{"title":"大鼠肝细胞膜小泡转运磷酸盐的个体发生。","authors":"F K Ghishan, W Dykes","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The present studies were designed to characterize the developmental aspects of Na(+)-dependent phosphate transport, across the hepatocyte basolateral membranes of the suckling and weanling rats. A well validated technique of plasma membrane vesicles (BLMV) was utilized. Phosphate uptake was driven into an osmotically active intravesicular space as evident by a linear relationship between uptake and 1/osm with no binding component y = 0.04 x-0.03, r2 = 0.99 and y = 0.035x + 0.01, r2 = 0.95 in suckling and weanling BLMV's respectively. The presence of inwardly directed Na+ and pH gradient stimulated phosphate uptake in suckling and weanling BLMV's, however, uptake values under Na+ and pH gradients were greater in weanling rats compared to suckling rats. Kinetics of Na(+)-dependent phosphate uptake were 0.14 +/- 0.01 and 0.28 +/- 0.035 at pH 6.1 (P < 0.05) and 0.1 +/- 0.007 and 0.15 +/- 0.03 nmoles/mg protein/10s (P < 0.05) at pH 7.4 in suckling and weanling rats respectively. Km values were not significantly different. Na+ arsenate and phosphonoformonic acid inhibited Na(+)-dependent phosphate uptake, whereas ATP and P-MB (para-chlomercuribenzoic acid) did not effect Na(+)-dependent phosphate uptake. These studies demonstrate for the first time the presence of a specialized transport system for phosphate across the basolateral membranes of the rat liver during development. This transport system exhibit ontogenic characteristics in regard to its transport capacity.</p>","PeriodicalId":15572,"journal":{"name":"Journal of developmental physiology","volume":"19 5","pages":"197-201"},"PeriodicalIF":0.0000,"publicationDate":"1993-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ontogeny of phosphate transport by rat liver plasma membrane vesicles.\",\"authors\":\"F K Ghishan, W Dykes\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The present studies were designed to characterize the developmental aspects of Na(+)-dependent phosphate transport, across the hepatocyte basolateral membranes of the suckling and weanling rats. A well validated technique of plasma membrane vesicles (BLMV) was utilized. Phosphate uptake was driven into an osmotically active intravesicular space as evident by a linear relationship between uptake and 1/osm with no binding component y = 0.04 x-0.03, r2 = 0.99 and y = 0.035x + 0.01, r2 = 0.95 in suckling and weanling BLMV's respectively. The presence of inwardly directed Na+ and pH gradient stimulated phosphate uptake in suckling and weanling BLMV's, however, uptake values under Na+ and pH gradients were greater in weanling rats compared to suckling rats. Kinetics of Na(+)-dependent phosphate uptake were 0.14 +/- 0.01 and 0.28 +/- 0.035 at pH 6.1 (P < 0.05) and 0.1 +/- 0.007 and 0.15 +/- 0.03 nmoles/mg protein/10s (P < 0.05) at pH 7.4 in suckling and weanling rats respectively. Km values were not significantly different. Na+ arsenate and phosphonoformonic acid inhibited Na(+)-dependent phosphate uptake, whereas ATP and P-MB (para-chlomercuribenzoic acid) did not effect Na(+)-dependent phosphate uptake. These studies demonstrate for the first time the presence of a specialized transport system for phosphate across the basolateral membranes of the rat liver during development. This transport system exhibit ontogenic characteristics in regard to its transport capacity.</p>\",\"PeriodicalId\":15572,\"journal\":{\"name\":\"Journal of developmental physiology\",\"volume\":\"19 5\",\"pages\":\"197-201\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of developmental physiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of developmental physiology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Ontogeny of phosphate transport by rat liver plasma membrane vesicles.
The present studies were designed to characterize the developmental aspects of Na(+)-dependent phosphate transport, across the hepatocyte basolateral membranes of the suckling and weanling rats. A well validated technique of plasma membrane vesicles (BLMV) was utilized. Phosphate uptake was driven into an osmotically active intravesicular space as evident by a linear relationship between uptake and 1/osm with no binding component y = 0.04 x-0.03, r2 = 0.99 and y = 0.035x + 0.01, r2 = 0.95 in suckling and weanling BLMV's respectively. The presence of inwardly directed Na+ and pH gradient stimulated phosphate uptake in suckling and weanling BLMV's, however, uptake values under Na+ and pH gradients were greater in weanling rats compared to suckling rats. Kinetics of Na(+)-dependent phosphate uptake were 0.14 +/- 0.01 and 0.28 +/- 0.035 at pH 6.1 (P < 0.05) and 0.1 +/- 0.007 and 0.15 +/- 0.03 nmoles/mg protein/10s (P < 0.05) at pH 7.4 in suckling and weanling rats respectively. Km values were not significantly different. Na+ arsenate and phosphonoformonic acid inhibited Na(+)-dependent phosphate uptake, whereas ATP and P-MB (para-chlomercuribenzoic acid) did not effect Na(+)-dependent phosphate uptake. These studies demonstrate for the first time the presence of a specialized transport system for phosphate across the basolateral membranes of the rat liver during development. This transport system exhibit ontogenic characteristics in regard to its transport capacity.