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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The effect of the angiotensin II (AT1A) receptor stably transfected into human neuroblastoma SH-SY5Y cells on noradrenaline release and changes in intracellular calcium.
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The effect of the angiotensin II (AT1A) receptor stably transfected into human neuroblastoma SH-SY5Y cells on noradrenaline release and changes in intracellular calcium.

机译:血管紧张素II(AT1A)受体稳定转染到人神经母细胞瘤SH-SY5Y细胞中对去甲肾上腺素释放和细胞内钙变化的影响。

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摘要

A stable cell line expressing the angiotensin II (AII) receptor has been obtained by transfecting the human neuroblastoma SH-SY5Y with the plasmid pCEP4 containing the entire coding region of the rat angiotensin AII receptor AT1A. Angiotensin II (AII; 1-100 nM) evokes the release of [3H]noradrenaline ([3H]NA) in this cell line. Pretreatment with 100 nM 12-O-tetradecanoylphorbol-13-acetate (TPA) enhances the AII-evoked release of [3H]NA approximately two-fold. Removal of extracellular Ca2+ ([Ca2+]o) decreases 100 nM AII-evoked release of [3H]NA by over 50% both in the presence and absence of TPA. AII increases intracellular Ca2+ ([Ca2+]i) in this cell line which is consistent with the AT1A receptor being coupled to phospholipase C. Pretreatment with 100 nM TPA for 8 min attenuated the effect of AII on [Ca2+]i. The effects of AT1A receptor stimulation are therefore regulated differently in this cell line by activation of protein kinase C (PKC). Thus a useful cell line has been obtained from the human neuroblastoma SH-SY5Y in which to study at the molecular level the mechanism(s) by which AII regulates NA release.
机译:通过用包含大鼠血管紧张素AII受体AT1A的整个编码区的质粒pCEP4转染人神经母细胞瘤SH-SY5Y,已经获得了表达血管紧张素II(AII)受体的稳定细胞系。血管紧张素II(AII; 1-100 nM)引起该细胞系中[3H]去甲肾上腺素([3H] NA)的释放。用100 nM 12-O-十四烷酰基phorbol-13-乙酸酯(TPA)进行预处理,可将AII诱发的[3H] NA释放提高约2倍。在存在和不存在TPA的情况下,去除细胞外Ca2 +([Ca2 +] o)会使100 nM AII诱发的[3H] NA释放降低50%以上。 AII增加了该细胞系中的细胞内Ca2 +([Ca2 +] i),这与将AT1A受体与磷脂酶C偶联是一致的。用100 nM TPA预处理8分钟可减弱AII对[Ca2 +] i的作用。因此,通过激活蛋白激酶C(PKC)在该细胞系中对AT1A受体刺激的作用进行了不同的调节。因此,已经从人神经母细胞瘤SH-SY5Y获得了有用的细胞系,其中在分子水平上研究AII调节NA释放的机理。

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