Parnigotto P P, Conconi M T
Interdepartmental Centre for the Study of Keratinocytes: Pharmaceutical and Clinical Applications, University of Padua, Italy.
Ann Anat. 1998 Dec;180(6):511-8. doi: 10.1016/S0940-9602(98)80057-5.
In this work the relationship between the proliferation of bovine corneal epithelial cells and PGE2 has been studied. Our data indicate that PGE2 plays an important role in the growth of corneal epithelial cells. Actually, epithelial cells cultured on a keratocyte feeder-layer and exposed to indomethacin, a cyclooxygenase inhibitor, have shown a decrease in growth rate at drug concentrations which otherwise did not induce a reduction in the viability of the keratocytes as well as in epithelial cells in separate cultures. This effect has been reversed by an exogenous PGE2 addition to the culture media. Moreover, significant increases have been found in the growth of epithelial cells cultured in the presence of keratocytes, with basal medium and with conditioning medium after adding exogenous PGE2 at concentrations equal to or lower than 10(-6) M. Significant decreases in the dimensions of the corneal epithelial cells have been found only when PGE2 has been added to basal and to conditioning medium, suggesting that the autacoid maintains cell dimension and morphology. The appearance of keratins with high molecular weight (54 and 57 kDa) coupled with the tendency to stratification of the cells cultivated with media supplemented with PGE2, indicates that the autacoid could favour cell differentiation. The action of PGE2 on the corneal epithelial cells does not seem to be influenced by the presence of the fibroblasts and their products, since PGE2 has induced increases in cell growth and morphological variations, independent of cultural conditions and therefore also only in the presence of basal medium.
在本研究中,我们对牛角膜上皮细胞增殖与前列腺素E2(PGE2)之间的关系进行了研究。我们的数据表明,PGE2在角膜上皮细胞生长中发挥着重要作用。实际上,在角膜细胞饲养层上培养并暴露于环氧化酶抑制剂吲哚美辛的上皮细胞,在药物浓度下显示出生长速率降低,而该药物浓度在单独培养中并不会导致角膜细胞以及上皮细胞活力下降。向培养基中添加外源性PGE2可逆转这种效应。此外,发现在存在角膜细胞的情况下、在基础培养基中以及添加浓度等于或低于10^(-6) M的外源性PGE2后的条件培养基中培养的上皮细胞生长显著增加。仅当将PGE2添加到基础培养基和条件培养基中时,才发现角膜上皮细胞尺寸显著减小,这表明该自分泌物质维持细胞尺寸和形态。高分子量角蛋白(54和57 kDa)的出现以及用补充有PGE2的培养基培养的细胞分层倾向,表明该自分泌物质可能促进细胞分化。PGE2对角膜上皮细胞的作用似乎不受成纤维细胞及其产物存在的影响,因为PGE2诱导了细胞生长增加和形态变化,与培养条件无关,因此也仅在存在基础培养基的情况下如此。