Homocysteine enhances cardiac neural crest cell attachment in vitro by increasing intracellular calcium levels

被引:9
|
作者
Heidenreich, David J.
Reedy, Mark V. [2 ]
Brauer, Philip R. [1 ]
机构
[1] Creighton Univ, Dept Biomed Sci, Sch Med, Omaha, NE 68178 USA
[2] Creighton Univ, Dept Biol, Omaha, NE 68178 USA
关键词
neural crest; homocysteine; calcium signaling; cell attachment; morphogenesis;
D O I
10.1002/dvdy.21644
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Elevated homocysteine (Hcys) increases the risk of neurocristopathies. Previous studies show Hcys inhibits neural crest (NQ cell migration in vivo. However, the mechanisms responsible for this effect are unknown. Here, we evaluated the effect of Hcys on NC cell attachment in vitro and determined if any of the effects were due to altered Ca(2+) signaling. We found Hcys enhanced NC cell attachment in a dose and substrate-dependent manner. lonomycin mimicked the effect of Hcys while BAPTA-AM and 2-APB blocked the effect of Hcys on NC attachment. In contrast, inhibitors of plasma membrane Ca(2+) channels had no effect on NC attachment. Hcys also increased the emission of the intracellular Ca(2+) -sensitive probe, Fluo-4. These results show Hcys alters NC attachment by triggering an increase in intracellular Ca(2+) possibly by generating inositol triphosphate. Hence, the teratogenic effect ascribed to Hcys may be due to perturbation of intracellular Ca(2+) signaling.
引用
收藏
页码:2117 / 2128
页数:12
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