Chen Duan, Aihara Takeshi, Zhao Chun-Mei, Håkanson Rolf, Okabe Susumu
Dept. of Cancer Research and Molecular Medicine, Norwegian Univ. of Science and Technology, Laboratory Centre, Erling Skjalgssons Gate 1, NO-7006 Trondheim, Norway.
Am J Physiol Gastrointest Liver Physiol. 2006 Oct;291(4):G539-44. doi: 10.1152/ajpgi.00178.2006.
Many physiological functions of the stomach depend on an intact mucosal integrity; function reflects structure and vice versa. Histamine in the stomach is synthesized by histidine decarboxylase (HDC), stored in enterochromaffin-like (ECL) cells, and released in response to gastrin, acting on CCK(2) receptors on the ECL cells. Mobilized ECL cell histamine stimulates histamine H(2) receptors on the parietal cells, resulting in acid secretion. The parietal cells express H(2), M(3), and CCK(2) receptors and somatostatin sst(2) receptors. This review discusses the consequences of disrupting genes that are important for ECL cell histamine release and synthesis (HDC, gastrin, and CCK(2) receptor genes) and genes that are important for "cross-talk" between H(2) receptors and other receptors on the parietal cell (CCK(2), M(3), and sst(2) receptors). Such analysis may provide insight into the functional significance of gastric histamine.
胃的许多生理功能依赖于完整的黏膜完整性;功能反映结构,反之亦然。胃中的组胺由组氨酸脱羧酶(HDC)合成,储存于肠嗜铬样(ECL)细胞中,并在胃泌素的作用下释放,作用于ECL细胞上的CCK(2)受体。被动员的ECL细胞组胺刺激壁细胞上的组胺H(2)受体,导致胃酸分泌。壁细胞表达H(2)、M(3)和CCK(2)受体以及生长抑素sst(2)受体。本综述讨论了破坏对ECL细胞组胺释放和合成重要的基因(HDC、胃泌素和CCK(2)受体基因)以及对壁细胞上H(2)受体与其他受体之间“串扰”重要的基因(CCK(2)、M(3)和sst(2)受体)的后果。此类分析可能有助于深入了解胃组胺的功能意义。