Cell fusion after wounding requires plasma membrane damage and endocytosis

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Authors: Junmin Hua, Evan S. Krystofiak, Andrew D. Pumford, Andrea Page-McCaw, M. Shane Hutson
Cited by: 1
References: 83

Abstract

pupal notum, wound-adjacent epithelial cells with plasma membrane damage often fuse to form syncytia; when plasma membrane damage is prevented, syncytia do not form. Damaged cells share cytoplasm as soon as milliseconds after wounding, and fusion pores connecting cell membranes form minutes later. A genetic screen reveals that wound-induced fusion requires endocytosis machinery, and dynamin localization indicates that endocytosis preferentially targets plasma membrane removed during fusion. Endocytosis promotes cell fusion by specifically promoting fusion pore expansion, indicated by quantitative analysis of cytoplasmic sharing between cells over time. Without endocytosis-mediated cell fusion, wound healing is slowed. Together, our results support a model of damage-induced cell fusion in which plasma membrane damage initiates fusion pores and endocytosis expands fusion pores, resulting in cellular fusion as an integration of single cell damage with tissue repair.

Fields of Study & Subjects

Cellular transport and secretion Invertebrate Immune Response Mechanisms Hippo pathway signaling and YAP/TAZ

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
2 June 2026
Language
EN
Document type
Preprint