Caveolin-1 dolines form a distinct and rapid caveolae-independent mechanoadaptation system

Fidel‐Nicolás Lolo(Spanish National Centre for Cardiovascular Research), Nikhil Walani(FC Barcelona), Eric Seemann(Jena University Hospital), Dobryna Zalvidea(Institute for Bioengineering of Catalonia), Dácil M. Pavón(Spanish National Centre for Cardiovascular Research), Gheorghe Cojoc(Technische Universität Dresden), Moreno Zamai(Spanish National Centre for Cardiovascular Research), Christine Viaris de Lesegno(Centre National de la Recherche Scientifique), Fernando Martínez(Spanish National Centre for Cardiovascular Research), Miguel Sánchez‐Álvarez(Spanish National Centre for Cardiovascular Research), Juan J. Uriarte(Universitat de Barcelona), Asier Echarri(Spanish National Centre for Cardiovascular Research), Daniel Jiménez‐Carretero(Spanish National Centre for Cardiovascular Research), Joan-Carles Escolano(Max Planck Institute for the Science of Light), Susana A. Sánchez(University of Concepción), Valeria R. Caiolfa(Spanish National Centre for Cardiovascular Research), Daniel Navajas(Institute for Bioengineering of Catalonia), Xavier Trepat(Institució Catalana de Recerca i Estudis Avançats), Jochen Guck(Max Planck Institute for the Science of Light), Christophe Lamaze(Centre National de la Recherche Scientifique), Pere Roca‐Cusachs(Institute for Bioengineering of Catalonia), Michael M. Kessels(Jena University Hospital), Britta Qualmann(Jena University Hospital), Marino Arroyo(Institute for Bioengineering of Catalonia), Miguel Á. del Pozo(Spanish National Centre for Cardiovascular Research)
Nature Cell Biology
December 21, 2022
Cited by 71Open Access
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Abstract

In response to different types and intensities of mechanical force, cells modulate their physical properties and adapt their plasma membrane (PM). Caveolae are PM nano-invaginations that contribute to mechanoadaptation, buffering tension changes. However, whether core caveolar proteins contribute to PM tension accommodation independently from the caveolar assembly is unknown. Here we provide experimental and computational evidence supporting that caveolin-1 confers deformability and mechanoprotection independently from caveolae, through modulation of PM curvature. Freeze-fracture electron microscopy reveals that caveolin-1 stabilizes non-caveolar invaginations-dolines-capable of responding to low-medium mechanical forces, impacting downstream mechanotransduction and conferring mechanoprotection to cells devoid of caveolae. Upon cavin-1/PTRF binding, doline size is restricted and membrane buffering is limited to relatively high forces, capable of flattening caveolae. Thus, caveolae and dolines constitute two distinct albeit complementary components of a buffering system that allows cells to adapt efficiently to a broad range of mechanical stimuli.


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