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LOX-1 in macrophage migration in response to ox-LDL and the involvement of calpains
被引:22
|作者:
Wang, Xianwei
[1
,2
,3
]
Ding, Zufeng
[2
,3
]
Lin, Juntang
[1
]
Guo, Zhikun
[1
]
Mehta, Jawahar L.
[2
,3
]
机构:
[1] Xinxiang Med Univ, Henan Key Lab Med Tissue Regenerat, Xinxiang, Henan, Peoples R China
[2] Univ Arkansas Med Sci, Cent Arkansas Vet Healthcare Syst, Little Rock, AR 72205 USA
[3] Univ Arkansas Med Sci, Div Cardiol, Little Rock, AR 72205 USA
基金:
中国国家自然科学基金;
关键词:
Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1);
Calpains;
Macrophage migration;
Oxidized low-density lipoprotein;
Calcium;
OXIDIZED-LDL;
COLLAGEN ACCUMULATION;
PROTEIN-KINASE;
CELL-MIGRATION;
STIMULATION;
DELETION;
RECEPTOR;
MOUSE;
D O I:
10.1016/j.bbrc.2015.09.100
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 calciumdependent 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 mu g/mL), and expression of LOX-1 and calpain-1 and -2, cell migration and intracellular calcium (Ca2+ 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 Ca2+ 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-I deletion significantly improved macrophage migration and decreased Ca2+ 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. Published by Elsevier Inc.
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页码:135 / 139
页数:5
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