Dynasore inhibits removal of wild-type and ΔF508 cystic fibrosis transmembrane conductance regulator (CFTR) from the plasma membrane

Author:

Young Andrew1,Gentzsch Martina2,Abban Cynthia Y.3,Jia Ying1,Meneses Patricio I.3,Bridges Robert J.1,Bradbury Neil A.1

Affiliation:

1. Department of Physiology and Biophysics, Chicago Medical School, 3333 Green Bay Road, North Chicago, IL 60064, U.S.A.

2. Cell and Developmental Biology, UNC Chapel Hill, 6109A Thurston-Bowles CB# 7248, Chapel Hill, NC 27599, U.S.A.

3. Department of Microbiology and Immunology, Chicago Medical School, 3333 Green Bay Road, North Chicago, IL 60064, U.S.A.

Abstract

Dynasore, a small molecule inhibitor of dynamin, was used to probe the role of dynamin in the endocytosis of wild-type and mutant CFTR (cystic fibrosis transmembrane conductance regulator). Internalization of both wild-type and ‘temperature-corrected’ ΔF508 CFTR was markedly inhibited by a short exposure to dynasore, implicating dynamin as a key element in the endocytic internalization of both wild-type and mutant CFTR. The inhibitory effect of dynasore was readily reversible upon washout of dynasore from the growth media. Corr-4 ({2-(5-chloro-2-methoxy-phenylamino)-4′-methyl-[4,5′]-bithiazolyl-2′-yl}-phenyl-methanonone), a pharmacological corrector of ΔF508 CFTR biosynthesis, caused a marked increase in the cell surface expression of mutant CFTR. Co-incubation of ΔF508 CFTR expressing cells with Corr-4 and dynasore caused a significantly greater level of cell surface CFTR than that observed in the presence of Corr-4 alone. These results argue that inhibiting the endocytic internalization of mutant CFTR provides a novel therapeutic target for augmenting the benefits of small molecule correctors of mutant CFTR biosynthesis.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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