Fujita Akikazu, Takeuchi Tadayoshi, Jun Hanai, Hata Fumiaki
Department of Veterinary Pharmacology, Graduate School of Agriculture and Life Sciences, Osaka Prefecture University, Japan.
J Pharmacol Sci. 2003 May;92(1):35-42. doi: 10.1254/jphs.92.35.
In the present study, we examined the expression and the localization of apamin-sensitive small conductance Ca(2+)-activated K(+) channels (SK channels) in the mouse intestine. SK3-immunoreactivity (IR) was detected in both ileum and colon. Double staining experiments showed that SK3-IR was colocalized with prolyl 4-hydroxylase (PH(alpha))-IR, but not with c-Kit-IR which are markers of fibroblast cells and the interstitial cells of Cajal (ICC), respectively. Although SK3-IR was colocalized with vimentin-IR, which is another marker of ICC, the reactivity of SK3-immunopositive cells was weaker than that of ICC. The SK3-immunopositive cells were similarly present in the intestine of c-Kit mutant mice (W/W(V)), in which ICC were absent, and its wild-type mice. The immuno-electron microscopic analysis indicated that SK3 was localized in the cells that had some similar morphological features to ICC, but obviously different from ICC. The SK3-immunopositive cells had gap junctions with the smooth muscle cells. The gap junctions were smaller than those between ICC and smooth muscle cells. These results indicate expression of SK3 in fibroblast-like cells, but not in ICC, and suggest participation of the cells in the intestinal motility.
在本研究中,我们检测了小鼠肠道中蜂毒明肽敏感的小电导钙激活钾通道(SK通道)的表达及定位。在回肠和结肠中均检测到SK3免疫反应性(IR)。双重染色实验表明,SK3-IR与脯氨酰4-羟化酶(PH(α))-IR共定位,但不与分别作为成纤维细胞和Cajal间质细胞(ICC)标志物的c-Kit-IR共定位。尽管SK3-IR与ICC的另一个标志物波形蛋白-IR共定位,但SK3免疫阳性细胞的反应性比ICC弱。SK3免疫阳性细胞在缺乏ICC的c-Kit突变小鼠(W/W(V))及其野生型小鼠的肠道中均有类似存在。免疫电子显微镜分析表明,SK3定位于一些形态特征与ICC相似但明显不同的细胞中。SK3免疫阳性细胞与平滑肌细胞有缝隙连接。这些缝隙连接比ICC与平滑肌细胞之间的缝隙连接小。这些结果表明SK3在成纤维样细胞中表达,而不在ICC中表达,并提示这些细胞参与肠道运动。