Loss of lipid asymmetry facilitates plasma membrane blebbing by decreasing membrane lipid packing
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
Journal Info
Proceedings of the National Academy of Sciences
National Academy of Sciences
Authors (8)
Hong-Yin Wang
Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia
Alissa Rumin
Molecular and Cellular Biophysics Program, Department of Biological Sciences, University of Denver
Milka Doktorova
Department of Molecular Physiology and Biological Physics, University of Virginia
Daryna Sputay
Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia
Sze Ham Chan
Department of Molecular Physiology and Biological Physics, Center for Membrane and Cell Physiology, University of Virginia
Ann M. Wehman
Kandice R. Levental
Department of Molecular Physiology and Biological Physics, University of Virginia
Ilya Levental
Department of Molecular Physiology and Biological Physics, University of Virginia