安格普特4
血管生成素
表型
PCSK9
脂质代谢
极低密度脂蛋白
基因剔除小鼠
载脂蛋白E
生物
内分泌学
内科学
低密度脂蛋白受体
脂蛋白
胆固醇
癌症研究
医学
受体
基因
生物化学
疾病
血管内皮生长因子
血管内皮生长因子受体
作者
Urvi Desai,E-Chiang Lee,Kyu Hyuck Chung,Cuihua Gao,Jason Gay,Billie Key,Gwenn M. Hansen,Dennis Machajewski,Kenneth A. Platt,Arthur Sands,Matthias Schneider,Jean‐Pierre Revelli,Adisak Suwanichkul,Peter Vogel,Nat Wilganowski,J. P. Wingert,Brian Zambrowicz,G M Landes,D.R. Powell
标识
DOI:10.1073/pnas.0705041104
摘要
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.
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