Loss of lipid asymmetry facilitates plasma membrane blebbing by decreasing membrane lipid packing

H Hong-Yin Wang (Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia) A Alissa Rumin (Molecular and Cellular Biophysics Program, Department of Biological Sciences, University of Denver) M Milka Doktorova (Department of Molecular Physiology and Biological Physics, University of Virginia) D Daryna Sputay (Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia) S Sze Ham Chan (Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia) A Ann M. Wehman K Kandice R. Levental (Department of Molecular Physiology and Biological Physics, University of Virginia) I Ilya Levental (Department of Molecular Physiology and Biological Physics, University of Virginia)

Abstract

Membrane blebs have important roles in cell migration, apoptosis, and intercellular communication through extracellular vesicles (EVs). While plasma membranes (PM) typically maintain phosphatidylserine (PS) on their cytoplasmic leaflet, most blebs have PS exposed on their outer leaflet, revealing that loss of steady-state lipid asymmetry often accompanies PM blebbing. How these changes in PM lipid organization regulate membrane properties and affect bleb formation remains unknown. We confirmed that lipid scrambling through the scramblase TMEM16F is essential for chemically induced membrane blebbing across cell types, with the kinetics of PS exposure being tightly coupled to the kinetics of bleb formation. Measurement of lipid packing with environment-sensitive probes revealed that lipid scrambling changes the physical properties of the PM, reducing lipid packing and facilitating the bilayer bending required for bleb formation. Accordingly, reducing lipid packing of the PM through cholesterol extraction, elevated temperature, or treatment with biological amphiphiles promoted blebbing in the absence of TMEM16F. Consistent with these cellular observations, blebbing in Caenorhabditis elegans embryos measured via EV production was significantly reduced by depleting the TMEM16-homolog ANOH-2. Our findings suggest that changing membrane biophysical properties by lipid scrambling is an important contributor to the formation of blebs and EVs and potentially other cellular processes involving PM deformation.

Article Details

Volume / Issue Vol. 122, Issue 19
Published May 13, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (8)

H

Hong-Yin Wang

Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia

A

Alissa Rumin

Molecular and Cellular Biophysics Program, Department of Biological Sciences, University of Denver

M

Milka Doktorova

Department of Molecular Physiology and Biological Physics, University of Virginia

D

Daryna Sputay

Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia

S

Sze Ham Chan

Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia

A

Ann M. Wehman

K

Kandice R. Levental

Department of Molecular Physiology and Biological Physics, University of Virginia

I

Ilya Levental

Department of Molecular Physiology and Biological Physics, University of Virginia