Extracellular ATP mobilizes intracellular Ca2+ in T51B rat liver epithelial cells: a study involving single cell measurements.
Extracellular ATP mobilizes intracellular Ca2+ in T51B rat liver epithelial cells: a study involving single cell measurements.
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细胞外 ATP 在 T51B 大鼠肝上皮细胞中动员细胞内 Ca2:一项涉及单细胞测量的研究。
DOI:
10.1016/0014-4827(89)90198-5
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发表时间:
1989
影响因子:
3.7
通讯作者:
Berggren,PO
中科院分区:
文献类型:
--
作者:
Boynton,AL;Cooney,RV;Hill,TD;Nilsson,T;Arkhammar,P;Berggren,PO
T51B rat liver epithelial cells were stimulated with extracellular ATP. Changes in cytoplasmic free Ca2+concentration ([Ca2*]i) were measured by fura-2 both in a large population of cells on coverslips in a cuvette and in single cells in a microscopic system. Extracellular ATP evoked a prompt increase in [Ca2+]iin both the presence and absence of extracellular Ca2+, although the effect was less pronounced in the latter case. These findings indicate that at least part of the [Ca2+]iincrease is due to mobilization of intracellularly bound calcium. Stimulation with ATP did not mobilize the total pool of intracellular releasable Ca2+, as evidenced from experiments where subsequent addition of ionomycin evoked a pronounced increase in [Ca2+]iin the absence of extracellular Ca2+. The effect of ATP was maintained at room temperature but was markedly impaired in the absence of continuous stirring of the buffer solution. In the absence of stirring, ATP had to be increased to the millimolar range in order to evoke a pronounced effect. Single cell measurements revealed a heterogenous Ca2+response to ATP, with some cells failing to respond with a detectable increase in [Ca2+]i. The actual increase in [Ca2+]iwas not uniform throughout the cytoplasm, but seemed to start in one part of the cell. Even if part of the [Ca2+]iincrease might be accounted for by ATP promoting the hydrolysis of phosphatidylinositol 4,5-bisphosphate and thereby a generation of InsP3and diacylglycerol, there was no initiation of DNA synthesis under the present conditions. Hence, extracellular growth factors exert either a quantitative difference in second messenger production or additional stimulatory effects by activating intracellular signal pathways beyond these represented by [Ca2+]iand protein kinase C.
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影响因子:
3.7
作者:
A. Boynton;L. Kleine;J. Whitfield;D. Bossi
通讯作者:
D. Bossi
影响因子:
4.8
作者:
K. Chang;P. Cuatrecasas
通讯作者:
P. Cuatrecasas
影响因子:
5.5
作者:
COCKCROFT, S;GOMPERTS, BD
通讯作者:
GOMPERTS, BD
影响因子:
4.8
作者:
S. Pirotton;Eric Raspé;D. Demolle;Christophe Erneux;J. Boeynaems
通讯作者:
J. Boeynaems
影响因子:
4.1
作者:
Y. Landry;A. Lehninger
通讯作者:
A. Lehninger