Donley Vicky R, Hiskett Erin K, Kidder Aimee C, Schermerhorn Thomas
Department of Clinical Sciences, Kansas State University, Manhattan, KS 66506-5606, USA.
BMC Vet Res. 2005 Nov 2;1:8. doi: 10.1186/1746-6148-1-8.
Pancreatic beta cells express ATP-sensitive potassium (KATP) channels that are needed for normal insulin secretion and are targets for drugs that modulate insulin secretion. The KATP channel is composed of two subunits: a sulfonylurea receptor (SUR 1) and an inward rectifying potassium channel (Kir6.2). KATP channel activity is influenced by the metabolic state of the cell and initiates the ionic events that precede insulin exocytosis. Although drugs that target the KATP channel have the expected effects on insulin secretion in dogs, little is known about molecular aspects of this potassium channel. To learn more about canine beta cell KATP channels, we studied KATP channel expression by the normal canine pancreas and by insulin-secreting tumors of dogs.
Pancreatic tissue from normal dogs and tumor tissue from three dogs with histologically-confirmed insulinomas was examined for expression of KATP channel subunits (SUR1 and Kir6.2) using RT-PCR. Normal canine pancreas expressed SUR1 and Kir6.2 subunits of the KATP channel. The partial nucleotide sequences for SUR1 and Kir6.2 obtained from the normal pancreas showed a high degree of homology to published sequences for other mammalian species. SUR1 and Kir6.2 expression was observed in each of the three canine insulinomas examined. Comparison of short sequences from insulinomas with those obtained from normal pancreas did not reveal any mutations in either SUR1 or Kir6.2 in any of the insulinomas.
Canine pancreatic KATP channels have the same subunit composition as those found in the endocrine pancreases of humans, rats, and mice, suggesting that the canine channel is regulated in a similar fashion as in other species. SUR1 and Kir6.2 expression was found in the three insulinomas examined indicating that unregulated insulin secretion by these tumors does not result from failure to express one or both KATP channel subunits.
胰腺β细胞表达对ATP敏感的钾(KATP)通道,该通道是正常胰岛素分泌所必需的,并且是调节胰岛素分泌药物的作用靶点。KATP通道由两个亚基组成:磺脲类受体(SUR 1)和内向整流钾通道(Kir6.2)。KATP通道活性受细胞代谢状态影响,并引发胰岛素胞吐作用之前的离子事件。尽管靶向KATP通道的药物对犬类胰岛素分泌有预期效果,但对该钾通道的分子层面了解甚少。为了更多地了解犬β细胞KATP通道,我们研究了正常犬胰腺以及犬胰岛素分泌肿瘤中KATP通道的表达情况。
使用逆转录聚合酶链反应(RT-PCR)检测正常犬的胰腺组织以及三只经组织学确诊为胰岛素瘤的犬的肿瘤组织中KATP通道亚基(SUR1和Kir6.2)的表达。正常犬胰腺表达KATP通道的SUR1和Kir6.2亚基。从正常胰腺获得的SUR1和Kir6.2的部分核苷酸序列与已发表的其他哺乳动物物种的序列具有高度同源性。在所检测的三个犬胰岛素瘤中均观察到SUR1和Kir6.2的表达。将胰岛素瘤的短序列与从正常胰腺获得的序列进行比较,未发现任何一个胰岛素瘤的SUR1或Kir6.2有任何突变。
犬胰腺KATP通道的亚基组成与人类、大鼠和小鼠内分泌胰腺中的相同,这表明犬类通道的调节方式与其他物种相似。在所检测的三个胰岛素瘤中均发现了SUR1和Kir6.2的表达,这表明这些肿瘤不受调控的胰岛素分泌并非由于未能表达一个或两个KATP通道亚基所致。