Abstract

SummaryCaveolae introduce flask-shaped convolutions into the plasma membrane and help to protect the plasma membrane from damage under stretch forces. The protein components that form the bulb of caveolae are increasingly well characterized, but less is known about the contribution of proteins that localize to the constricted neck. Here we make extensive use of multiple CRISPR/Cas9-generated gene knockout and knockin cell lines to investigate the role of Eps15 Homology Domain (EHD) proteins at the neck of caveolae. We show that EHD1, EHD2, and EHD4 are recruited to caveolae. Recruitment of the other EHDs increases markedly when EHD2, which has been previously detected at caveolae, is absent. Construction of knockout cell lines lacking EHDs 1, 2, and 4 confirms this apparent functional redundancy. Two striking sets of phenotypes are observed in EHD1,2,4 knockout cells: (1) the characteristic clustering of caveolae into higher-order assemblies is absent; and (2) when the EHD1,2,4 knockout cells are subjected to prolonged cycles of stretch forces, caveolae are destabilized and the plasma membrane is prone to rupture. Our data identify the first molecular components that act to cluster caveolae into a membrane ultrastructure with the potential to extend stretch-buffering capacity and support a revised model for the function of EHDs at the caveolar neck.

Highlights

  • Caveolae are flask-shaped invaginations of the plasma membrane

  • In order to assay dynamics of caveolae in DEHD2 cells, CRISPR/Cas9 and an appropriate targeting construct were used to express GFP fused to the C terminus of endogenous caveolin1

  • Fluorescence recovery after photobleaching (FRAP) experiments on these cells, and control NIH 3T3 cells where endogenous caveolin1 had been tagged in the same way [30], did not detect altered mobility of caveolin1-GFP in the DEHD2 cells (Figure S1C)

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Summary

Introduction

Caveolae are flask-shaped invaginations of the plasma membrane. They are especially abundant in endothelial cells, adipocytes, and muscle cells [1, 2]. Caveolae protect cells from rupture of the plasma membrane under mechanical stress [3, 4]. Further activities of caveolae in sensing mechanical force and transducing consequent intracellular signals are likely to be significant [3, 8], and caveolae may help maintain membrane integrity through endocytosis of damaged membrane regions [9, 10]. Caveolae have been associated with a range of additional functions, including signal transduction, lipid homeostasis, and endocytosis [8, 11,12,13,14,15,16,17]

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