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Ca(2+) -钙调蛋白参与血小板衍生生长因子、成纤维细胞生长因子和胰岛素诱导NIH - 3T3细胞中的鸟氨酸脱羧酶活性。

Involvement of Ca(2+)-calmodulin in platelet-derived growth factor-, fibroblast growth factor-, and insulin-induced ornithine decarboxylase in NIH-3T3 cells.

作者信息

Katori T, Yasuda H, Fukuda H, Kimura S

机构信息

First Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.

出版信息

Metabolism. 1994 Jan;43(1):4-10. doi: 10.1016/0026-0495(94)90150-3.

DOI:10.1016/0026-0495(94)90150-3
PMID:8289674
Abstract

Ornithine decarboxylase (ODC) was induced by platelet-derived growth factor (PDGF), fibroblast growth factor (FGF), and insulin at doses ranging from 0.125 to 0.5 U/mL, 25 to 500 ng/mL, and 10(-8) to 10(-7) mol/L, respectively, in NIH-3T3 cells. The induction of ODC reached a plateau approximately 4 to 6 hours after addition of each mitogen. PDGF exerted a synergistic action with 10(-7) mol/L insulin until the concentration of PDGF reached 0.5 U/mL and exerted an additive action at concentrations greater than 0.5 U/mL. FGF also accelerated ODC induction by insulin (10(-7) mol/L) synergistically when it was added at doses up to 500 ng/mL. PDGF added to the intact monolayer cells caused a spike-and-plateau increase in cytosolic Ca2+ concentration ([Ca2+]i); the spike was independent of extracellular Ca2+, whereas the plateau formation was dependent on extracellular Ca2+. On the other hand, FGF caused a plateau-like increase in [Ca2+]i, exclusively dependent on extracellular Ca2+. Insulin did not affect [Ca2+]i in NIH-3T3 cells. Trifluoperazine (15 to 30 mumol/L) inhibited the induction of ODC by PDGF and FGF, but did not inhibit the effect of insulin to induce ODC. N-(6-aminohexyl)-5-chloro-1-Naphthalenesulfonamide ([W-7] 30 to 40 mumol/L) showed a more profound suppressive effect on ODC induced by PDGF and FGF than N-(6-aminohexyl)-naphthalenesulfonamide (W-5) did. There was no difference between the effects of W-7 and W-5 on ODC induction by insulin.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在NIH-3T3细胞中,鸟氨酸脱羧酶(ODC)分别被血小板衍生生长因子(PDGF)、成纤维细胞生长因子(FGF)和胰岛素诱导,诱导剂量范围分别为0.125至0.5 U/mL、25至500 ng/mL和10⁻⁸至10⁻⁷ mol/L。在添加每种促分裂原后约4至6小时,ODC的诱导达到平台期。PDGF与10⁻⁷ mol/L胰岛素发挥协同作用,直至PDGF浓度达到0.5 U/mL,而在浓度大于0.5 U/mL时发挥相加作用。当以高达500 ng/mL的剂量添加时,FGF也与胰岛素(10⁻⁷ mol/L)协同加速ODC诱导。添加到完整单层细胞中的PDGF导致胞质Ca²⁺浓度([Ca²⁺]i)出现尖峰和平台期升高;尖峰独立于细胞外Ca²⁺,而平台期形成依赖于细胞外Ca²⁺。另一方面,FGF导致[Ca²⁺]i出现类似平台期的升高,完全依赖于细胞外Ca²⁺。胰岛素不影响NIH-3T3细胞中的[Ca²⁺]i。三氟拉嗪(15至30 μmol/L)抑制PDGF和FGF对ODC的诱导,但不抑制胰岛素诱导ODC的作用。N-(6-氨基己基)-5-氯-1-萘磺酰胺([W-7] 30至40 μmol/L)对PDGF和FGF诱导的ODC的抑制作用比N-(6-氨基己基)-萘磺酰胺(W-5)更显著。W-7和W-5对胰岛素诱导ODC的作用无差异。(摘要截短于250字)

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