Apical size reduction by macropinocytosis alleviates tissue crowding

E Enzo Bresteau E Eve E. Suva C Christopher Revell O Osama A. Hassan A Aline Grata J Jennifer Sheridan J Jennifer Mitchell C Constadina Arvanitis (Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine) F Farida Korobova S Sarah Woolner O Oliver E. Jensen B Brian Mitchell

Abstract

Abstract Tissue crowding represents a critical challenge to epithelial tissues, which often respond via the irreversible process of live cell extrusion. We report that apical size reduction via macropinocytosis serves as a malleable and less destructive form of tissue remodeling that can alleviate the need for cell loss. We find that macropinocytosis is triggered by tissue crowding via mechanosensory signaling, leading to substantial internalization of apical membrane. This drives a reduction in apical surface which alleviates crowding. We report that this mechanism regulates the long-term organization of the developing epithelium and controls the timing of proliferation-induced cell extrusion. Additionally, we observe a wave of macropinocytosis in response to acute external compression. In both scenarios, inhibiting macropinocytosis induces a dramatic increase in cell extrusion suggesting cooperation between cell extrusion and macropinocytosis in response to both developmental and external compression. Our findings implicate macropinocytosis as an important regulator of dynamic epithelial remodeling.

Article Details

Volume / Issue Vol. 16, Issue 1
Published June 23, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (12)

E

Enzo Bresteau

E

Eve E. Suva

C

Christopher Revell

O

Osama A. Hassan

A

Aline Grata

J

Jennifer Sheridan

J

Jennifer Mitchell

C

Constadina Arvanitis

Department of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine

F

Farida Korobova

S

Sarah Woolner

O

Oliver E. Jensen

B

Brian Mitchell