Literature DB >> 34360006

CD36 Signal Transduction in Metabolic Diseases: Novel Insights and Therapeutic Targeting.

Udayakumar Karunakaran1, Suma Elumalai1, Jun-Sung Moon1,2, Kyu-Chang Won1,2.   

Abstract

The cluster of differentiation 36 (CD36) is a scavenger receptor present on various types of cells and has multiple biological functions that may be important in inflammation and in the pathogenesis of metabolic diseases, including diabetes. Here, we consider recent insights into how the CD36 response becomes deregulated under metabolic conditions, as well as the therapeutic benefits of CD36 inhibition, which may provide clues for developing strategies aimed at the treatment or prevention of diabetes associated with metabolic diseases. To facilitate this process further, it is important to pinpoint regulatory mechanisms that are relevant under physiological and pathological conditions. In particular, understanding the mechanisms involved in dictating specific CD36 downstream cellular outcomes will aid in the discovery of potent compounds that target specific CD36 downstream signaling cascades.

Entities:  

Keywords:  CD36 antigens; diabetes mellitus; inflammation; insulin-secreting cells; oxidative stress; reactive oxygen species

Year:  2021        PMID: 34360006     DOI: 10.3390/cells10071833

Source DB:  PubMed          Journal:  Cells        ISSN: 2073-4409            Impact factor:   6.600


  2 in total

1.  Selenoprotein K contributes to CD36 subcellular trafficking in hepatocytes by accelerating nascent COPII vesicle formation and aggravates hepatic steatosis.

Authors:  Mengyue You; Fan Wu; Meilin Gao; Mengyue Chen; Shu Zeng; Yang Zhang; Wei Zhao; Danyang Li; Li Wei; Xiong Z Ruan; Yaxi Chen
Journal:  Redox Biol       Date:  2022-10-07       Impact factor: 10.787

2.  Lipotoxicity in a Vicious Cycle of Pancreatic Beta Cell Exhaustion.

Authors:  Vladimir Grubelnik; Jan Zmazek; Matej Završnik; Marko Marhl
Journal:  Biomedicines       Date:  2022-07-07
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.