Prinz C, Neumayer N, Mahr S, Classen M, Schepp W
Department of Medicine II, Technical University of Munich, Germany.
Gastroenterology. 1997 Feb;112(2):364-75. doi: 10.1053/gast.1997.v112.pm9024290.
BACKGROUND & AIMS: Histamine-producing enterochromaffin-like (ECL) cells play an integrative role in the regulation of acid secretion. Decreased mucosal histamine concentrations and increased levels of interleukin (IL) 1 beta, IL-6, and IL-8 have been detected in the gastric mucosa inflamed with Helicobacter pylori. The aim of this study was to investigate the response of isolated ECL cells to these cytokines.
Enriched rat gastric ECL cells (85%-95%) were cultured for 2-4 days.
Polymerase chain reaction showed IL-1 and IL-6, but not IL-8 receptors, in ECL cell complementary DNA. Positive receptor staining with biotinylated IL-1 beta corresponded to ECL cell enrichment (92%). IL-6 and IL-8 had no effect on histamine secretion. IL-1 beta (2 U/mL) stimulated basal histamine secretion and nitric oxide production within 60 minutes and cyclic guanosine monophosphate production within 20 minutes. Pretreatment for 20 minutes with IL-1 beta (2 U/mL) attenuated gastrin-stimulated histamine secretion by 40%-50%, reversed by the IL-1 receptor antagonist (10 U/ mL). Pretreatment for 20 minutes with IL-1 beta (2 U/mL) completely inhibited gastrin-stimulated (1 nmol/L) histidine decarboxylase activity. IL-1 beta (2 U/mL, 60 minutes) increased lactate dehydrogenase release to 25% of cell content. Cells pretreated with IL-1 beta did not respond to gastrin after a further 48-hour culture and showed decreased histamine content.
ECL cells appear to express IL-1 receptors. IL-1 beta causes sustained functional impairment of ECL cells in vitro.
产生组胺的肠嗜铬样(ECL)细胞在胃酸分泌调节中起整合作用。在幽门螺杆菌感染的胃黏膜中已检测到黏膜组胺浓度降低以及白细胞介素(IL)-1β、IL-6和IL-8水平升高。本研究的目的是探讨分离的ECL细胞对这些细胞因子的反应。
培养富集的大鼠胃ECL细胞(85%-95%)2-4天。
聚合酶链反应显示ECL细胞互补DNA中有IL-1和IL-6受体,但没有IL-8受体。生物素化的IL-1β阳性受体染色与ECL细胞富集(92%)相对应。IL-6和IL-8对组胺分泌无影响。IL-1β(2 U/mL)在60分钟内刺激基础组胺分泌和一氧化氮产生,在20分钟内刺激环磷酸鸟苷产生。用IL-1β(2 U/mL)预处理20分钟可使胃泌素刺激的组胺分泌减少40%-50%,IL-1受体拮抗剂(10 U/mL)可逆转此作用。用IL-1β(2 U/mL)预处理20分钟可完全抑制胃泌素刺激的(1 nmol/L)组氨酸脱羧酶活性。IL-1β(2 U/mL,60分钟)使乳酸脱氢酶释放增加至细胞内容物的25%。用IL-1β预处理的细胞在进一步培养48小时后对胃泌素无反应,且组胺含量降低。
ECL细胞似乎表达IL-1受体。IL-1β在体外导致ECL细胞持续的功能损害。