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Phosphatidylserine regulates plasma membrane repair through tetraspanin-enriched macrodomains.
Li, Yang E; Norris, Dougall M; Xiao, Fanqian N; Pandzic, Elvis; Whan, Renee M; Fok, Sandra; Zhou, Ming; Du, Guangwei; Liu, Yang; Du, Ximing; Yang, Hongyuan.
Afiliação
  • Li YE; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.
  • Norris DM; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.
  • Xiao FN; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.
  • Pandzic E; Katerina Gaus Light Microscopy Facility, Mark Wainwright Analytical Center, University of New South Wales, Sydney, Australia.
  • Whan RM; Katerina Gaus Light Microscopy Facility, Mark Wainwright Analytical Center, University of New South Wales, Sydney, Australia.
  • Fok S; Katerina Gaus Light Microscopy Facility, Mark Wainwright Analytical Center, University of New South Wales, Sydney, Australia.
  • Zhou M; Verna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX, USA.
  • Du G; Department of Integrative Biology and Pharmacology, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Liu Y; Department of Integrative Biology and Pharmacology, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Du X; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.
  • Yang H; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, Australia.
J Cell Biol ; 223(6)2024 Jun 03.
Article em En | MEDLINE | ID: mdl-38530252
ABSTRACT
The integrity of the plasma membrane is critical to cell function and survival. Cells have developed multiple mechanisms to repair damaged plasma membranes. A key process during plasma membrane repair is to limit the size of the damage, which is facilitated by the presence of tetraspanin-enriched rings surrounding damage sites. Here, we identify phosphatidylserine-enriched rings surrounding damaged sites of the plasma membrane, resembling tetraspanin-enriched rings. Importantly, the formation of both the phosphatidylserine- and tetraspanin-enriched rings requires phosphatidylserine and its transfer proteins ORP5 and ORP9. Interestingly, ORP9, but not ORP5, is recruited to the damage sites, suggesting cells acquire phosphatidylserine from multiple sources upon plasma membrane damage. We further demonstrate that ORP9 contributes to efficient plasma membrane repair. Our results thus unveil a role for phosphatidylserine and its transfer proteins in facilitating the formation of tetraspanin-enriched macrodomains and plasma membrane repair.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilserinas / Membrana Celular / Tetraspaninas Limite: Humans Idioma: En Revista: J Cell Biol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfatidilserinas / Membrana Celular / Tetraspaninas Limite: Humans Idioma: En Revista: J Cell Biol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália