Literature DB >> 6911762

Identification of two strains of cultured canine renal epithelial cells (MDCK cells) which display entirely different physiological properties.

G Barker, N L Simmons.   

Abstract

Cultured monolayers of Madin-Derby canine kidney (MDCK) cells grown upon permeable filter supports display many features of in vivo epithelia. Measurements of transmonolayer resistance, open-circuit p.d., dilution and bi-ionic p.d.s have been made of MDCK monolayers mounted in Ussing-type chamber (0.75 cm window radius). Previously reported values of transmonolayer resistance of 100 omega cm2 (Cereijido, Robbins, Dolan, Rotunno & Sabatini, 1978; Misfeldt, Hamamoto & Pitelka, 1976) indicate a 'leaky' epithelium. The major finding of this work is that MDCK monolayers can also display values of transmonolayer resistance similar to 'tight' epithelia (mean value = 4116 omega cm2). The reason for such differences is the existence of separate strains of MDCK cells. High-resistance monolayers originate from cell stocks of sixty serial passages whilst low-resistance monolayers originate from cell stocks of 109 serial passages. Measurements of transmonolayer dilution, and bi-ionic p.d.s together with Na ion tracer fluxes and electron microscope observations of La3+ penetration through the apical tight junctions, substantiate the finding of high-resistance properties in MDCK monolayers and confirm the existence of two separate MDCK cell strains displaying entirely different physiological properties. Differences extend to cellular morphology and cellular volume in the two strains of MDCK cells.

Entities:  

Mesh:

Year:  1981        PMID: 6911762     DOI: 10.1113/expphysiol.1981.sp002529

Source DB:  PubMed          Journal:  Q J Exp Physiol        ISSN: 0144-8757


  30 in total

1.  Stable, polarised, functional expression of Kir1.1b channel protein in Madin-Darby canine kidney cell line.

Authors:  B Ortega; I D Millar; A H Beesley; L Robson; S J White
Journal:  J Physiol       Date:  2000-10-01       Impact factor: 5.182

2.  Paracellular ion channel at the tight junction.

Authors:  Vivian W Tang; Daniel A Goodenough
Journal:  Biophys J       Date:  2003-03       Impact factor: 4.033

3.  The effect of hyperosmotic challenge upon ion transport in cultured renal epithelial layers (MDCK).

Authors:  N L Simmons; D R Tivey
Journal:  Pflugers Arch       Date:  1992-08       Impact factor: 3.657

4.  Autophagy enhances intestinal epithelial tight junction barrier function by targeting claudin-2 protein degradation.

Authors:  Prashant K Nighot; Chien-An Andy Hu; Thomas Y Ma
Journal:  J Biol Chem       Date:  2015-01-23       Impact factor: 5.157

5.  Voltage and Ca2+-activated K+ channel in cultured epithelial cells (MDCK).

Authors:  J J Bolívar; M Cereijido
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

Review 6.  Role of autophagy in the regulation of epithelial cell junctions.

Authors:  Prashant Nighot; Thomas Ma
Journal:  Tissue Barriers       Date:  2016-06-09

Review 7.  Multiorgan Microphysiological Systems for Drug Development: Strategies, Advances, and Challenges.

Authors:  Ying I Wang; Carlos Carmona; James J Hickman; Michael L Shuler
Journal:  Adv Healthc Mater       Date:  2017-12-04       Impact factor: 9.933

8.  Passive transepithelial absorption of thyrotropin-releasing hormone (TRH) via a paracellular route in cultured intestinal and renal epithelial cell lines.

Authors:  D T Thwaites; B H Hirst; N L Simmons
Journal:  Pharm Res       Date:  1993-05       Impact factor: 4.200

9.  The effect of hypo-osmolarity upon transepithelial ion transport in cultured renal epithelial layers (MDCK).

Authors:  N L Simmons
Journal:  Pflugers Arch       Date:  1991-12       Impact factor: 3.657

10.  Protein kinase D-mediated phosphorylation of polycystin-2 (TRPP2) is essential for its effects on cell growth and calcium channel activity.

Authors:  Andrew J Streets; Andrew J Needham; Sharonjit K Gill; Albert C M Ong
Journal:  Mol Biol Cell       Date:  2010-09-29       Impact factor: 4.138

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