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Journal of Lipid Research
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    • Research Article
      Open Access

      Atherosclerosis-associated hepatic secretion of VLDL but not PCSK9 is dependent on cargo receptor protein Surf4

      Journal of Lipid Research
      Vol. 62100091Published online: June 9, 2021
      • Bingxiang Wang
      • Yishi Shen
      • Lei Zhai
      • Xiaodan Xia
      • Hong-mei Gu
      • Maggie Wang
      • and others
      Cited in Scopus: 0
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        Plasma LDL is produced from catabolism of VLDL and cleared from circulation mainly via the hepatic LDL receptor (LDLR). Proprotein convertase subtilisin/kexin type 9 (PCSK9) promotes LDLR degradation, increasing plasma LDL-C levels. Circulating PCSK9 is mainly secreted by the liver, whereas VLDL is exclusively secreted by hepatocytes. However, the mechanism regulating their secretion is not completely understood. Surfeit 4 (Surf4) is a cargo receptor localized in the ER membrane. It recruits cargos into coat protein complex II vesicles to facilitate their secretion.
        Atherosclerosis-associated hepatic secretion of VLDL but not PCSK9 is dependent on cargo receptor protein Surf4
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