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DOI 10.1016/j.imlet.2016.11.016

Медицинская библиотека · Immunology letters · 2016

Anti-CD24 neutralizing antibody exacerbates Concanavalin A-induced acute liver injury in mice via liver M1 macrophages.

Liu Hongyu, Hai Lei, Tian Jingqi, Xiang Jie, Fan Yatong, Zhang Hua, Liu Jianhui, Zhang Xuejun

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Liver largely relies on its innate immunity to initiate quick and effective defense against potentially toxic agents, and innate immune cells are major players in this process. However, excessive inflammation due to out-of-control immune response may eventually cause liver injury. Thus, it is important to fully understand the regulatory mechanisms associated with liver inflammation. Here we showed that anti-CD24 neutralizing antibody exacerbated hepatic inflammation in a Con A-induced acute liver injury murine model. Our results supported that hepatic macrophages were required for anti-CD24 neutralizing antibody-aggravated liver inflammation, as depletion of macrophages significantly alleviated Con A-induced inflammation. M1 macrophages, but not M2 macrophages, were specifically induced by Con A, and more greatly by Con A in combination with anti-CD24 neutralizing antibody. The combined treatment further promoted M1 hepatic macrophages to express TNF-α, which increased hepatocytes apoptosis. Taken together, these data suggest that anti-CD24 neutralizing antibody plays an important role in aggravating inflammation in the process of Con A-induced acute liver injury in mice. The possible mechanism might involve the enhanced secretion of TNF-α by hepatic M1 macrophages. This study also implicates a role for CD24 in negative regulation of Con A-induced liver inflammation.

Для цитирования: Liu Hongyu, Hai Lei, Tian Jingqi, Xiang Jie, Fan Yatong, Zhang Hua, Liu Jianhui, Zhang Xuejun. Anti-CD24 neutralizing antibody exacerbates Concanavalin A-induced acute liver injury in mice via liver M1 macrophages.. Immunology letters. 2016. DOI: 10.1016/j.imlet.2016.11.016.

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