Literature DB >> 32705602

CGI-58: Versatile Regulator of Intracellular Lipid Droplet Homeostasis.

Liqing Yu1, Yi Li2, Alison Grisé3, Huan Wang2.   

Abstract

Comparative gene identification-58 (CGI-58), also known as α/β-hydrolase domain-containing 5 (ABHD5), is a member of a large family of proteins containing an α/β-hydrolase-fold. CGI-58 is well-known as the co-activator of adipose triglyceride lipase (ATGL), which is a key enzyme initiating cytosolic lipid droplet lipolysis. Mutations in either the human CGI-58 or ATGL gene cause an autosomal recessive neutral lipid storage disease, characterized by the excessive accumulation of triglyceride (TAG)-rich lipid droplets in the cytoplasm of almost all cell types. CGI-58, however, has ATGL-independent functions. Distinct phenotypes associated with CGI-58 deficiency commonly include ichthyosis (scaly dry skin), nonalcoholic steatohepatitis, and hepatic fibrosis. Through regulated interactions with multiple protein families, CGI-58 controls many metabolic and signaling pathways, such as lipid and glucose metabolism, energy balance, insulin signaling, inflammatory responses, and thermogenesis. Recent studies have shown that CGI-58 regulates the pathogenesis of common metabolic diseases in a tissue-specific manner. Future studies are needed to molecularly define ATGL-independent functions of CGI-58, including the newly identified serine protease activity of CGI-58. Elucidation of these versatile functions of CGI-58 may uncover fundamental cellular processes governing lipid and energy homeostasis, which may help develop novel approaches that counter against obesity and its associated metabolic sequelae.

Entities:  

Keywords:  ATGL; CGI-58; Lipid droplet; Lipolysis

Mesh:

Substances:

Year:  2020        PMID: 32705602      PMCID: PMC8063591          DOI: 10.1007/978-981-15-6082-8_13

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  264 in total

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4.  Macrophage CGI-58 Attenuates Inflammatory Responsiveness via Promotion of PPARγ Signaling.

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Authors:  James G Granneman; Hsiao-Ping H Moore; Rukmani Krishnamoorthy; Miloni Rathod
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10.  Human frame shift mutations affecting the carboxyl terminus of perilipin increase lipolysis by failing to sequester the adipose triglyceride lipase (ATGL) coactivator AB-hydrolase-containing 5 (ABHD5).

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  6 in total

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