Influenza virus reduces ubiquitin E3 ligase MARCH10 expression to decrease ciliary beat frequency

Author:

Tsai MuChun1ORCID,Rayner Rachael E.2ORCID,Chafin Lexie1,Farkas Daniela1ORCID,Adair Jessica1,Mishan Chelsea1,Mallampalli Rama K.1ORCID,Kim Sun Hee2,Cormet-Boyaka Estelle2ORCID,Londino James D.1ORCID

Affiliation:

1. Division of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, The Ohio State University, Columbus, Ohio, United States

2. Department of Veterinary Biosciences, The Ohio State University, Columbus, Ohio, United States

Abstract

Respiratory viruses, such as influenza, decrease airway cilia function and expression, which leads to reduced mucociliary clearance and inhibited overall immune defense. Ubiquitination is a posttranslational modification using E3 ligases, which plays a role in the assembly and disassembly of cilia. We examined the role of membrane-associated RING-CH (MARCH) family of E3 ligases during influenza infection and determined that MARCH10, specifically expressed in ciliated epithelial cells, is significantly decreased during influenza infection in mice, human lung epithelial cells, and human lung tissue. Cellular depletion of MARCH10 in differentiated human bronchial epithelial cells (HBECs) using CRISPR/Cas9 showed a decrease in ciliary beat frequency. Furthermore, MARCH10 cellular knockdown in combination with influenza infection selectively decreased immunoreactive levels of the ciliary component, dynein axonemal intermediate chain 1. Cellular overexpression of MARCH10 significantly decreased influenza hemagglutinin protein levels in the differentiated HBECs and knockdown of MARCH10 increased IL-1β cytokine expression, whereas overexpression had the reciprocal effect. These findings suggest that MARCH10 may have a protective role in airway pulmonary host defense and innate immunity during influenza infection.

Funder

John Templeton Foundation

Cystic Fibrosis Foundation

Doris Duke Charitable Foundation

HHS | NIH | National Heart, Lung, and Blood Institute

OSU | College of Medicine Office of Research, Ohio State University

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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