Phospholipase C-δ1 is Activated by Capacitative Calcium Entry That Follows Phospholipase C- β Activation upon Bradykinin Stimulationopen access
- Authors
- Kim, Yong-Hyun; Park, Tae-Ju; Lee, Young Han; Baek, Kwang Jin; Suh, Pann-Ghill; Ryu, Sung Ho; Kim, Kyoung-Tai
- Issue Date
- Sep-1999
- Publisher
- AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
- Citation
- JOURNAL OF BIOLOGICAL CHEMISTRY, v.274, no.37, pp 26127 - 26134
- Pages
- 8
- Journal Title
- JOURNAL OF BIOLOGICAL CHEMISTRY
- Volume
- 274
- Number
- 37
- Start Page
- 26127
- End Page
- 26134
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/25387
- DOI
- 10.1074/jbc.274.37.26127
- ISSN
- 0021-9258
1083-351X
- Abstract
- To characterize the regulatory mechanism of phospholipase C-delta 1 (PLC-delta 1) in the bradykinin (BK) receptor-mediated signaling pathway, we used a clone of PC12 cells, which stably overexpress PLC-delta 1 (PC12-D1). Stimulation with BK induced a significantly higher Ca2+ elevation and inositol 1,4,5-trisphosphate (IP3) production with a much lower half-maximal effective concentration (EC50) of BK in PC12-D1 cells than in wild type (PC12-W) or vector-transfected (PC12-V) cells. However, BK-induced intracellular Ca2+ release and IF, generation was similar between PC12-V and PC12-D1 cells in the absence of extracellular Ca2+, suggesting that the availability of extracellular Ca2+ is essential to the activation of PLC-delta 1. When PC12-D1 cells were treated with agents that induce Ca2+ influx, more IP3 was produced, suggesting that the Ca2+ entry induces IP3 production in PC12-D1 cells. Furthermore, the additional IP3 production after BK-induced capacitative calcium entry was detected in PC12-D1 cells, suggesting that PLC-delta 1 is mainly activated by capacitative calcium entry. When cells were stimulated with BK in the presence of extracellular Ca2+, [H-3]norepinephrine secretion was much greater from PC12-D1 cells than from PC12-V cells. Our results suggest that PLC-delta 1 is activated by capacitative calcium entry following the activation of PLC-P, additively inducing IF, production and Ca2+ rise in BK-stimulated PC12 cells.
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