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首页> 外文期刊>Biochimica et biophysica acta: international journal of biochemistry and biophysics >The role of inorganic phosphate in regulating the kinetics of inositol 1,4,5-trisphosphate-induced Ca2+ release: a putative role for endoplasmic reticulum phosphate transporters.
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The role of inorganic phosphate in regulating the kinetics of inositol 1,4,5-trisphosphate-induced Ca2+ release: a putative role for endoplasmic reticulum phosphate transporters.

机译:无机磷酸酯在调节肌醇1,4,5-三磷酸酯诱导的Ca2 +释放动力学中的作用:内质网磷酸转运蛋白的假定作用。

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摘要

The effects of phosphate and acylphosphonate phosphate transporter inhibitors were investigated on inositol 1,4,5-trisphosphate (InsP3)-induced Ca2+ release from cerebellar microsomes. Although neither changing the phosphate concentration nor adding phosphate transporter inhibitors affected the percentage (extent) of InsP3-induced Ca2+ release, they did, however, affect the transient kinetics of this process. InsP3-induced Ca2+ release is biphasic in nature, arising from two populations of InsP3-sensitive Ca2+ stores which either release Ca2+ in a fast or slow fashion. Altering phosphate concentration or adding phosphate transporter inhibitors appeared to affect only the fast phase component. We therefore suggest that these observations could be explained by the possibility that phosphate transporters only reside in the fast releasing InsP3-sensitive Ca2+ stores.
机译:研究了磷酸盐和酰基磷酸酯磷酸盐转运蛋白抑制剂对肌醇1,4,5-三磷酸(InsP3)诱导的小脑微粒体Ca2 +释放的影响。尽管既不改变磷酸盐浓度也不添加磷酸盐转运蛋白抑制剂都不会影响InsP3诱导的Ca2 +释放的百分比(程度),但是它们确实会影响该过程的瞬态动力学。 InsP3诱导的Ca2 +释放在本质上是两相的,由两个InsP3敏感的Ca2 +存储库群引起,它们以快速或缓慢的方式释放Ca2 +。改变磷酸盐浓度或添加磷酸盐转运抑制剂似乎仅影响快相组分。因此,我们建议用磷酸盐转运蛋白仅驻留在快速释放的InsP3敏感的Ca2 +存储中的可能性来解释这些观察结果。

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