泡沫电池
清道夫受体
磷酸化
食腐动物
化学
巨噬细胞
激酶
受体
细胞生物学
脂蛋白
细胞
载脂蛋白E
体外
生物化学
胆固醇
内科学
生物
激进的
医学
疾病
作者
Roméo Ricci,Grzegorz Sumara,Izabela Sumara,Izabela Rozenberg,Michael Kurrer,Alexander Akhmedov,Martin Hersberger,Urs Eriksson,Franz R. Eberli,Burkhard Becher,Jan Borén,Mian Chen,Myron I. Cybulsky,Kathryn J. Moore,Mason W. Freeman,Erwin F. Wagner,Christian M. Matter,Thomas F. Lüscher
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2004-11-26
卷期号:306 (5701): 1558-1561
被引量:257
标识
DOI:10.1126/science.1101909
摘要
In vitro studies suggest a role for c-Jun N-terminal kinases (JNKs) in proatherogenic cellular processes. We show that atherosclerosis-prone ApoE-/- mice simultaneously lacking JNK2 (ApoE-/- JNK2-/- mice), but not ApoE-/- JNK1-/- mice, developed less atherosclerosis than do ApoE-/- mice. Pharmacological inhibition of JNK activity efficiently reduced plaque formation. Macrophages lacking JNK2 displayed suppressed foam cell formation caused by defective uptake and degradation of modified lipoproteins and showed increased amounts of the modified lipoprotein-binding and -internalizing scavenger receptor A (SR-A), whose phosphorylation was markedly decreased. Macrophage-restricted deletion of JNK2 was sufficient to decrease atherogenesis. Thus, JNK2-dependent phosphorylation of SR-A promotes uptake of lipids in macrophages, thereby regulating foam cell formation, a critical step in atherogenesis.
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