Your browser doesn't support javascript.
loading
Annexin A7 mediates lysosome repair independently of ESCRT-III.
Ebstrup, Malene Laage; Sønder, Stine Lauritzen; Fogde, Ditte Louise; Heitmann, Anne Sofie Busk; Dietrich, Tiina Naumanen; Dias, Catarina; Jäättelä, Marja; Maeda, Kenji; Nylandsted, Jesper.
Afiliação
  • Ebstrup ML; Membrane Integrity, Danish Cancer Institute, Copenhagen, Denmark.
  • Sønder SL; Membrane Integrity, Danish Cancer Institute, Copenhagen, Denmark.
  • Fogde DL; Cell Death and Metabolism, Danish Cancer Institute, Copenhagen, Denmark.
  • Heitmann ASB; Membrane Integrity, Danish Cancer Institute, Copenhagen, Denmark.
  • Dietrich TN; Bioimaging Core Facility, Danish Cancer Institute, Copenhagen, Denmark.
  • Dias C; Membrane Integrity, Danish Cancer Institute, Copenhagen, Denmark.
  • Jäättelä M; Cell Death and Metabolism, Danish Cancer Institute, Copenhagen, Denmark.
  • Maeda K; Department of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Nylandsted J; Cell Death and Metabolism, Danish Cancer Institute, Copenhagen, Denmark.
Front Cell Dev Biol ; 11: 1211498, 2023.
Article em En | MEDLINE | ID: mdl-38348092
ABSTRACT
Lysosomes are crucial organelles essential for various cellular processes, and any damage to them can severely compromise cell viability. This study uncovers a previously unrecognized function of the calcium- and phospholipid-binding protein Annexin A7 in lysosome repair, which operates independently of the Endosomal Sorting Complex Required for Transport (ESCRT) machinery. Our research reveals that Annexin A7 plays a role in repairing damaged lysosomes, different from its role in repairing the plasma membrane, where it facilitates repair through the recruitment of ESCRT-III components. Notably, our findings strongly suggest that Annexin A7, like the ESCRT machinery, is dispensable for membrane contact site formation within the newly discovered phosphoinositide-initiated membrane tethering and lipid transport (PITT) pathway. Instead, we speculate that Annexin A7 is recruited to damaged lysosomes and promotes repair through its membrane curvature and cross-linking capabilities. Our findings provide new insights into the diverse mechanisms underlying lysosomal membrane repair and highlight the multifunctional role of Annexin A7 in membrane repair.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Dinamarca