Wang Xianwei, Ding Zufeng, Lin Juntang, Guo Zhikun, Mehta Jawahar L
Henan Key Laboratory of Medical Tissue Regeneration, Xinxiang Medical University, Xinxiang, Henan, China; Central Arkansas Veterans Healthcare System, and the Division of Cardiology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Central Arkansas Veterans Healthcare System, and the Division of Cardiology, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Biochem Biophys Res Commun. 2015 Nov 6;467(1):135-9. doi: 10.1016/j.bbrc.2015.09.100. Epub 2015 Sep 21.
Previous studies have shown that oxidized low-density lipoprotein (ox-LDL) inhibits macrophage migration, but the precise mechanisms remain unclear. Lectin-like ox-LDL receptor-1 (LOX-1) is a scavenger receptor that is expressed in macrophages and binds ox-LDL. Calpains, a family of calcium-dependent proteases, influence several aspects of cell migration. In this study, we investigated the role of LOX-1 in macrophage migration in response to ox-LDL and the involvement of calpains in this process. Peritoneal macrophages from wild type C57BL/6 mice were exposed to different concentrations of ox-LDL (1-20 μg/mL), and expression of LOX-1 and calpain-1 and -2, cell migration and intracellular calcium (Ca(2+)in) were measured. Our results showed that ox-LDL stimulated LOX-1 and calpain-2 expression, and inhibited calpain-1 expression in a dose- and time-dependent manner. Further, ox-LDL inhibited macrophage migration and increased Ca(2+)in concentration in macrophages. To further elucidate the role of LOX-1 in ox-LDL-impaired macrophage migration, we isolated peritoneal macrophages from LOX-1 knockout mice, and treated them with ox-LDL. Interestingly, calpain-1 expression was much higher, and calpain-2 expression was lower in LOX-1 knockout macrophages than in wild-type macrophages following exposure to ox-LDL. LOX-1 deletion significantly improved macrophage migration and decreased Ca(2+)in concentration. These data indicate that LOX-1 is, at least in part, responsible for the inhibitory effect of ox-LDL on macrophage migration and this process involves calpain-1 and -2.
先前的研究表明,氧化型低密度脂蛋白(ox-LDL)会抑制巨噬细胞迁移,但其确切机制仍不清楚。凝集素样氧化型低密度脂蛋白受体-1(LOX-1)是一种清道夫受体,在巨噬细胞中表达并与ox-LDL结合。钙蛋白酶是一类钙依赖性蛋白酶,会影响细胞迁移的多个方面。在本研究中,我们调查了LOX-1在巨噬细胞对ox-LDL反应性迁移中的作用以及钙蛋白酶在此过程中的参与情况。将野生型C57BL/6小鼠的腹腔巨噬细胞暴露于不同浓度的ox-LDL(1-20μg/mL),并检测LOX-1、钙蛋白酶-1和-2的表达、细胞迁移以及细胞内钙(Ca(2+)in)。我们的结果表明,ox-LDL以剂量和时间依赖性方式刺激LOX-1和钙蛋白酶-2的表达,并抑制钙蛋白酶-1的表达。此外,ox-LDL抑制巨噬细胞迁移并增加巨噬细胞中的Ca(2+)in浓度。为了进一步阐明LOX-1在ox-LDL损害的巨噬细胞迁移中的作用,我们从LOX-1基因敲除小鼠中分离出腹腔巨噬细胞,并用ox-LDL处理它们。有趣的是,暴露于ox-LDL后,LOX-1基因敲除巨噬细胞中的钙蛋白酶-1表达明显更高,而钙蛋白酶-2表达则低于野生型巨噬细胞。LOX-1缺失显著改善了巨噬细胞迁移并降低了Ca(2+)in浓度。这些数据表明,LOX-1至少部分负责ox-LDL对巨噬细胞迁移的抑制作用,并且这一过程涉及钙蛋白酶-1和-2。