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大鼠肝细胞中受体介导的锰离子内流:用Fura-2酯负载的细胞与显微注射Fura-2盐的细胞的比较。

Receptor-mediated Mn2+ influx in rat hepatocytes: comparison of cells loaded with Fura-2 ester and cells microinjected with Fura-2 salt.

作者信息

Kass G E, Webb D L, Chow S C, Llopis J, Berggren P O

机构信息

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

Biochem J. 1994 Aug 15;302 ( Pt 1)(Pt 1):5-9. doi: 10.1042/bj3020005.

DOI:10.1042/bj3020005
PMID:8068023
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1137183/
Abstract

In single Fura-2 ester-loaded hepatocytes, stimulation by vasopressin, but not emptying of the agonist-sensitive Ca2+ store by 2,5-di-(t-butyl)hydroquinone, resulted in an increase in the rate of Fura-2 fluorescence-quenching by Mn2+. Similarly, in cells microinjected with Fura-2 salt, vasopressin stimulated Mn2+ entry while 2,5-di-(t-butyl)hydroquinone or thapsigargin did not. The pattern of Fura-2 quenching by Mn2+ only correlated with the movement of Mn2+ across the plasma membrane.

摘要

在单个负载Fura-2酯的肝细胞中,血管加压素刺激可导致Mn2+引起的Fura-2荧光猝灭速率增加,而2,5-二(叔丁基)对苯二酚排空激动剂敏感的Ca2+储存库则不会。同样,在显微注射Fura-2盐的细胞中,血管加压素刺激Mn2+内流,而2,5-二(叔丁基)对苯二酚或毒胡萝卜素则无此作用。Mn2+引起的Fura-2猝灭模式仅与Mn2+跨质膜的移动相关。

相似文献

1
Receptor-mediated Mn2+ influx in rat hepatocytes: comparison of cells loaded with Fura-2 ester and cells microinjected with Fura-2 salt.大鼠肝细胞中受体介导的锰离子内流:用Fura-2酯负载的细胞与显微注射Fura-2盐的细胞的比较。
Biochem J. 1994 Aug 15;302 ( Pt 1)(Pt 1):5-9. doi: 10.1042/bj3020005.
2
Actions of vasopressin and the Ca(2+)-ATPase inhibitor, thapsigargin, on Ca2+ signaling in hepatocytes.血管加压素和Ca(2+)-ATP酶抑制剂毒胡萝卜素对肝细胞中Ca2+信号传导的作用。
J Biol Chem. 1992 Apr 25;267(12):8230-3.
3
Receptor-operated calcium influx in rat hepatocytes. Identification and characterization using manganese.大鼠肝细胞中受体介导的钙内流。利用锰进行鉴定和表征
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4
Evidence for two pathways of receptor-mediated Ca2+ entry in hepatocytes.肝细胞中受体介导的钙离子内流两条途径的证据。
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5
Calcium influx evoked by Ca2+ store depletion in human platelets is more susceptible to cytochrome P-450 inhibitors than receptor-mediated calcium entry.与受体介导的钙内流相比,人血小板中由Ca2+ 储存耗竭引起的钙内流对细胞色素P - 450抑制剂更敏感。
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Inositol 1,4,5-trisphosphate activates receptor-mediated calcium entry by two different pathways in hepatocytes.肌醇1,4,5-三磷酸通过两种不同途径激活肝细胞中受体介导的钙内流。
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Differentiation of BC3H1 smooth muscle cells changes the bivalent cation selectivity of the capacitative Ca2+ entry pathway.BC3H1平滑肌细胞的分化改变了容量性Ca2+内流途径的二价阳离子选择性。
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8
Vasopressin stimulation of Ca2+ mobilization, two bivalent cation entry pathways and Ca2+ efflux in A7r5 rat smooth muscle cells.血管加压素对A7r5大鼠平滑肌细胞中Ca2+动员、两条二价阳离子进入途径及Ca2+外流的刺激作用。
J Physiol. 1995 Jun 1;485 ( Pt 2)(Pt 2):455-68. doi: 10.1113/jphysiol.1995.sp020742.

本文引用的文献

1
Intracellular calcium mobilization by inositol 1,4,5-trisphosphate: intracellular movements and compartmentalization.肌醇1,4,5-三磷酸介导的细胞内钙动员:细胞内转运与区室化
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Inhibition of thapsigargin-induced calcium entry by microinjected guanine nucleotide analogues. Evidence for the involvement of a small G-protein in capacitative calcium entry.显微注射鸟嘌呤核苷酸类似物对毒胡萝卜素诱导的钙内流的抑制作用。小G蛋白参与容量性钙内流的证据。
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A GTP-dependent step in the activation mechanism of capacitative calcium influx.钙库操纵性钙内流激活机制中一个依赖鸟苷三磷酸(GTP)的步骤。
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Depletion of InsP3 stores activates a Ca2+ and K+ current by means of a phosphatase and a diffusible messenger.肌醇三磷酸(InsP3)储存的耗尽通过一种磷酸酶和一种可扩散信使激活钙电流和钾电流。
Nature. 1993 Aug 26;364(6440):814-8. doi: 10.1038/364814a0.
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Multiple mechanisms by which protein kinase A potentiates inositol 1,4,5-trisphosphate-induced Ca2+ mobilization in permeabilized hepatocytes.蛋白激酶A增强通透化肝细胞中肌醇1,4,5-三磷酸诱导的Ca2+动员的多种机制。
Biochem J. 1993 Jul 15;293 ( Pt 2)(Pt 2):413-22. doi: 10.1042/bj2930413.
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Verapamil and diltiazem inhibit receptor-operated calcium channels and intracellular calcium oscillations in rat hepatocytes.维拉帕米和地尔硫䓬抑制大鼠肝细胞中的受体操纵性钙通道和细胞内钙振荡。
FEBS Lett. 1993 Mar 8;318(3):341-4. doi: 10.1016/0014-5793(93)80542-3.
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Inositol trisphosphate and calcium signalling.肌醇三磷酸与钙信号传导
Nature. 1993 Jan 28;361(6410):315-25. doi: 10.1038/361315a0.
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Emptying of intracellular Ca2+ stores releases a novel small messenger that stimulates Ca2+ influx.细胞内钙库排空会释放一种新型小分子信使,该信使可刺激钙内流。
Nature. 1993 Aug 26;364(6440):809-14. doi: 10.1038/364809a0.
9
Two independently regulated Ca2+ entry mechanisms coexist in Jurkat T cells during T cell receptor antigen activation.在T细胞受体抗原激活过程中,两种独立调节的Ca2+内流机制共存于Jurkat T细胞中。
Biochem J. 1993 Jul 15;293 ( Pt 2)(Pt 2):395-8. doi: 10.1042/bj2930395.
10
Multiple mechanisms of manganese-induced quenching of fura-2 fluorescence in rat mast cells.锰诱导大鼠肥大细胞中fura-2荧光淬灭的多种机制。
Pflugers Arch. 1993 May;423(3-4):225-31. doi: 10.1007/BF00374399.