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Krüppel 样因子 2 控制 IgA 浆细胞区室化和 IgA 应答。

Krüppel-like factor 2 controls IgA plasma cell compartmentalization and IgA responses.

机构信息

Division of Molecular Immunology, Department of Internal Medicine 3, Nikolaus-Fiebiger Center, University Hospital Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany.

Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.

出版信息

Mucosal Immunol. 2022 Apr;15(4):668-682. doi: 10.1038/s41385-022-00503-0. Epub 2022 Mar 28.

Abstract

Krüppel-like factor 2 (KLF2) is a potent regulator of lymphocyte differentiation, activation and migration. However, its functional role in adaptive and humoral immunity remains elusive. Therefore, by using mice with a B cell-specific deletion of KLF2, we investigated plasma cell differentiation and antibody responses. We revealed that the deletion of KLF2 resulted in perturbed IgA plasma cell compartmentalization, characterized by the absence of IgA plasma cells in the bone marrow, their reductions in the spleen, the blood and the lamina propria of the colon and the small intestine, concomitant with their accumulation and retention in mesenteric lymph nodes and Peyer's patches. Most intriguingly, secretory IgA in the intestinal lumen was almost absent, dimeric serum IgA was drastically reduced and antigen-specific IgA responses to soluble Salmonella flagellin were blunted in KLF2-deficient mice. Perturbance of IgA plasma cell localization was caused by deregulation of CCR9, Integrin chains αM, α4, β7, and sphingosine-1-phosphate receptors. Hence, KLF2 not only orchestrates the localization of IgA plasma cells by fine-tuning chemokine receptors and adhesion molecules but also controls IgA responses to Salmonella flagellin.

摘要

Krüppel 样因子 2(KLF2)是淋巴细胞分化、激活和迁移的有效调节剂。然而,其在适应性和体液免疫中的功能作用仍不清楚。因此,我们利用 B 细胞特异性敲除 KLF2 的小鼠,研究浆细胞分化和抗体反应。结果表明,KLF2 的缺失导致 IgA 浆细胞区室化受到干扰,特征为骨髓中缺乏 IgA 浆细胞,脾脏、血液和结肠及小肠固有层中的 IgA 浆细胞减少,同时在肠系膜淋巴结和派尔集合淋巴结中积累和保留。最有趣的是,肠道腔中的分泌型 IgA 几乎不存在,二聚体血清 IgA 明显减少,对可溶性沙门氏菌鞭毛蛋白的抗原特异性 IgA 反应减弱。IgA 浆细胞定位的紊乱是由 CCR9、整合素链 αM、α4、β7 和鞘氨醇-1-磷酸受体的失调引起的。因此,KLF2 不仅通过微调趋化因子受体和黏附分子来协调 IgA 浆细胞的定位,而且还控制对沙门氏菌鞭毛蛋白的 IgA 反应。

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