Literature DB >> 15348927

Functionality of MDCK kidney tubular cells on flat polymer membranes for biohybrid kidney.

F Fey-Lamprecht1, U Gross, T H Groth, W Albrecht, D Paul, M Fromm, A H Gitter.   

Abstract

The prerequisite for the development of a biohybrid artificial kidney, is a substrate for confluent growth of renal cells forming an epithelial monolayer without any leaks. Conventional cell culture supports cannot be adapted for this purpose, because they lack adequate mechanical properties and thermal stability. From two suitable materials, polysulfone and polyacrylonitrile, two permeable polymeric membranes have been produced that were, according to ISO 10993-5, not cytotoxic. Cloned Madin Darby Canine Kidney (MDCK) cells (an established renal cell line) were cultured on the surface of the plastic materials, and on conventional cell culture supports. With all materials, assays of mitochondrial and lactate dyhydrogenases exhibited similar proliferation and the viability of the MDCK cells. Transmission electron microscopy showed the expression of a normal morphology of kidney tubular cells. Perfect barrier function, consequent on the formation of intercellular junctions in a confluent tight epithelium, was visualized in electron micrographs, and quantified by measurement of the transepithelial resistance. The uniformity of the cells grown was demonstrated in samples by electron microscopy and in the whole epithelium by intravital impedance analysis. It was concluded that polymeric membranes produced from polysulfone or polyacrylonitrile are appropriate substrates in the design of biohybrid kidney devices. Copyright 1998 Kluwer Academic Publishers

Entities:  

Year:  1998        PMID: 15348927     DOI: 10.1023/a:1008994601138

Source DB:  PubMed          Journal:  J Mater Sci Mater Med        ISSN: 0957-4530            Impact factor:   3.896


  8 in total

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Authors:  H P SCHWAN
Journal:  Adv Biol Med Phys       Date:  1957

2.  Ussing chamber for high-frequency transmural impedance analysis of epithelial tissues.

Authors:  A H Gitter; J D Schulzke; D Sorgenfrei; M Fromm
Journal:  J Biochem Biophys Methods       Date:  1997-09-25

3.  Biocompatibility of hemodialysis membranes: a study in healthy subjects.

Authors:  A Gutierrez; A Alvestrand; J Bergström; H Beving; B Lantz; L W Henderson
Journal:  Blood Purif       Date:  1994       Impact factor: 2.614

4.  Characterization of two MDCK-cell subtypes as a model system to study principal cell and intercalated cell properties.

Authors:  M Gekle; S Wünsch; H Oberleithner; S Silbernagl
Journal:  Pflugers Arch       Date:  1994-09       Impact factor: 3.657

Review 5.  Tissue engineering of a bioartificial kidney: a universal donor organ.

Authors:  H D Humes
Journal:  Transplant Proc       Date:  1996-08       Impact factor: 1.066

6.  Monocyte production of transforming growth factor beta in long-term hemodialysis: modulation by hemodialysis membranes.

Authors:  J L Mege; C Capo; R Purgus; M Olmer
Journal:  Am J Kidney Dis       Date:  1996-09       Impact factor: 8.860

Review 7.  Biocompatibility and capability of haemopurification systems: review and future development.

Authors:  K Ota
Journal:  Nephrol Dial Transplant       Date:  1991       Impact factor: 5.992

8.  Protamine reversibly decreases paracellular cation permeability in Necturus gallbladder.

Authors:  M Fromm; C E Palant; C J Bentzel; U Hegel
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

  8 in total

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