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细胞外亲环素A在牛体内具有趋化活性。

Extracellular cyclophilin A possesses chemotaxic activity in cattle.

作者信息

Takanashi Satoru, Nochi Tomonori, Abe Miku, Itaya Nanami, Urakawa Megumi, Sato Katsuyoshi, Zhuang Tao, Umemura Saori, Hayashi Tomohito, Kiku Yoshio, Kitazawa Haruki, Rose Michael T, Watanabe Kouichi, Aso Hisashi

机构信息

Laboratory of Mucosal Immunology, Graduate School of Agricultural Science, Tohoku University, Miyagi, 981-8555, Japan.

International Education and Research Center for Food and Agricultural Immunology, Graduate School of Agricultural Science, Tohoku University, Miyagi, 981-8555, Japan.

出版信息

Vet Res. 2015 Jul 11;46(1):80. doi: 10.1186/s13567-015-0212-1.

Abstract

Cyclophilin A (CyPA) was originally discovered in bovine thymocytes as a cytosolic binding protein of the immunosuppressive drug cyclosporine A. Recent studies have revealed that in mice and humans, CyPA is secreted from cells in injured or infected tissues and plays a role in recruiting inflammatory cells in those tissues. Here we found that in cattle abundant level of extracellular CyPA was observed in tissues with inflammation. To aid in investigating the role of extracellular CyPA in cattle, we generated recombinant bovine CyPA (rbCyPA) and tested its biological activity as an inflammatory mediator. When bovine peripheral blood cells were treated with rbCyPA in vitro, we observed that rbCyPA reacts with the membranous surface of granulocytes, monocytes and lymphocytes. Chemotaxis analysis showed that the granulocytes migrate toward rbCyPA and the migration is inhibited by pre-treatment with an anti-bovine CyPA antibody. These results indicate that, as for mice and humans, extracellular CyPA possesses chemotactic activity to recruit inflammatory cells (e.g., granulocytes) in cattle, and could thus be a potential therapeutic target for the treatment of inflammation.

摘要

亲环蛋白A(CyPA)最初是在牛胸腺细胞中作为免疫抑制药物环孢素A的胞质结合蛋白被发现的。最近的研究表明,在小鼠和人类中,CyPA是从受伤或感染组织中的细胞分泌出来的,并在招募这些组织中的炎症细胞方面发挥作用。在这里,我们发现,在牛身上,炎症组织中观察到细胞外CyPA水平很高。为了帮助研究细胞外CyPA在牛体内的作用,我们制备了重组牛CyPA(rbCyPA),并测试了其作为炎症介质的生物活性。当在体外使用rbCyPA处理牛外周血细胞时,我们观察到rbCyPA与粒细胞、单核细胞和淋巴细胞的膜表面发生反应。趋化性分析表明,粒细胞向rbCyPA迁移,并且这种迁移被抗牛CyPA抗体预处理所抑制。这些结果表明,对于小鼠和人类而言,细胞外CyPA具有招募牛体内炎症细胞(如粒细胞)的趋化活性,因此可能是治疗炎症的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4593/4498507/32c597efa8c8/13567_2015_212_Fig1_HTML.jpg

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