دورية أكاديمية

Roles of Sialic Acid, AXL, and MER Receptor Tyrosine Kinases in Mumps Virus Infection of Mouse Sertoli and Leydig Cells

التفاصيل البيبلوغرافية
العنوان: Roles of Sialic Acid, AXL, and MER Receptor Tyrosine Kinases in Mumps Virus Infection of Mouse Sertoli and Leydig Cells
المؤلفون: Fei Wang, Ran Chen, Qian Jiang, Han Wu, Maolei Gong, Weihua Liu, Xiaoqin Yu, Wenjing Zhang, Ruiqin Han, Aijie Liu, Yongmei Chen, Daishu Han
المصدر: Frontiers in Microbiology, Vol 11 (2020)
بيانات النشر: Frontiers Media S.A., 2020.
سنة النشر: 2020
المجموعة: LCC:Microbiology
مصطلحات موضوعية: mumps virus, testis, sialic acid, AXL, MER, Microbiology, QR1-502
الوصف: The mumps virus (MuV) causes epidemic parotitis. MuV also frequently infects the testis and induces orchitis, an important etiological factor contributing to male infertility. However, mechanisms underlying MuV infection of the testis remain unknown. Here, we describe that sialic acid, AXL, and MER receptor tyrosine kinases regulate MuV entry and replication in mouse major testicular cells, including Sertoli and Leydig cells. Sialic acid, AXL, and MER were present in Sertoli and Leydig cells. Sialic acid specifically mediated MuV entry into Sertoli and Leydig cells, whereas both AXL and MER facilitated MuV replication within cells through the inhibition of cellular innate antiviral responses. Mechanistically, the inhibition of type 1 interferon signaling by AXL and MER is essential for MuV replication in Sertoli and Leydig cells. Our findings provide novel insights into the mechanisms behind MuV infection and replication in the testis.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1664-302X
العلاقة: https://www.frontiersin.org/article/10.3389/fmicb.2020.01292/fullTest; https://doaj.org/toc/1664-302XTest
DOI: 10.3389/fmicb.2020.01292
الوصول الحر: https://doaj.org/article/a2c25529d84f4e4a8d9fca8d7106e865Test
رقم الانضمام: edsdoj.2c25529d84f4e4a8d9fca8d7106e865
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1664302X
DOI:10.3389/fmicb.2020.01292