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ITGB4 缺乏通过上调 RSV 感染气道上皮细胞中的 MUC5AC 诱导黏液过度分泌。

ITGB4 deficiency induces mucus hypersecretion by upregulating MUC5AC in RSV-infected airway epithelial cells.

机构信息

Department of Physiology, School of Basic Medicine Science, Central South University, Changsha, Hunan, China.

Centre for Asthma and Respiratory Disease, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle and Hunter Medical Research Institute, Callaghan, New South Wales, Australia.

出版信息

Int J Biol Sci. 2022 Jan 1;18(1):349-359. doi: 10.7150/ijbs.66215. eCollection 2022.

Abstract

Respiratory syncytial virus (RSV) infection is the main cause of bronchiolitis in children. Excessive mucus secretion is one of the primary symbols in RSV related lower respiratory tract infections (RSV-related LRTI), which is closely associated with the occurrence and development of asthma in later life. Integrin β4 (ITGB4) is down-regulated in the airway epithelial cells (AECs) of asthma patients which plays a critical role in the pathogenesis of asthma. However, whether ITGB4 is involved in the pathological processes of RSV infection remains unclear. In this study, we found that decreased expression of ITGB4 was negatively correlated with the level of MUC5AC in childhood AECs following RSV infection. Moreover, ITGB4 deficiency led to mucus hypersecretion and MUC5AC overexpression in the small airway of RSV-infected mice. MUC5AC expression was upregulated by ITGB4 in HBE cells through EGFR, ERK and c-Jun pathways. EGFR inhibitors treatment inhibited mucus hypersecretion and MUC5AC overexpression in ITGB4-deficient mice after RSV infection. Together, these results demonstrated that epithelial ITGB4 deficiency induces mucus hypersecretion by upregulating the expression of MUC5AC through EGFR/ERK/c-Jun pathway, which further associated with RSV-related LRTI.

摘要

呼吸道合胞病毒(RSV)感染是儿童毛细支气管炎的主要病因。过度分泌黏液是 RSV 相关下呼吸道感染(RSV 相关 LRTI)的主要标志之一,与成年后哮喘的发生和发展密切相关。整合素 β4(ITGB4)在哮喘患者的气道上皮细胞(AECs)中下调,在哮喘发病机制中起关键作用。然而,ITGB4 是否参与 RSV 感染的病理过程尚不清楚。在这项研究中,我们发现 RSV 感染后,儿童 AECs 中 ITGB4 的表达降低与 MUC5AC 的水平呈负相关。此外,ITGB4 缺乏导致 RSV 感染小鼠小气道黏液过度分泌和 MUC5AC 过度表达。ITGB4 通过 EGFR、ERK 和 c-Jun 途径在上皮细胞 HBE 中上调 MUC5AC 的表达。EGFR 抑制剂治疗抑制 RSV 感染后 ITGB4 缺陷型小鼠的黏液过度分泌和 MUC5AC 过度表达。综上所述,这些结果表明上皮细胞 ITGB4 缺乏通过 EGFR/ERK/c-Jun 途径上调 MUC5AC 的表达诱导黏液过度分泌,进一步与 RSV 相关 LRTI 相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c28c/8692133/17c658731af1/ijbsv18p0349g001.jpg

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