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Double life: How GRK2 and ß-arrestin signaling participate in diseases.
Zhai, Ruxu; Snyder, Jonathan; Montgomery, Sarah; Sato, Priscila Y.
Afiliação
  • Zhai R; Drexel University College of Medicine, Department of Pharmacology and Physiology, Philadelphia, PA, USA.
  • Snyder J; Drexel University College of Medicine, Department of Pharmacology and Physiology, Philadelphia, PA, USA.
  • Montgomery S; Drexel University College of Medicine, Department of Pharmacology and Physiology, Philadelphia, PA, USA.
  • Sato PY; Drexel University College of Medicine, Department of Pharmacology and Physiology, Philadelphia, PA, USA. Electronic address: pys26@drexel.edu.
Cell Signal ; 94: 110333, 2022 06.
Article em En | MEDLINE | ID: mdl-35430346
ABSTRACT
G-protein coupled receptor (GPCR) kinases (GRKs) and ß-arrestins play key roles in GPCR and non-GPCR cellular responses. In fact, GRKs and arrestins are involved in a plethora of pathways vital for physiological maintenance of inter- and intracellular communication. Here we review decades of research literature spanning from the discovery, identification of key structural elements, and findings supporting the diverse roles of these proteins in GPCR-mediated pathways. We then describe how GRK2 and ß-arrestins partake in non-GPCR signaling and briefly summarize their involvement in various pathologies. We conclude by presenting gaps in knowledge and our prospective on the promising pharmacological potential in targeting these proteins and/or downstream signaling. Future research is warranted and paramount for untangling these novel and promising roles for GRK2 and arrestins in metabolism and disease progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arrestinas / Quinases de Receptores Acoplados a Proteína G Tipo de estudo: Prognostic_studies Idioma: En Revista: Cell Signal Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arrestinas / Quinases de Receptores Acoplados a Proteína G Tipo de estudo: Prognostic_studies Idioma: En Revista: Cell Signal Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos