Nakano O, Sakamoto C, Konda Y, Matsuda K, Matozaki T, Nishisaki H, Wada K, Suzuki T, Uchida T, Nagao M
Second Department of Internal Medicine, Kobe University School of Medicine.
Nihon Shokakibyo Gakkai Zasshi. 1993 Jan;90(1):9-15.
To understand the mechanism by which prostaglandins (PGs) preserve gastric mucosal integrity, we established a primary cultured monolayer of guinea pig gastric mucous cells, and by using this culture system, we studied whether endogenously released PGE2 could influence the proliferation of the mucous cells. By the histochemical and morphological analysis at 24h of the culture periods, the cells were recognized to contain PAS-positive mucous granules with only 3% of them being parietal cells. Although the cells which were simultaneously labeled with [3H] arachidonic acid in 0.5% serum-containing medium synthesized and released radiolabeled PGE2, PGI2 and PGA2, the release of PGE2 was more markedly observed and was partially dependent upon arachidonic acid added to the culture medium. By radioimmunoassay of the culture media, the mucous cells were found to release PGE2 in a time-dependent manner in response to 10% serum. Pretreatment of the cells with 10(-4)M indomethacin not only inhibited PGE2 release but also inhibited increase in cell number. However, the addition of PGE2 dose-dependently restored the indomethacin-induced inhibition of cell growth with the maximal increase almost to the control level at 10(-6)M PGE2. These results suggest that PGE2 endogenously released from the cells may exert a proliferative effect on gastric mucous cells.
为了解前列腺素(PGs)维持胃黏膜完整性的机制,我们建立了豚鼠胃黏液细胞原代培养单层,并利用该培养系统研究内源性释放的前列腺素E2(PGE2)是否会影响黏液细胞的增殖。通过培养24小时后的组织化学和形态学分析,发现细胞含有过碘酸雪夫反应(PAS)阳性黏液颗粒,其中仅3%为壁细胞。虽然在含0.5%血清的培养基中同时用[3H]花生四烯酸标记的细胞合成并释放了放射性标记的PGE2、前列环素(PGI2)和前列地酸(PGA2),但PGE2的释放更为明显,且部分依赖于添加到培养基中的花生四烯酸。通过对培养基进行放射免疫测定,发现黏液细胞在10%血清刺激下以时间依赖性方式释放PGE2。用10^(-4)M吲哚美辛预处理细胞不仅抑制了PGE2的释放,还抑制了细胞数量的增加。然而,添加PGE2剂量依赖性地恢复了吲哚美辛诱导的细胞生长抑制,在10^(-6)M PGE2时最大增加几乎恢复到对照水平。这些结果表明,细胞内源性释放的PGE2可能对胃黏液细胞发挥增殖作用。