M Matsuda, M Osafune, M Ishibashi, E Nakano, M Takaha, T Sonoda, A Hiraoka, T Hada, S Watanabe, K Higashino, S Morimoto
{"title":"Morphologic and biochemical characteristics of human kidney cells in vitro.","authors":"M Matsuda, M Osafune, M Ishibashi, E Nakano, M Takaha, T Sonoda, A Hiraoka, T Hada, S Watanabe, K Higashino, S Morimoto","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>In vitro cultivated cells derived from normal human renal cortex were characterized morphologically and biochemically. Although the epithelial monolayer was composed of heterogeneous cells, it included cells with a surface structure similar to microvilli as well as some resembling the desmosome between neighboring cells. Enzymatic studies revealed a marked decrease in alkaline phosphatase activity, and the activity of gamma-glutamyl transpeptidase was also reduced to about one-fifth of that in the original tissue. The electrophoretic mobility of the enzyme was not identical with that of normal kidney or of the novel enzyme in renal neoplastic tissue. Lactate dehydrogenase activity was similar to that of normal kidney tissue but the isozyme pattern was completely inverted. These cells responded to the addition of 10 ng per ml of parathyroid hormone in culture medium and there was a 33 fold increase in intracellular cyclic adenosine monophosphate. Estrogen specific binding protein was not detectable in the monolayer cells. These results clearly indicated that the biologic transformation observed in the cultivated normal cells was not attributable to simple fetalism or dedifferentiation, but was a more complicated process.</p>","PeriodicalId":14519,"journal":{"name":"Investigative urology","volume":"19 2","pages":"104-8"},"PeriodicalIF":0.0000,"publicationDate":"1981-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Investigative urology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In vitro cultivated cells derived from normal human renal cortex were characterized morphologically and biochemically. Although the epithelial monolayer was composed of heterogeneous cells, it included cells with a surface structure similar to microvilli as well as some resembling the desmosome between neighboring cells. Enzymatic studies revealed a marked decrease in alkaline phosphatase activity, and the activity of gamma-glutamyl transpeptidase was also reduced to about one-fifth of that in the original tissue. The electrophoretic mobility of the enzyme was not identical with that of normal kidney or of the novel enzyme in renal neoplastic tissue. Lactate dehydrogenase activity was similar to that of normal kidney tissue but the isozyme pattern was completely inverted. These cells responded to the addition of 10 ng per ml of parathyroid hormone in culture medium and there was a 33 fold increase in intracellular cyclic adenosine monophosphate. Estrogen specific binding protein was not detectable in the monolayer cells. These results clearly indicated that the biologic transformation observed in the cultivated normal cells was not attributable to simple fetalism or dedifferentiation, but was a more complicated process.
对体外培养的正常人肾皮质细胞进行了形态学和生化表征。虽然上皮单层是由异质细胞组成的,但它包括表面结构类似于微绒毛的细胞,以及一些类似于相邻细胞之间的桥粒的细胞。酶学研究表明,碱性磷酸酶活性明显下降,γ -谷氨酰转肽酶活性也下降到原组织的五分之一左右。该酶的电泳迁移率与正常肾脏或肾肿瘤组织中新酶的电泳迁移率不同。乳酸脱氢酶活性与正常肾组织相似,但同工酶模式完全相反。这些细胞对在培养基中添加10 ng / ml甲状旁腺激素有反应,细胞内环磷酸腺苷增加33倍。雌激素特异性结合蛋白未在单层细胞中检测到。这些结果清楚地表明,在培养的正常细胞中观察到的生物转化不是简单的胎化或去分化,而是一个更复杂的过程。