Canonical and non-canonical integrin-based adhesions dynamically interconvert

Adhesions are critical for anchoring cells in their environment, as signaling platforms and for cell migration. In line with these diverse functions different types of cell-matrix adhesions have been described. Best-studied are the canonical integrin-based focal adhesions. In addition, non-canonical...

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Detalles Bibliográficos
Autores: Lukas, Fabian, Matthaeus, Claudia, López Hernández, Tania, Lahmann, Ines, Schultz, Nicole, Lehmann, Martin, Puchkov, Dmytro, Pielage, Jan, Haucke, Volker, Maritzen, Tanja
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/221048
Acceso en línea:https://hdl.handle.net/2445/221048
Access Level:acceso abierto
Palabra clave:Fisiologia cel·lular
Membranes cel·lulars
Proteïnes portadores
Cell physiology
Cell membranes
Carrier proteins
Descripción
Sumario:Adhesions are critical for anchoring cells in their environment, as signaling platforms and for cell migration. In line with these diverse functions different types of cell-matrix adhesions have been described. Best-studied are the canonical integrin-based focal adhesions. In addition, non-canonical integrin adhesions lacking focal adhesion proteins have been discovered. These include reticular adhesions also known as clathrin plaques or flat clathrin lattices, that are enriched in clathrin and other endocytic proteins, as well as extensive adhesion networks and retraction fibers. How these different adhesion types that share a common integrin backbone are related and whether they can interconvert is unknown. Here, we identify the protein stonin1 as a marker for non-canonical αVβ5 integrin-based adhesions and demonstrate by live cell imaging that canonical and non-canonical adhesions can reciprocally interconvert by the selective exchange of components on a stable αVβ5 integrin scaffold. Hence, non-canonical adhesions can serve as points of origin for the generation of canonical focal adhesions.