Desai Urvi, Lee E-Chiang, Chung Kyu, Gao Cuihua, Gay Jason, Key Billie, Hansen Gwenn, Machajewski Dennis, Platt Kenneth A, Sands Arthur T, Schneider Matthias, Van Sligtenhorst Isaac, Suwanichkul Adisak, Vogel Peter, Wilganowski Nat, Wingert June, Zambrowicz Brian P, Landes Greg, Powell David R
Department of Pharmaceutical Biology, Lexicon Pharmaceuticals, Inc., 8800 Technology Forest Place, The Woodlands, TX, 77381, USA.
Proc Natl Acad Sci U S A. 2007 Jul 10;104(28):11766-71. doi: 10.1073/pnas.0705041104. Epub 2007 Jul 3.
We used gene knockout mice to explore the role of Angiopoietin-like-4 (Angptl4) in lipid metabolism as well as to generate anti-Angptl4 mAbs with pharmacological activity. Angptl4 -/- mice had lower triglyceride (TG) levels resulting both from increased very low-density lipoprotein (VLDL) clearance and decreased VLDL production and had modestly lower cholesterol levels. Also, both Angptl4 -/- suckling mice and adult mice fed a high-fat diet showed reduced viability associated with lipogranulomatous lesions of the intestines and their draining lymphatics and mesenteric lymph nodes. Treating C57BL/6J, ApoE -/-, LDLr -/-, and db/db mice with the anti-Angptl4 mAb 14D12 recapitulated the lipid and histopathologic phenotypes noted in Angptl4 -/- mice. This demonstrates that the knockout phenotype reflects not only the physiologic function of the Angptl4 gene but also predicts the pharmacologic consequences of Angptl4 protein inhibition with a neutralizing antibody in relevant models of human disease.
我们使用基因敲除小鼠来探究血管生成素样蛋白4(Angptl4)在脂质代谢中的作用,并制备具有药理活性的抗Angptl4单克隆抗体。Angptl4基因敲除小鼠的甘油三酯(TG)水平较低,这是由于极低密度脂蛋白(VLDL)清除增加以及VLDL生成减少所致,其胆固醇水平也略有降低。此外,Angptl4基因敲除的哺乳期小鼠和高脂饮食喂养的成年小鼠均表现出活力下降,伴有肠道及其引流淋巴管和肠系膜淋巴结的脂肪肉芽肿性病变。用抗Angptl4单克隆抗体14D12处理C57BL/6J、ApoE基因敲除、LDLr基因敲除和db/db小鼠,重现了Angptl4基因敲除小鼠中观察到的脂质和组织病理学表型。这表明基因敲除表型不仅反映了Angptl4基因的生理功能,还预测了在人类疾病相关模型中用中和抗体抑制Angptl4蛋白的药理后果。