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.
机构:
Tokyo Metropolitan Tama Med Ctr, Dept Neurosurg, 2-8-29 Musashi Dai, Fuchu, Tokyo 1838524, JapanTokyo Metropolitan Tama Med Ctr, Dept Neurosurg, 2-8-29 Musashi Dai, Fuchu, Tokyo 1838524, Japan
Ota, Takahiro
Komiyama, Masaki
论文数: 0引用数: 0
h-index: 0
机构:
Osaka City Gen Hosp, Dept Neurointervent, Osaka, JapanTokyo Metropolitan Tama Med Ctr, Dept Neurosurg, 2-8-29 Musashi Dai, Fuchu, Tokyo 1838524, Japan