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Metabolic substrates alter attachment and differentiated functions of proximal tubule cell culture.
Author(s) -
MingJer Tang,
Richard L. Tannen
Publication year - 1994
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.v4111908
Subject(s) - butyrate , phosphoenolpyruvate carboxykinase , cell culture , alanine , cellular differentiation , cell growth , biology , microbiology and biotechnology , in vitro , biochemistry , sodium butyrate , metabolism , chemistry , medicine , endocrinology , amino acid , enzyme , genetics , fermentation , gene
Proximal tubules cultured in vitro gradually lose their differentiated functions. Because standard culture media lacks several substrates important for renal proximal tubule oxidative metabolism, whether a mixture of substrates including butyrate, alanine, and lactate (BAL) would modify growth and/or differentiated function of proximal tubular cells in culture was examined. Tubules cultured in media supplemented with 2 mM butyrate, alanine, and lactate exhibited enhanced attachment but did not exhibit an altered growth rate. Higher levels of phosphoenolpyruvate carboxykinase and leucine-amino peptidase were sustained, although these activities were still diminished in comparison with that in fresh tubules. Sodium-dependent glucose uptake and dome formation--other reflections of epithelial cell differentiated function--also were enhanced. These studies demonstrate that the substrates used to culture proximal tubules can modify both their attachment and their manifestation of differentiated function in culture.

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