| Literature DB >> 17609370 |
Urvi Desai1, E-Chiang Lee, Kyu Chung, Cuihua Gao, Jason Gay, Billie Key, Gwenn Hansen, Dennis Machajewski, Kenneth A Platt, Arthur T Sands, Matthias Schneider, Isaac Van Sligtenhorst, Adisak Suwanichkul, Peter Vogel, Nat Wilganowski, June Wingert, Brian P Zambrowicz, Greg Landes, David R Powell.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17609370 PMCID: PMC1913890 DOI: 10.1073/pnas.0705041104
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205