Biochemical characterization of renal epithelial cell cultures (LLC-PK1 and MDCK)
- PMID: 3985161
- DOI: 10.1152/ajprenal.1985.248.4.F536
Biochemical characterization of renal epithelial cell cultures (LLC-PK1 and MDCK)
Abstract
The expression of enzymes in LLC-PK1 and MDCK cells was used to study the retention of differentiated properties of the renal epithelial cell lines by a biochemical approach. Activities of marker enzymes, for which intracellular and intranephron localization is known, were determined from crude cell homogenates of LLC-PK1 and MDCK monolayer cultures. The activity patterns of the particular enzymes found were then compared with the in vivo distribution of the enzymes along the rat nephron. LLC-PK1 cells exhibit high activities of apical membrane enzymes when compared with MDCK cells, whereas in the latter high activity of Na-K-ATPase could be detected. The activities of lysosomal enzymes, mitochondrial enzymes, and transaminases were higher in LLC-PK1 than in MDCK cells. Glycolytic enzymes, however, displayed identical activity levels in both the LLC-PK1 and MDCK cells, which may be due to the fact that these are continuous cell lines and to the culture conditions used, since glucose is a major energy source in the culture media.
Similar articles
-
Selective release of apical membrane enzymes from cultured renal epithelia by phosphatidylinositol-specific phospholipase C.Ren Physiol Biochem. 1993 Nov-Dec;16(6):299-310. doi: 10.1159/000173776. Ren Physiol Biochem. 1993. PMID: 7506439
-
Morphological and biochemical changes of LLC-PK1 cells during adaptation to glucose-free culture conditions.Ren Physiol Biochem. 1990 May-Jun;13(3):137-53. doi: 10.1159/000173360. Ren Physiol Biochem. 1990. PMID: 1690907
-
Tyrosine-based membrane protein sorting signals are differentially interpreted by polarized Madin-Darby canine kidney and LLC-PK1 epithelial cells.J Biol Chem. 1998 Oct 9;273(41):26862-9. doi: 10.1074/jbc.273.41.26862. J Biol Chem. 1998. PMID: 9756932
-
Sodium cotransport processes in renal epithelial cell lines.Miner Electrolyte Metab. 1986;12(1):32-41. Miner Electrolyte Metab. 1986. PMID: 2421146 Review.
-
Enzyme distribution along the nephron.Kidney Int. 1984 Aug;26(2):101-11. doi: 10.1038/ki.1984.143. Kidney Int. 1984. PMID: 6094907 Review. No abstract available.
Cited by
-
Measurements of intracellular pH in single LLC-PK1 cells: recovery from an acid load via basolateral Na+/H+ exchange.J Membr Biol. 1987;97(1):63-78. doi: 10.1007/BF01869615. J Membr Biol. 1987. PMID: 3039145
-
Effects of attachment substrates on the growth and differentiation of LLC-PK1 cells.In Vitro Cell Dev Biol. 1990 Feb;26(2):162-8. doi: 10.1007/BF02624108. In Vitro Cell Dev Biol. 1990. PMID: 2312499
-
Pharmacologically different Na/H antiporters on the apical and basolateral surfaces of cultured porcine kidney cells (LLC-PK1).Proc Natl Acad Sci U S A. 1988 Sep;85(18):6797-801. doi: 10.1073/pnas.85.18.6797. Proc Natl Acad Sci U S A. 1988. PMID: 2901105 Free PMC article.
-
An aqueous extract of Ammi visnaga fruits and its constituents khellin and visnagin prevent cell damage caused by oxalate in renal epithelial cells.Phytomedicine. 2010 Jul;17(8-9):653-8. doi: 10.1016/j.phymed.2009.10.011. Epub 2009 Dec 29. Phytomedicine. 2010. PMID: 20036111 Free PMC article.
-
The effect of intracrystalline and surface-bound osteopontin on the degradation and dissolution of calcium oxalate dihydrate crystals in MDCKII cells.Urol Res. 2012 Feb;40(1):1-15. doi: 10.1007/s00240-011-0423-5. Epub 2011 Sep 20. Urol Res. 2012. PMID: 21932131
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources