Carboxyl- terminal sequences in APOA5 are important for suppressing ANGPTL3/8 activity

• 成果类型: Article
• 署名作者: Chen, Yan Q.; Yang, Ye; Zhen, Eugene Y.; Beyer, Thomas P.; Li, Hongxia; Wen, Yi; Ehsani, Mariam; Jackson, Nicholas; Xie, Katherine; Jung, Hyesoo; Scheithauer, Julia L.; Kumari, Anni; Birrane, Gabriel; Russell, Anna M.; Balasubramaniam, Deepa; Liao, Zhongping; Siegel, Robert W.; Qian, Yuewei; Ploug, Michael; Young, Stephen G.; Konrad, Robert J.
• 署名单位: Eli Lilly; Lilly Research Laboratories; University of California System; University of California Los Angeles; University of California Los Angeles Medical Center; David Geffen School of Medicine at UCLA; University of California System; University of California Los Angeles; University of California Los Angeles Medical Center; David Geffen School of Medicine at UCLA; University of Copenhagen; Copenhagen University Hospital; Rigshospitalet; University of Copenhagen; Copenhagen University Hospital; Rigshospitalet; Harvard University; Harvard University Medical Affiliates; Beth Israel Deaconess Medical Center
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-13053
• DOI: 10.1073/pnas.2322332121
• 发表日期: 2024-04-23
• 关键词: apolipoprotein-a-v; activated receptor-alpha; monoclonal-antibody; lipoprotein-lipase; protein; hypertriglyceridemia; binding; serum; gene

摘要

Apolipoprotein AV (APOA5) lowers plasma triglyceride (TG) levels by binding to the binding sites within capillaries. However, the sequences in APOA5 that are required for suppressing ANGPTL3/8 activity have never been defined. A clue to the identity of those sequences was the presence of severe hypertriglyceridemia in two patients harboring an APOA5 mutation that truncates APOA5 by 35 residues (APOA5A35). We found that wild- type (WT) human APOA5, but not APOA5A35, suppressed ANGPTL3/8's ability to inhibit LPL catalytic activity. To pursue that finding, we prepared a mutant mouse APOA5 protein lacking 40 C- terminal amino acids (APOA5A40). Mouse WT- APOA5, but not APOA5A40, suppressed ANGPTL3/8's capacity to inhibit LPL catalytic activity and sharply reduced plasma TG levels in mice. WT- APOA5, but not APOA5A40, increased intracapillary LPL levels and reduced plasma TG levels in WT- APOA5, but not APOA5A40, blocked the ability of ANGPTL3/8 to detach LPL from cultured cells. Finally, an antibody against a synthetic peptide corresponding to the last 26 amino acids of mouse APOA5 reduced intracapillary LPL levels and increased plasma TG levels in WT mice. We conclude that C- terminal sequences in APOA5 are crucial for suppressing ANGPTL3/8 activity in vitro and for regulating intracapillary LPL levels and plasma TG levels in vivo.