Functional properties of proximal tubule cell lines derived from transgenic mice harboring L-pyruvate kinase-SV40 (T) antigen hybrid gene

J Cell Sci. 1993 Mar:104 ( Pt 3):705-12. doi: 10.1242/jcs.104.3.705.

Abstract

This study describes the functional characterization of two cell lines derived from the proximal convoluted (PKSV-PCT cells) and proximal straight (PKSV-PR) tubules microdissected out from kidneys of transgenic mice harboring the simian virus 40 (SV40) large T and small t antigens placed under the control of the rat L-type pyruvate kinase (L-PK) 5' regulatory sequence. Both cell lines exhibited cellular cyclic AMP stimulated by parathormone (PTH) and calcitonin (CT) and a sodium-dependent glucose transporter. Uptake of the fluid-phase marker [3H]inulin showed that both cell lines grown on filters exhibited biphasic apical and basolateral endocytic rates. Results from Northern blot analysis indicate that the expression of the T antigen gene (Tag) is dependent on the concentration of D-glucose in the medium and show that the L-PK construct has maintained its capacity for up- or down-regulation by carbohydrates. Replacement of D-glucose by neoglucogenic substrates (lactate, oxaloacetate) blunted the expression of Tag transcripts and induced arrest of cell growth. Compared to cell grown in D-glucose-enriched medium, the hormonal sensitivities to PTH and CT and the sodium-dependent glucose uptake were unchanged whereas quiescent cells exhibited increased hydrolase content. Thus the proximal function has been preserved in these cultured cells derived from tissue-specific targeted oncogenesis in transgenic mice. As the expression of Tag transcripts is controlled by D-glucose, the structural and physiological characteristics of these cell lines can be studied in either quiescent or active growth conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Polyomavirus Transforming / genetics*
  • Calcitonin / pharmacology
  • Cell Division / drug effects
  • Cell Line, Transformed
  • Culture Media
  • Cyclic AMP / metabolism
  • Endocytosis / physiology
  • Epithelial Cells
  • Epithelium / physiology
  • Gene Expression
  • Glucose / metabolism
  • Glucose / pharmacology
  • Kidney Tubules, Proximal / cytology*
  • Kidney Tubules, Proximal / physiology
  • Mice
  • Mice, Transgenic
  • Monosaccharide Transport Proteins / metabolism
  • Parathyroid Hormone / pharmacology
  • Phenotype
  • Pyruvate Kinase / genetics
  • RNA, Messenger / biosynthesis
  • Regulatory Sequences, Nucleic Acid

Substances

  • Antigens, Polyomavirus Transforming
  • Culture Media
  • Monosaccharide Transport Proteins
  • Parathyroid Hormone
  • RNA, Messenger
  • Calcitonin
  • Cyclic AMP
  • Pyruvate Kinase
  • Glucose