Kang Dae-Hwan, Han Myoung-Eun, Song Moo-Ho, Lee Young-Suk, Kim Eun-Hee, Kim Hyun-Jung, Kim Gwang-Ha, Kim Dong-Heon, Yoon Sik, Baek Sun-Yong, Kim Bong-Seon, Kim Jae-Bong, Oh Sae-Ock
Department of Internal Medicine, School of Medicine, Pusan National University, Beomeo-Ri, Yangsan, South Korea.
J Gastroenterol. 2009;44(5):372-9. doi: 10.1007/s00535-009-0006-1. Epub 2009 Mar 17.
Hedgehog signaling plays critical roles during embryonic development. It is also involved in tissue regeneration and carcinogenesis in various adult tissues. Moreover, it regulates the maintenance of cancer stem cells and adult stem cells. Although hedgehog signaling is important in gastric carcinogenesis, its role in gastric regeneration has not been previously examined. In the present study, we evaluated the expression and roles of hedgehog signaling during gastric regeneration.
Gastric ulcers were induced by serosal application of an acetic acid solution in mice. Sham-operated mice served as controls. The proliferation of gastric progenitor cells was studied using bromodeoxyuridine (BrdU). The expression of hedgehog signaling molecules and the differentiation of gastric progenitor cells were examined by immunohistochemical staining and Western blotting.
One day after the induction of gastric ulcer, the proliferation of gastric progenitor cells increased; however, the expression of hedgehog signaling molecules, including sonic hedgehog (Shh), Indian hedgehog (Ihh), desert hedgehog (Dhh), and patched (Ptch1) decreased at the ulcer margin. From 5 days after the induction of gastric ulcer, newly generated gastric glands and their differentiation were observed at the ulcer margin. The expression of hedgehog signaling molecules gradually increased in the newly generated gastric glands of the ulcer margin. Cyclopamine, a specific inhibitor of hedgehog signaling, significantly inhibited the differentiation of mucous cells and parietal cells during the gastric regeneration process.
The above results suggest that hedgehog signaling is involved in the differentiation of gastric progenitor cells during the gastric ulcer repair process.
刺猬信号通路在胚胎发育过程中发挥着关键作用。它还参与各种成年组织的组织再生和癌变过程。此外,它调节癌症干细胞和成年干细胞的维持。尽管刺猬信号通路在胃癌发生中很重要,但其在胃再生中的作用此前尚未得到研究。在本研究中,我们评估了刺猬信号通路在胃再生过程中的表达及作用。
通过在小鼠浆膜上应用醋酸溶液诱导胃溃疡。假手术小鼠作为对照。使用溴脱氧尿苷(BrdU)研究胃祖细胞的增殖。通过免疫组织化学染色和蛋白质印迹法检测刺猬信号分子的表达以及胃祖细胞的分化情况。
胃溃疡诱导后一天,胃祖细胞的增殖增加;然而,刺猬信号分子的表达,包括音猬因子(Shh)、印度刺猬因子(Ihh)、沙漠刺猬因子(Dhh)和 patched(Ptch1)在溃疡边缘处降低。胃溃疡诱导后5天起,在溃疡边缘观察到新生成的胃腺及其分化。刺猬信号分子的表达在溃疡边缘新生成的胃腺中逐渐增加。环杷明,一种刺猬信号通路的特异性抑制剂,在胃再生过程中显著抑制黏液细胞和壁细胞的分化。
上述结果表明刺猬信号通路参与胃溃疡修复过程中胃祖细胞的分化。