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DOI 10.1016/j.ajpath.2020.02.004

Медицинская библиотека · The American journal of pathology · 2020

Sympathetic Nerves Positively Regulate Eosinophil-Driven Allergic Conjunctivitis via α1-Adrenergic Receptor Signaling.

Liu Jun, Huang Shuoya, Li Fanying, Wu Mingjuan, He Jingxin, Xue Yunxia, Fu Ting, Yu Ruoxun, Chen Xinwei, Wang Yuming, Li Zhijie

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Eosinophils are a major cause of tissue injury in allergic conjunctivitis. The biological nature of eosinophils in the conjunctiva and the mechanisms that control eosinophils' responses in allergic conjunctivitis are currently not completely understood. This study reports that conjunctival eosinophils comprise two populations-Siglec-Fint and Siglec-Fhi-in different life stages. Siglec-Fint eosinophils partly expressed CD34 and were in the immature (or steady) state. Siglec-Fhi eosinophils did not express CD34, sharply increased in number after short ragweed (SRW) pollen challenge, and were in the mature (or activated) state. Moreover, chemical sympathectomy by 6-hydroxydopamine reduced the recruitment and activation of eosinophils, whereas the activation of the sympathetic nerve system (SNS) with restraint stress accelerated the recruitment and activation of eosinophils in SRW-induced conjunctivitis. It was also found that two eosinophil populations expressed alpha-1a-adrenergic receptors (α1a-ARs); in SRW-induced conjunctivitis, treatment with an α1a-AR antagonist decreased eosinophil responses, whereas treatment with an α1a-AR agonist aggravated eosinophil responses. Thus, eosinophil responses in conjunctivitis are regulated by the SNS via α1a-AR signaling. SNS inputs or α1a-AR function may be potential targets for the treatment of allergic conjunctivitis.

Для цитирования: Liu Jun, Huang Shuoya, Li Fanying, Wu Mingjuan, He Jingxin, Xue Yunxia, Fu Ting, Yu Ruoxun, Chen Xinwei, Wang Yuming, Li Zhijie. Sympathetic Nerves Positively Regulate Eosinophil-Driven Allergic Conjunctivitis via α1-Adrenergic Receptor Signaling.. The American journal of pathology. 2020. DOI: 10.1016/j.ajpath.2020.02.004.

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