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G(o)2和Gi3蛋白介导生长抑素对绵羊垂体生长激素细胞中膜Ca2+和K+电流的作用。

G(o)2 and Gi3 proteins mediate the action of somatostatin on membrane Ca2+ and K+ currents in ovine pituitary somatotrophs.

作者信息

Chen C

机构信息

Prince Henry's Institute of Medical Research, Monash Medical Center, Clayton, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1997 Aug;24(8):639-45. doi: 10.1111/j.1440-1681.1997.tb02105.x.

DOI:10.1111/j.1440-1681.1997.tb02105.x
PMID:9269541
Abstract
  1. Growth hormone (GH) secretion from the anterior pituitary gland is mainly regulated by hypothalamic GH-releasing hormone (GHRH) and somatostatin (SRIF). Somatostatin reduces both spontaneous and GHRH-stimulated GH secretion. 2. Exocytosis of GH is mainly determined by the intracellular free Ca2+ concentration ([Ca2+]i), which is regulated by the influx of Ca2+ via membrane Ca2+ channels. Somatostatin reduces the influx of Ca2+ through two separate mechanisms, namely a direct action on Ca2+ channels and an indirect action on membrane potentials through the activation of K+ channels. 3. In the present experiments, somatotroph-enriched cells were obtained from the ovine pituitary gland by means of collagenase dissociation and Percoll-gradient centrifugation. Further identification was based on the effect of SRIF (10 nmol/L) on Ca2+ or K+ currents. 4. A significant reduction in Ca2+ currents and an increase in K+ currents was obtained in response to local application of SRIF (10 nmol/L), but vehicle application had no effect. The responses of Ca2+ and K+ currents to SRIF were reversible after removal of SRIF. 5. Dialysis of GTP-gamma-s (200 mumol/L) abolished the recovery phase of K+ current response to SRIF after its removal, whereas GDP-beta-s (200 mumol/L) totally blocked the response. Pretreatment of the cells with pertussis toxin (100 nmol/L) overnight abolished the Ca2+ current response to SRIF. 6. Intracellular dialysis of antibodies to alpha o, alpha i1-3, alpha i1-2 and alpha i3 subunits of the G-proteins into cells via whole-cell patch-clamp pipettes was confirmed by immunofluorescent staining of the antibodies. 7. Dialysis of anti-alpha i1-3 or anti-alpha i3 antibodies significantly attenuated the increase in the K+ current in response to 10 nmol/L SRIF, whereas neither anti-alpha o nor anti-alpha i1-2 antibodies diminished the effect of SRIF on the K+ current. 8. Dialysis of anti-alpha o antibodies significantly attenuated the reduction in the Ca2+ current that was obtained upon application of 10 nmol/L SRIF. Neither anti-alpha i1-2 nor anti-alpha i3 antibody dialysis diminished the effect of SRIF on the Ca2+ current. 9. Dialysis of the alpha o common antisense oligonucleotides (ASm) but not the alpha i3 AS significantly diminished the inhibitory effect of SRIF on the Ca2+ current. This effect of alpha o ASm dialysis occurred at 12 h incubation after dialysis, reaching a maximal level at 48 h and partially recovering at 72 h incubation. Antisense oligonucleotides specific for alpha o1 (alpha o1 AS) or alpha o2 (alpha o2 AS) were dialysed into somatotrophs and only alpha o2 AS significantly attenuated the inhibition of SRIF on the Ca2+ current. 10. It is concluded that the Gi3 protein mediates the effect of SRIF on the K+ current and that the G(o)2 protein mediates the effect of SRIF on the Ca2+ current in primary cultured ovine somatotrophs.
摘要
  1. 垂体前叶分泌的生长激素(GH)主要受下丘脑生长激素释放激素(GHRH)和生长抑素(SRIF)的调节。生长抑素可降低自发的以及GHRH刺激的GH分泌。2. GH的胞吐作用主要由细胞内游离钙离子浓度([Ca2+]i)决定,而[Ca2+]i受钙离子经膜钙离子通道内流的调节。生长抑素通过两种不同机制减少钙离子内流,即直接作用于钙离子通道以及通过激活钾离子通道对膜电位产生间接作用。3. 在本实验中,通过胶原酶解离和 Percoll 梯度离心从羊垂体中获得富含生长激素细胞。进一步的鉴定基于生长抑素(10 nmol/L)对钙离子或钾离子电流的影响。4. 局部应用生长抑素(10 nmol/L)可使钙离子电流显著降低,钾离子电流增加,但应用溶剂则无此效应。去除生长抑素后,钙离子和钾离子电流对生长抑素的反应是可逆的。5. 用GTP-γ-s(200 μmol/L)进行透析可消除去除生长抑素后钾离子电流对其反应的恢复阶段,而GDP-β-s(200 μmol/L)则完全阻断该反应。用百日咳毒素(100 nmol/L)对细胞进行过夜预处理可消除钙离子电流对生长抑素的反应。6. 通过全细胞膜片钳吸管将针对G蛋白αo、αi1 - 3、αi1 - 2和αi3亚基的抗体进行细胞内透析,经抗体的免疫荧光染色得以证实。7. 针对αi1 - 3或αi3抗体进行透析可显著减弱10 nmol/L生长抑素引起的钾离子电流增加,而针对αo或αi1 - 2抗体则不会减弱生长抑素对钾离子电流的作用。8. 针对αo抗体进行透析可显著减弱应用10 nmol/L生长抑素时钙离子电流的降低。针对αi1 - 2和αi3抗体进行透析均不会减弱生长抑素对钙离子电流的作用。9. 针对αo的共同反义寡核苷酸(ASm)而非αi3的反义寡核苷酸进行透析可显著减弱生长抑素对钙离子电流的抑制作用。αo ASm透析的这种作用在透析后孵育12小时出现,48小时达到最大水平,72小时孵育时部分恢复。将针对αo1(αo1 AS)或αo2(αo2 AS)的特异性反义寡核苷酸透析到生长激素细胞中,只有αo2 AS可显著减弱生长抑素对钙离子电流的抑制作用。10. 得出结论:在原代培养的羊生长激素细胞中,Gi3蛋白介导生长抑素对钾离子电流的作用,而G(o)2蛋白介导生长抑素对钙离子电流的作用。

相似文献

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G(o)2 and Gi3 proteins mediate the action of somatostatin on membrane Ca2+ and K+ currents in ovine pituitary somatotrophs.G(o)2和Gi3蛋白介导生长抑素对绵羊垂体生长激素细胞中膜Ca2+和K+电流的作用。
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Gi-3 protein mediates the increase in voltage-gated K+ currents by somatostatin on cultured ovine somatotrophs.Gi-3蛋白介导生长抑素对培养的绵羊生长激素细胞电压门控钾电流的增强作用。
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