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由SUR1的一种新型剪接变体赋予的KATP通道功能特性改变。

Altered functional properties of KATP channel conferred by a novel splice variant of SUR1.

作者信息

Sakura H, Trapp S, Liss B, Ashcroft F M

机构信息

University Laboratory of Physiology, Parks Road, Oxford OX1 3PT, UK.

出版信息

J Physiol. 1999 Dec 1;521 Pt 2(Pt 2):337-50. doi: 10.1111/j.1469-7793.1999.00337.x.

Abstract
  1. ATP-sensitive potassium (KATP) channels are composed of pore-forming (Kir6.x) and regulatory sulphonylurea receptor (SURx) subunits. We have isolated a novel SUR variant (SUR1bDelta33) from a hypothalamic cDNA library. This variant lacked exon 33 and introduced a frameshift that produced a truncated protein lacking the second nucleotide binding domain (NBD2). It was expressed at low levels in hypothalamus, midbrain, heart and the insulin-secreting beta-cell line MIN6. 2. We examined the properties of KATP channels composed of Kir6.2 and SUR1bDelta33 by recording macroscopic currents in membrane patches excised from Xenopus oocytes expressing these subunits. We also investigated the effect of truncating SUR1 at either the start (SUR1bT1) or end (SUR1bT2) of exon 33 on KATP channel properties. 3. Kir6.2/SUR1bDelta33 showed an enhanced open probability (Po = 0.6 at -60 mV) and a reduced ATP sensitivity (Ki, 86 microM), when compared with wild-type channels (Po = 0.3; Ki, 22 microM). However, Kir6.2/SUR1bT1 and Kir6.2/SUR1bT2 resembled the wild-type channel in their Po and ATP sensitivity. 4. Neither MgADP, nor the K+ channel opener diazoxide, enhanced Kir6.2/SUR1bDelta33, Kir6.2/SUR1bT1 or Kir6.2/SUR1bT2 currents, consistent with the idea that these agents require an intact NBD2 for their action. Sulphonylureas blocked KATP channels containing any of the three SUR variants, but in excised patches the extent of block was less than that for the wild-type channel. In intact cells, the extent of sulphonylurea block of Kir6.2/SUR1bDelta33 was greater than that in excised patches and was comparable to that found for wild-type channels. 5. Our results demonstrate that NBD2 is not essential for functional expression or sulphonylurea block, but is required for KATP channel activation by K+ channel openers and nucleotides. Some of the unusual properties of Kir6.2/SUR1bDelta33 resemble those reported for the KATP channel of ventromedial hypothalamic (VMH) neurones, but the fact that this mRNA is expressed at low levels in many other tissues makes it less likely that SUR1bDelta33 serves as the SUR subunit for the VMH KATP channel.
摘要
  1. ATP敏感性钾(KATP)通道由形成孔道的(Kir6.x)和调节性磺脲类受体(SURx)亚基组成。我们从下丘脑cDNA文库中分离出一种新型的SUR变体(SUR1bDelta33)。该变体缺少外显子33,并引入了一个移码突变,产生了一种缺少第二个核苷酸结合结构域(NBD2)的截短蛋白。它在下丘脑、中脑、心脏和胰岛素分泌β细胞系MIN6中低水平表达。2. 我们通过记录从表达这些亚基的非洲爪蟾卵母细胞上切除的膜片中的宏观电流,研究了由Kir6.2和SUR1bDelta33组成的KATP通道的特性。我们还研究了在外显子33起始处(SUR1bT1)或末端(SUR1bT2)截短SUR1对KATP通道特性的影响。3. 与野生型通道(Po = 0.3;Ki,22 microM)相比,Kir6.2/SUR1bDelta33表现出更高的开放概率(在-60 mV时Po = 0.6)和更低的ATP敏感性(Ki,86 microM)。然而,Kir6.2/SUR1bT1和Kir6.2/SUR1bT2在开放概率和ATP敏感性方面与野生型通道相似。4. MgADP和钾通道开放剂二氮嗪均未增强Kir6.2/SUR1bDelta33、Kir6.2/SUR1bT1或Kir6.2/SUR1bT2的电流,这与这些药物需要完整的NBD2才能发挥作用的观点一致。磺脲类药物阻断了包含这三种SUR变体中任何一种的KATP通道,但在切除的膜片中,阻断程度小于野生型通道。在完整细胞中,Kir6.2/SUR1bDelta33的磺脲类药物阻断程度大于切除膜片中的阻断程度,且与野生型通道相当。5. 我们的结果表明,NBD2对于功能表达或磺脲类药物阻断不是必需的,但对于钾通道开放剂和核苷酸激活KATP通道是必需的。Kir6.2/SUR1bDelta33的一些异常特性与腹内侧下丘脑(VMH)神经元的KATP通道所报道的特性相似,但该mRNA在许多其他组织中低水平表达这一事实使得SUR1bDelta33作为VMH KATP通道的SUR亚基的可能性较小。

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