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培养的小肠上皮细胞未产生气。

NO chi generation by cultured small intestinal epithelial cells.

作者信息

Dignass A U, Podolsky D K, Rachmilewitz D

机构信息

Gastrointestinal Unit, Boston, USA.

出版信息

Dig Dis Sci. 1995 Sep;40(9):1859-65. doi: 10.1007/BF02208647.

DOI:10.1007/BF02208647
PMID:7555434
Abstract

The effect of cytokines, growth factors, mitogens, and bacterial products on nitric oxide (NO) generation by monolayers of small intestinal epithelial cells-6 (IEC-6) cells was evaluated. Subconfluent IEC-6 cells were maintained in DMEM containing 5% fetal calf serum and after 16-24 hr of incubation, the medium was replaced with fresh medium in the presence or absence of calcium ionophore (CaI), L-NAME, L-NNA, individual growth factors, cytokines, or mitogens. After 72 hr of culture, the media supernatant was collected and NO chi generation was determined. NO synthase activity was determined in sonicated supernatants of IEC-6 cells by [14C] arginine conversion to citrulline. NO chi generation in subconfluent cultures was greater than in fully confluent cultures, suggesting contact inhibition. NO chi generation by IEC-6 cells was significantly increased by CaI and inhibited by L-NAME and L-NNA. LPS, IL-1 beta, IL-2, IL-8, IFN-8, TFN-alpha, EGF, TGF-alpha, bFGF, and PHA significantly increased NO chi generation. NO synthase activity in IEC-6 cells (4.2 +/- 1.7 pmol/min/10(6) cells) was NADPH dependent. These results suggest that stimulation of NO chi generation by intestinal epithelial cells through cytokine bacterial products and mitogens may be one of the mechanisms responsible for their effects in the intestinal tract.

摘要

评估了细胞因子、生长因子、促细胞分裂剂和细菌产物对小肠上皮细胞-6(IEC-6)单层细胞产生一氧化氮(NO)的影响。将未汇合的IEC-6细胞培养于含5%胎牛血清的DMEM中,孵育16 - 24小时后,在存在或不存在钙离子载体(CaI)、L- NAME、L- NNA、单独的生长因子、细胞因子或促细胞分裂剂的情况下,用新鲜培养基替换培养基。培养72小时后,收集培养基上清液并测定NO生成量。通过[14C]精氨酸转化为瓜氨酸来测定IEC-6细胞超声处理上清液中的NO合酶活性。未汇合培养物中的NO生成量大于完全汇合培养物中的,提示接触抑制。CaI可显著增加IEC-6细胞的NO生成量,而L- NAME和L- NNA可抑制其生成。脂多糖(LPS)、白细胞介素-1β(IL-1β)、白细胞介素-2(IL-2)、白细胞介素-8(IL-8)、干扰素-γ(IFN-γ)、肿瘤坏死因子-α(TNF-α)、表皮生长因子(EGF)、转化生长因子-α(TGF-α)、碱性成纤维细胞生长因子(bFGF)和植物血凝素(PHA)可显著增加NO生成量。IEC-6细胞中的NO合酶活性(4.2±1.7 pmol/分钟/10⁶个细胞)依赖于烟酰胺腺嘌呤二核苷酸磷酸(NADPH)。这些结果表明,肠道上皮细胞通过细胞因子、细菌产物和促细胞分裂剂刺激NO生成可能是它们在肠道中发挥作用的机制之一。

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本文引用的文献

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Intestinal epithelial cells contribute to the enhanced generation of platelet activating factor in ulcerative colitis.肠上皮细胞促使溃疡性结肠炎中血小板活化因子的生成增加。
Gut. 1993 May;34(5):665-8. doi: 10.1136/gut.34.5.665.
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Characterization and growth regulation of a rat intrahepatic bile duct epithelial cell line under hormonally defined, serum-free conditions.在激素限定的无血清条件下大鼠肝内胆管上皮细胞系的特性鉴定及生长调控
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Increased expression of an inducible isoform of nitric oxide synthase and the formation of peroxynitrite in colonic mucosa of patients with active ulcerative colitis.活动性溃疡性结肠炎患者结肠黏膜中诱导型一氧化氮合酶异构体表达增加及过氧亚硝酸盐的形成。
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