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细胞钙在α-1肾上腺素能受体调控棕色脂肪细胞花生四烯酸释放中的作用。

Role of cell calcium in alpha-1 adrenergic receptor control of arachidonic acid release from brown adipocytes.

作者信息

Schimmel R J

机构信息

Department of Physiology, UMDNJ-School of Osteopathic Medicine, Robert Wood Johnson Medical School, Piscataway 08854.

出版信息

Cell Signal. 1989;1(6):607-16. doi: 10.1016/0898-6568(89)90069-7.

Abstract

Exposure of brown fat cells to phenylephrine, an agonist of alpha-1 adrenergic receptors, activates a phospholipase A2 which releases arachidonic acid. Since receptor activation of phospholipase A2 requires calcium, experiments were undertaken to define more precisely the role played by calcium in the regulation of enzyme activity. In this study, adipocytes were loaded with the fluorescent calcium chelator quin2 in order to buffer intracellular calcium and block receptor stimulated changes in its concentration. When quin2 loaded adipocytes were incubated in buffer containing 0.10 mM calcium, the ability of phenylephrine to stimulate release of arachidonic acid was severely reduced. At an intracellular quin2 concentration of 6.6 mM stimulated arachidonic acid release was inhibited by more than 50% and at 13 mM it was completely blocked. In contrast, phenylephrine stimulation of inositol phosphate accumulation was unaffected by quin2. Quin2 also did not affect the liberation of arachidonic acid in response to exogenous phospholipase C, A23187 or forskolin. The intracellular calcium antagonist TMB-8 also inhibited phenylephrine-stimulation of arachidonic acid release and this effect was reversed by ionomycin. Basal phospholipase A2 activity was increased by introduction of high calcium concentrations into cells rendered permeable with digitonin, but phenylephrine still caused a further increase in enzyme activity. These findings show a selective inhibition of phenylephrine activation of phospholipase A2 by either the chelation of intracellular calcium with quin2 or by the calcium antagonist TMB-8 and suggest an essential role for intracellular calcium in alpha adrenergic stimulation of enzyme activity. However, because phenylephrine still stimulates enzyme activity in cells rendered permeable with digitonin, we suggest that the action of phenylephrine cannot be attributed solely to changes in intracellular calcium.

摘要

将棕色脂肪细胞暴露于α-1肾上腺素能受体激动剂去氧肾上腺素中,会激活一种磷脂酶A2,该酶可释放花生四烯酸。由于磷脂酶A2的受体激活需要钙,因此进行了实验以更精确地确定钙在酶活性调节中所起的作用。在本研究中,脂肪细胞被加载了荧光钙螯合剂喹啉2,以缓冲细胞内钙并阻断受体刺激引起的其浓度变化。当加载喹啉2的脂肪细胞在含有0.10 mM钙的缓冲液中孵育时,去氧肾上腺素刺激花生四烯酸释放的能力会严重降低。在细胞内喹啉2浓度为6.6 mM时,刺激的花生四烯酸释放被抑制超过50%,而在13 mM时则被完全阻断。相比之下,去氧肾上腺素对肌醇磷酸积累的刺激不受喹啉2的影响。喹啉2也不影响对外源磷脂酶C、A23187或福斯高林的反应中花生四烯酸的释放。细胞内钙拮抗剂TMB-8也抑制去氧肾上腺素对花生四烯酸释放的刺激,这种作用可被离子霉素逆转。通过用洋地黄皂苷使细胞通透并引入高钙浓度,基础磷脂酶A2活性增加,但去氧肾上腺素仍会导致酶活性进一步增加。这些发现表明,通过用喹啉2螯合细胞内钙或通过钙拮抗剂TMB-8,可选择性抑制去氧肾上腺素对磷脂酶A2的激活,并提示细胞内钙在α肾上腺素能刺激酶活性中起重要作用。然而,由于去氧肾上腺素仍能刺激用洋地黄皂苷使细胞通透后的酶活性,我们认为去氧肾上腺素的作用不能仅仅归因于细胞内钙的变化。

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