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Gasdermins: pore-forming activities and beyond.
Zheng, Zengzhang; Deng, Wanyan; Lou, Xiwen; Bai, Yang; Wang, Junhong; Zeng, Huasong; Gong, Sitang; Liu, Xing.
Afiliação
  • Zheng Z; The Joint Center for Infection and Immunity between Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou, 510623, China.
  • Deng W; Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
  • Lou X; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
  • Bai Y; The Joint Center for Infection and Immunity between Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou, 510623, China.
  • Wang J; Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
  • Zeng H; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
  • Gong S; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
  • Liu X; The Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
Acta Biochim Biophys Sin (Shanghai) ; 52(5): 467-474, 2020 May 26.
Article em En | MEDLINE | ID: mdl-32294153
ABSTRACT
Gasdermins (GSDMs) belong to a protein superfamily that is found only in vertebrates and consists of GSDMA, GSDMB, GSDMC, GSDMD, DFNA5 (a.k.a. GSDME) and DFNB59 (a.k.a. Pejvakin (PJVK)) in humans. Except for DFNB59, all members of the GSDM superfamily contain a conserved two-domain structure (N-terminal and C-terminal domains) and share an autoinhibitory mechanism. When the N-terminal domain of these GSDMs is released, it possesses pore-forming activity that causes inflammatory death associated with the loss of cell membrane integrity and release of inflammatory mediators. It has also been found that spontaneous mutations occurring in the genes of GSDMs have been associated with the development of certain autoimmune disorders, as well as cancers. Here, we review the current knowledge of the expression profile and regulation of GSDMs and the important roles of this protein family in inflammatory cell death, tumorigenesis and other related diseases.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Membrana Celular / Carcinogênese / Proteínas de Neoplasias / Neoplasias Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Membrana Celular / Carcinogênese / Proteínas de Neoplasias / Neoplasias Idioma: En Ano de publicação: 2020 Tipo de documento: Article