Schepp W, Miederer S E, Ruoff H J
Biochim Biophys Acta. 1984 Jun 19;804(2):192-9. doi: 10.1016/0167-4889(84)90149-6.
Human gastric mucosal cells were isolated from the resected fundic mucosa of peptic ulcer patients. The intracellular content and secretion of intrinsic factor were estimated by binding to cyano[57Co]cobalamin. The content was maximal in the enriched parietal cell fraction which also displayed the highest H+ production as measured by amino[14C] pyrine uptake. Secretagogues evoked full response after 15 min of incubation: pentagastrin (181% of basal secretion), carbachol (208%), histamine (250%) and dibutyryl cyclic adenosine monophosphate (304%). The phosphodiesterase inhibitor isobutylmethylxanthine was slightly more effective even than dibutyryl cAMP. The response to histamine was abolished by ranitidine, indicating activation of adenylate cyclase via histamine H2 receptors, but remained unaffected by atropine, which in turn blocked the carbachol effect, whereas ranitidine was ineffective. The mean formation rate was 8.4 fmol intrinsic factor/10(6) cells per h under basal conditions and 14.3 fmol in response to histamine.
从消化性溃疡患者切除的胃底黏膜中分离出人胃黏膜细胞。通过与氰基[57Co]钴胺素结合来估计内因子的细胞内含量和分泌量。在富集的壁细胞组分中含量最高,该组分通过氨基[14C]吡啶摄取测量也显示出最高的H+产生量。促分泌剂在孵育15分钟后引起完全反应:五肽胃泌素(基础分泌的181%)、卡巴胆碱(208%)、组胺(250%)和二丁酰环磷酸腺苷(304%)。磷酸二酯酶抑制剂异丁基甲基黄嘌呤甚至比二丁酰环磷酸腺苷更有效。雷尼替丁消除了对组胺的反应,表明通过组胺H2受体激活腺苷酸环化酶,但不受阿托品影响,而阿托品又阻断了卡巴胆碱的作用,而雷尼替丁无效。基础条件下平均生成率为每小时8.4飞摩尔内因子/10(6)个细胞,对组胺反应时为14.3飞摩尔。