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May 1, 1997Journal of Cellular Physiology113 citations

Shear stress induction of the endothelial nitric oxide synthase gene is calcium-dependent but not calcium-activated

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ZXZeshuai XiaoZZZhaohui ZhangSDScott L. Diamond

Key Result

Shear stress exposure of 4 and 25 dynes/cm2 increased the eNOS/GAPDH mRNA ratio in bovine aortic endothelial cells by 4.8- and 7.95-fold, respectively, in a calcium-dependent manner.

Structured PICO

P
Population
Cultured bovine aortic endothelial cells (BAEC)
I
Intervention
Shear stress exposure (4 and 25 dynes/cm2) for 6 hours, with or without pharmacological agents (dexamethasone, BAPTA/AM, ionomycin, genistein, tyrphostin B46, GDP-betaS)
C
Comparator
Baseline/unstimulated cells
O
Outcome
eNOS/GAPDH messenger RNA (mRNA) ratiosurrogate

Shear stress induction of eNOS mRNA in endothelial cells is a calcium-dependent but not calcium-activated process.

Main Result

Effect estimate: 4.8- and 7.95-fold increase

Abstract

Arterial levels of shear stress (25 dynes/cm2) can elevate constitutive endothelial nitric oxide synthase (eNOS) gene expression in cultured endothelial cells (Ranjan et al., 1995). By PhosphorImaging of Northern blots, we report that the eNOS/glyceraldehyde 3-phosphate dehydrogenase (GAPDH) messenger RNA (mRNA) ratio in bovine aortic endothelial cells (BAEC) increased by 4.8- and 7.95-fold after 6-hr shear stress exposure of 4 and 25 dynes/cm2, respectively. Incubation of BAEC with dexamethasone (1 microM) had no effect on shear stress induction of eNOS mRNA. Buffering of intracellular calcium in BAEC with bis-(o-aminophenoxy)-ethane-N,N,N',N'-tetraacetic acid, tetra(acetoxymethyl)-ester (BAPTA/AM) reduced shear stress induction of eNOS mRNA by 70%. Yet, stimulation of BAEC with ionomycin (0.1-1.0 microM) for 6-24 hr to elevate intracellular calcium had no effect on eNOS mRNA. These studies indicated that the shear stress induction of eNOS mRNA was a calcium-dependent, but not calcium-activated, process. Shear stress was a very potent and rapid inducer of the eNOS mRNA, which could not be mimicked with phorbol myristrate acetate or endotoxin. Inhibition of tyrosine kinases with genistein (10 microM) or tyrphostin B46 (10 microM) or inhibition of G-protein signaling with guanosine 5'-O-(2-thiodiphosphate) (GDP-betaS) (600 microM, 6-hr preincubation) did not block the shear stress elevation of eNOS mRNA.

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Cite This Study

Xiao et al. (1997) studied this question. Shear stress was evaluated on eNOS/GAPDH mRNA ratio (4.8- and 7.95-fold increase). Shear stress exposure of 4 and 25 dynes/cm2 increased the eNOS/GAPDH mRNA ratio in bovine aortic endothelial cells by 4.8- and 7.95-fold, respectively, in a calcium-dependent manner.

synapsesocial.com/papers/6a2a173d9b8d83ce413f068dhttps://doi.org/10.1002/(sici)1097-4652(199705)171:2<205::aid-jcp11>3.0.co;2-c
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