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Calcium-independent phospholipase A2γ (iPLA2γ) and its roles in cellular functions and diseases.
Hara, Shuntaro; Yoda, Emiko; Sasaki, Yuka; Nakatani, Yoshihito; Kuwata, Hiroshi.
Afiliação
  • Hara S; Division of Health Chemistry, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo 142-8555, Japan. Electronic address: haras@pharm.showa-u.ac.jp.
  • Yoda E; Division of Health Chemistry, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo 142-8555, Japan.
  • Sasaki Y; Division of Health Chemistry, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo 142-8555, Japan.
  • Nakatani Y; Division of Health Chemistry, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo 142-8555, Japan.
  • Kuwata H; Division of Health Chemistry, Department of Healthcare and Regulatory Sciences, School of Pharmacy, Showa University, Tokyo 142-8555, Japan.
Biochim Biophys Acta Mol Cell Biol Lipids ; 1864(6): 861-868, 2019 06.
Article em En | MEDLINE | ID: mdl-30391710
ABSTRACT
Calcium-independent phospholipase A2γ (iPLA2γ)/patatin-like phospholipase domain-containing lipase 8 (PNPLA8) is one of the iPLA2 enzymes, which do not require Ca2+ ion for their activity. iPLA2γ is a membrane-bound enzyme with unique features, including the utilization of four distinct translation initiation sites and the presence of mitochondrial and peroxisomal localization signals. This enzyme is preferentially distributed in the mitochondria and peroxisomes and is thought to be responsible for the maintenance of lipid homeostasis in these organelles. Thus, both the overexpression and the deletion of iPLA2γ in vivo caused mitochondrial abnormalities and dysfunction. Roles of iPLA2γ in lipid mediator production and cytoprotection against oxidative stress have also been suggested by in vitro and in vivo studies. The dysregulation of iPLA2γ can therefore be a critical factor in the development of many diseases, including metabolic diseases and cancer. In this review, we provide an overview of the biochemical properties of iPLA2γ and then summarize the current understanding of the in vivo roles of iPLA2γ revealed by knockout mouse studies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cálcio / Fosfolipases A2 do Grupo IV Limite: Animals / Humans Idioma: En Revista: Biochim Biophys Acta Mol Cell Biol Lipids Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cálcio / Fosfolipases A2 do Grupo IV Limite: Animals / Humans Idioma: En Revista: Biochim Biophys Acta Mol Cell Biol Lipids Ano de publicação: 2019 Tipo de documento: Article