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Here we show that caveolin-1-deficient fibroblasts lacking caveolae upregulate a tubular endocytic pathway, and have a reduced capacity to reseal after permeabilization with pore-forming toxins when compared to wild type cells. Silencing endophilin-A2 expression inhibited fission of endocytic tubules and further reduced plasma membrane repair in cells lacking caveolin-1, supporting a role for tubular endocytosis as an alternative pathway for the removal of membrane lesions. Endophilin-A2 was visualized in association with cholera toxin B-containing endosomes and was recruited to recently formed intracellular vacuoles containing Trypanosoma cruzi, a parasite that utilizes the plasma membrane wounding\/repair pathway to invade host cells. Endophilin-A2 deficiency inhibited T. cruzi invasion, and fibroblasts deficient in both caveolin-1 and endophilin-A2 did not survive prolonged exposure to the parasites. These findings reveal a novel cross-talk between caveolin-1 and endophilin-A2 in the regulation of clathrin-independent endocytosis and plasma membrane repair, a process that is subverted by T. cruzi parasites for cell invasion.<\/jats:p>","DOI":"10.1242\/jcs.249524","type":"journal-article","created":{"date-parts":[[2020,10,22]],"date-time":"2020-10-22T18:30:11Z","timestamp":1603391411000},"source":"Crossref","is-referenced-by-count":15,"title":["Endophilin-A2 dependent tubular endocytosis promotes plasma membrane repair and parasite invasion"],"prefix":"10.1242","author":[{"given":"Matthias","family":"Corrotte","sequence":"first","affiliation":[{"name":"Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742 USA"},{"name":"Department of Veterinary Medicine, VA-MD College of Veterinary Medicine, University of Maryland, College Park, MD, 20742 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mark","family":"Cerasoli","sequence":"additional","affiliation":[{"name":"Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fernando Y.","family":"Maeda","sequence":"additional","affiliation":[{"name":"Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0611-2412","authenticated-orcid":false,"given":"Norma W.","family":"Andrews","sequence":"additional","affiliation":[{"name":"Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[2020,1,1]]},"reference":[{"key":"2021042623324537400_JCS249524C1","doi-asserted-by":"publisher","first-page":"6982","DOI":"10.1073\/pnas.1402233111","article-title":"Endophilin A1 induces different membrane shapes using a conformational switch that is regulated by phosphorylation","volume":"111","author":"Ambroso","year":"2014","journal-title":"Proc. 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