞因子调节免疫屏障形成和精原细胞增殖。

Claudin-11 regulates immunological barrier formation and spermatogonial proliferation through stem cell factor.

作者信息

Sugawara Taichi, Sonoda Kayoko, Chompusri Nattapran, Noguchi Kazuhiro, Okada Seiji, Furuse Mikio, Wakayama Tomohiko

机构信息

Department of Histology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Division of Hematopoiesis, Joint Research Center for Human Retrovirus Infection, Kumamoto University, Kumamoto, Japan.

出版信息

Commun Biol. 2025 Jan 30;8(1):148. doi: 10.1038/s42003-025-07592-0.

Abstract

Tight junctions (TJs) between adjacent Sertoli cells are believed to form immunological barriers that protect spermatogenic cells expressing autoantigens from autoimmune responses. However, there is no direct evidence that Sertoli cell TJs (SCTJs) do indeed form immunological barriers. Here, we analyzed male mice lacking claudin-11 (Cldn11), which encodes a SCTJ component, and found autoantibodies against antigens of spermatocytes/spermatids in their sera. Defective spermatogenesis in Cldn11-deficient mice was not restored on a recombination activating gene 2 (Rag2) knockout background lacking mature T and B lymphocytes. This suggests that adaptive immune responses to spermatogenic cells are not a cause of defective spermatogenesis in Cldn11-deficient mice. Further analyses showed that Cldn11 knockout impaired Sertoli cell polarization, localization of stem cell factor (SCF) (a key molecule for maintaining differentiating spermatogonia) to the basal compartment of seminiferous tubules, and also proliferation of differentiating spermatogonia. We propose that CLDN11 creates a microenvironment for SCF-mediated spermatogonial proliferation at the basal compartment via Sertoli cell polarization.

摘要

相邻支持细胞之间的紧密连接(TJs)被认为形成了免疫屏障,可保护表达自身抗原的生精细胞免受自身免疫反应的影响。然而,目前尚无直接证据表明支持细胞紧密连接(SCTJs)确实形成了免疫屏障。在此,我们分析了缺乏编码SCTJ成分的claudin-11(Cldn11)的雄性小鼠,发现其血清中存在针对精母细胞/精子细胞抗原的自身抗体。在缺乏成熟T和B淋巴细胞的重组激活基因2(Rag2)敲除背景下,Cldn11缺陷小鼠的生精缺陷并未得到恢复。这表明对生精细胞的适应性免疫反应不是Cldn11缺陷小鼠生精缺陷的原因。进一步分析表明,Cldn11敲除会损害支持细胞极化、干细胞因子(SCF)(维持分化型精原细胞的关键分子)在生精小管基底区的定位,以及分化型精原细胞的增殖。我们提出,CLDN11通过支持细胞极化在基底区为SCF介导的精原细胞增殖创造了一个微环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dc8/11782696/c69f77167b03/42003_2025_7592_Fig1_HTML.jpg

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