Literature DB >> 1977732

Differences in enzymatic and mechanical isolated rabbit renal proximal tubules: comparison in long-term incubation.

D P Rodeheaver1, M D Aleo, R G Schnellmann.   

Abstract

Suspensions of renal proximal tubules (RPT) are the in vitro model for many biochemical and physiologic investigations. Inasmuch as there are numerous procedures for tubule isolation and the more commonly used enzymatic procedures may disrupt the basement membrane, there is a need for information comparing the influence of various isolation methods on RPT viability and function in long-term suspension. Rabbit RPT isolated a) enzymatically (ENZ) by in vitro collagenase digestion and Percoll size and density purification, and b) mechanically (MECH) by in vitro iron oxide perfusion and purification by sieving and magnetic removal of glomeruli were compared for viability, morphology, and functional stability during long-term suspension. RPT isolated by ENZ and MECH methods had excellent viability (less than 15% lactate dehydrogenase release), limited lipid peroxidation (less than 0.2 nmol MDA.mg protein-1), and stable nystatin-stimulated oxygen consumption (QO2) (38 and 36 nmol O2.mg protein-1.min-1) throughout 24 h of incubation. Basal QO2 was higher in ENZ than MECH tubules (27 and 19 nmol O2.mg protein-1.min-1, respectively), and was unchanged over 24 h in each preparation. The higher basal QO2 in ENZ tubules was ouabain-sensitive, suggesting an increased rate of Na+,K(+)-ATPase activity in these tubules. Total glutathione content (oxidized + reduced) in ENZ and MECH tubules increased over the 24-h incubation from 8 to 18 nmol.mg protein-1. gamma-Glutamyltranspeptidase (GGT) activity of the RPT homogenates was equivalent in both preparations and stable over time. The ratio of suspension GGT activity to homogenate GGT activity doubled (0.4 to 0.8) during the incubation period. MECH tubules retained their tubule structure during 24 h of incubation whereas the ENZ tubules had a striking loss of tubular morphology over time. These results show that ENZ- and MECH-isolated renal proximal tubule suspensions exhibit similar biochemical properties in long-term incubations but differ in ouabain-sensitive QO2 and the retention of tubular morphology. The loss of tubular morphology and the increase in the rate of Na+,K(+)-ATPase activity in ENZ tubules may be secondary to the disruption of the tubular basement membrane.

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Year:  1990        PMID: 1977732     DOI: 10.1007/bf02624615

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  24 in total

1.  Cellular toxicity of bromobenzene and bromobenzene metabolites to rabbit proximal tubules: the role and mechanism of 2-bromohydroquinone.

Authors:  R G Schnellmann; L J Mandel
Journal:  J Pharmacol Exp Ther       Date:  1986-05       Impact factor: 4.030

2.  Primary cultures of rabbit renal proximal tubule cells: I. Growth and biochemical characteristics.

Authors:  M D Aleo; M L Taub; P A Nickerson; P J Kostyniak
Journal:  In Vitro Cell Dev Biol       Date:  1989-09

3.  Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine.

Authors:  O W Griffith
Journal:  Anal Biochem       Date:  1980-07-15       Impact factor: 3.365

4.  Improved separation method for rat proximal and distal renal tubules.

Authors:  F A Gesek; D W Wolff; J W Strandhoy
Journal:  Am J Physiol       Date:  1987-08

5.  Isolation of a pure suspension of rat proximal tubules.

Authors:  P Vinay; A Gougoux; G Lemieux
Journal:  Am J Physiol       Date:  1981-10

6.  Effect of halogenated vinyl cysteine conjugates on renal tubular active transport.

Authors:  C D Hassall; A J Gandolfi; K Brendel
Journal:  Toxicology       Date:  1983 Mar-Apr       Impact factor: 4.221

7.  A mechanism of S-(1,2,3,4,4-pentachloro-1,3-butadienyl)-L-cysteine toxicity to rabbit renal proximal tubules.

Authors:  R G Schnellmann; E A Lock; L J Mandel
Journal:  Toxicol Appl Pharmacol       Date:  1987-09-30       Impact factor: 4.219

8.  Cytoprotective effects of glycine and glutathione against hypoxic injury to renal tubules.

Authors:  J M Weinberg; J A Davis; M Abarzua; T Rajan
Journal:  J Clin Invest       Date:  1987-11       Impact factor: 14.808

9.  Multiple effects of presumed glutathione depletors on rabbit proximal tubules.

Authors:  R G Schnellmann; L J Mandel
Journal:  Kidney Int       Date:  1986-04       Impact factor: 10.612

10.  Characterization of primary rabbit kidney cultures that express proximal tubule functions in a hormonally defined medium.

Authors:  S D Chung; N Alavi; D Livingston; S Hiller; M Taub
Journal:  J Cell Biol       Date:  1982-10       Impact factor: 10.539

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  5 in total

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Authors:  Zabeena P Shaik; E Kim Fifer; Grazyna Nowak
Journal:  Am J Physiol Renal Physiol       Date:  2006-08-29

2.  Decreasing glycolysis increases sensitivity to mitochondrial inhibition in primary cultures of renal proximal tubule cells.

Authors:  R D Griner; R G Schnellmann
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-01       Impact factor: 2.416

3.  Growth of human renal cortical tissue on collagen gel.

Authors:  S G Chang; K Tóth; J D Black; H K Slocum; S D Perrapato; R P Huben; Y M Rustum
Journal:  In Vitro Cell Dev Biol       Date:  1992-02

4.  The role of short chain fatty acid substrates in aerobic and glycolytic metabolism in primary cultures of renal proximal tubule cells.

Authors:  R D Griner; M D Aleo; R G Schnellmann
Journal:  In Vitro Cell Dev Biol Anim       Date:  1993-08       Impact factor: 2.416

5.  Effect of acute acid-base disturbances on ErbB1/2 tyrosine phosphorylation in rabbit renal proximal tubules.

Authors:  Lara A Skelton; Walter F Boron
Journal:  Am J Physiol Renal Physiol       Date:  2013-10-16
  5 in total

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