Literature DB >> 7859251

Calcium entry activated by store depletion in human umbilical vein endothelial cells.

M Oike1, M Gericke, G Droogmans, B Nilius.   

Abstract

We have used the patch clamp technique combined with simultaneous measurement of intracellular Ca2+ to record ionic currents activated by depletion of intracellular Ca(2+)-stores in endothelial cells from human umbilical veins. Two protocols were used to release Ca2+ from intracellular stores, i.e. loading of the cells via the patch pipette with Ins(1,4,5)P3, and extracellular application of thapsigargin. Ins(1,4,5)P3 (10 microM) evoked a transient increase in [Ca2+]i in cells exposed to Ca(2+)-free extracellular solutions. A subsequent reapplication of extracellular Ca2+ induced an elevation of [Ca2+]i. These changes in [Ca2+]i were very reproducible. The concomitant membrane currents were neither correlated in time nor in size with the changes in [Ca2+]i. Similar changes in [Ca2+]i and membrane currents were observed if the Ca(2+)-stores were depleted with thapsigargin. Activation of these currents was prevented and holding currents at -40 mV were small if store depletion was induced in the presence of 50 microM NPPB. This identifies the large currents, which are activated as a consequence of store-depletion, as mechanically activated Cl- currents, which have been described previously [1,2]. Loading the cells with Ins(1,4,5)P3 together with 10 mM BAPTA induced only a very short lasting Ca2+ transient, which was not accompanied by activation of a detectable current, even in a 10 mM Ca(2+)-containing extracellular solution. Also thapsigargin does not activate any membrane current if the pipette solution contains 10 mM BAPTA (ruptured patches). The contribution of Ca(2+)-influx to the membrane current during reapplication of 10 mM extracellular calcium to thapsigargin-pretreated cells was estimated from the first time derivative of the corresponding Ca2+ transients at different holding potentials. These current values showed strong inward rectification, with a maximal amplitude of 1.0 +/- 0.3 pA at -80 mV (n = 8; membrane capacitance 59 +/- 9 pF).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7859251     DOI: 10.1016/0143-4160(94)90030-2

Source DB:  PubMed          Journal:  Cell Calcium        ISSN: 0143-4160            Impact factor:   6.817


  14 in total

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Journal:  Br J Pharmacol       Date:  2007-09-17       Impact factor: 8.739

2.  Calcium-activated chloride channels in bovine pulmonary artery endothelial cells.

Authors:  B Nilius; J Prenen; G Szücs; L Wei; F Tanzi; T Voets; G Droogmans
Journal:  J Physiol       Date:  1997-01-15       Impact factor: 5.182

3.  Smooth muscle membrane potential modulates endothelium-dependent relaxation of rat basilar artery via myo-endothelial gap junctions.

Authors:  Tracy Allen; Mircea Iftinca; William C Cole; Frances Plane
Journal:  J Physiol       Date:  2002-12-15       Impact factor: 5.182

4.  Properties of heterologously expressed hTRP3 channels in bovine pulmonary artery endothelial cells.

Authors:  M Kamouchi; S Philipp; V Flockerzi; U Wissenbach; A Mamin; L Raeymaekers; J Eggermont; G Droogmans; B Nilius
Journal:  J Physiol       Date:  1999-07-15       Impact factor: 5.182

Review 5.  CRAC channelopathies.

Authors:  Stefan Feske
Journal:  Pflugers Arch       Date:  2010-01-29       Impact factor: 3.657

6.  Chloride-sensitive nature of the histamine-induced Ca2+ entry in cultured human aortic endothelial cells.

Authors:  K Ono; M Nakao; T Iijima
Journal:  J Physiol       Date:  1998-09-15       Impact factor: 5.182

7.  Ca2+ influx induced by store release and cytosolic Ca2+ chelation in Ht29 colonic carcinoma cells.

Authors:  G Kerst; K G Fischer; C Normann; A Kramer; J Leipziger; R Greger
Journal:  Pflugers Arch       Date:  1995-09       Impact factor: 3.657

8.  STIM1/Orai1, ICRAC, and endothelial SOC.

Authors:  Mohamed Trebak
Journal:  Circ Res       Date:  2009-05-08       Impact factor: 17.367

9.  Stim1 and Orai1 mediate CRAC currents and store-operated calcium entry important for endothelial cell proliferation.

Authors:  Iskandar F Abdullaev; Jonathan M Bisaillon; Marie Potier; Jose C Gonzalez; Rajender K Motiani; Mohamed Trebak
Journal:  Circ Res       Date:  2008-10-09       Impact factor: 17.367

10.  In the presence of L-NAME SERCA blockade induces endothelium-dependent contraction of mouse aorta through activation of smooth muscle prostaglandin H2/thromboxane A2 receptors.

Authors:  Elena B Okon; Ali Golbabaie; Cornelis van Breemen
Journal:  Br J Pharmacol       Date:  2002-10       Impact factor: 8.739

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