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胰岛素分泌型哺乳动物HIT和RIN细胞系中生长抑素受体与K+ATP通道的G蛋白偶联特性研究

Characterization of the G protein coupling of a somatostatin receptor to the K+ATP channel in insulin-secreting mammalian HIT and RIN cell lines.

作者信息

Ribalet B, Eddlestone G T

机构信息

Department of Physiology, University of California, Los Angeles 90024, USA.

出版信息

J Physiol. 1995 May 15;485 ( Pt 1)(Pt 1):73-86. doi: 10.1113/jphysiol.1995.sp020713.

Abstract
  1. The G protein-mediated coupling of a somatostatin (somatotropin-releasing inhibitory factor; SRIF) receptor to the ATP-dependent K+ channel (K+ATP channel) has been studied in insulin-secreting cells using the patch clamp technique. 2. In excised outside-out patches, the concentration-dependent stimulation of the K+ATP channel by SRIF was biphasic. Stimulation reached a maximum at 15 nM (EC50 = 5.5 nM), then decayed to a minimum at 50 nM and returned to maximum stimulation at 500 nM. 3. In cell-attached patches, bath-applied SRIF caused K+ATP channel stimulation in most experiments. In a few cases, however, SRIF suppressed channel activity, a response that was reversed by addition of dibutyryl cyclic AMP (DBcAMP). Channel stimulation by SRIF or by DBcAMP did not occur in the presence of glucose. 4. In excised inside-out patches, the alpha-subunits of Gi or G(o)-type G proteins stimulated the K+ATP channel (EC50 = 29 and 42 pM, respectively). The K+ATP channel stimulation by alpha i- or alpha o-subunits had no effect on the concentration-dependent inhibition by ATP. 5. In excised inside-out patches, K+ATP channel activity was reduced by inhibitors of protein kinase C (PKC) and stimulated by a PKC activator. The stimulatory effect of PKC was unaffected by the presence of pertussis toxin, but stimulation by exogenous alpha-subunits of the G protein Gi or G(o) was prevented by PKC inhibitors. 6. From these data we deduce that SRIF can affect K+ATP channel activity directly via a membrane-delimited pathway or indirectly via a pathway requiring diffusible messengers. In the former case, alpha i/alpha o may either enhance PLC activity, stimulating PKC and thus inducing K+ATP channel phosphorylation with consequent increase of activity, or channel phosphorylation by PKC may facilitate a direct stimulation of the channel by alpha i/alpha o. In the latter case, an alpha i/alpha o-induced fall in cAMP contributes to reduced PKA-mediated phosphorylation and suppression of channel activity.
摘要
  1. 利用膜片钳技术,在胰岛素分泌细胞中研究了生长抑素(促生长激素释放抑制因子;SRIF)受体与ATP依赖性钾通道(K⁺ATP通道)的G蛋白介导偶联。2. 在切除的外翻膜片中,SRIF对K⁺ATP通道的浓度依赖性刺激呈双相性。刺激在15 nM时达到最大值(EC50 = 5.5 nM),然后在50 nM时降至最小值,并在500 nM时恢复到最大刺激。3. 在细胞贴附膜片中,在大多数实验中,浴加SRIF可引起K⁺ATP通道刺激。然而,在少数情况下,SRIF会抑制通道活性,加入二丁酰环磷腺苷(DBcAMP)可逆转该反应。在有葡萄糖存在时,SRIF或DBcAMP不会引起通道刺激。4. 在切除的内翻膜片中,Gi或G(o)型G蛋白的α亚基刺激K⁺ATP通道(EC50分别为29和42 pM)。αi或αo亚基对K⁺ATP通道的刺激对ATP的浓度依赖性抑制没有影响。5. 在切除的内翻膜片中,蛋白激酶C(PKC)抑制剂可降低K⁺ATP通道活性,PKC激活剂可刺激该通道活性。PKC的刺激作用不受百日咳毒素存在的影响,但G蛋白Gi或G(o)的外源性α亚基的刺激可被PKC抑制剂阻止。6. 根据这些数据,我们推断SRIF可通过膜限定途径直接影响K⁺ATP通道活性,或通过需要可扩散信使的途径间接影响。在前一种情况下,αi/αo可能增强磷脂酶C(PLC)活性,刺激PKC,从而诱导K⁺ATP通道磷酸化,进而增加活性,或者PKC对通道的磷酸化可能促进αi/αo对通道的直接刺激。在后一种情况下,αi/αo诱导的cAMP下降导致蛋白激酶A(PKA)介导的磷酸化减少和通道活性抑制。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa4/1157973/f97365f1a664/jphysiol00318-0086-a.jpg

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