Literature DB >> 6951421

The development of serum-free hormone-supplemented media for primary kidney cultures and their use in examining renal functions.

N Taub, D Livingston.   

Abstract

We have demonstrated the primary kidney cultures and defined medium can be used for several purposes. First, primary kidney cultures can be examined in defined medium to evaluate the physiological significance of studies made with established kidney cell lines. Secondly, new kidney epithelial cell culture systems can be developed, using primary cultures and defined medium. The studies presented here have demonstrated several possible approaches towards these ends. First, a hormone-supplemented serum-free medium (Medium K-1) developed for an established dog kidney epithelial cell line (MDCK) was used to grow primary cultures of baby mouse kidney epithelial cells without fibroblast overgrowth. The primary cultures of baby mouse cells not only grew in response to each of the five supplements in Medium K-1, but also possessed several of the differentiated kidney functions observed in the MDCK cell line. Secondly, defined media were developed for primary cultures of rabbit kidney epithelial cells directly. The rabbit cells were shown to require a different set of supplements than MDCK cells to attain optimal growth. Furthermore primary cultures derived from purified rabbit proximal tubules required a different set of supplements than primary cultures derived from unpurified rabbit kidney tissue. These new primary culture systems should prove invaluable in examining renal transport functions in vitro.

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Year:  1981        PMID: 6951421     DOI: 10.1111/j.1749-6632.1981.tb15491.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  10 in total

1.  Supplementary factors required for serum-free culture of rat kidney cells of line NRK-49F.

Authors:  G L Bradshaw; G R Dubes
Journal:  In Vitro       Date:  1983-10

2.  Initiation and characterization of primary mouse kidney epithelial cultures.

Authors:  C L Bell; H S Tenenhouse; C R Scriver
Journal:  In Vitro Cell Dev Biol       Date:  1988-07

3.  Renal fibrosis: collagen composition and assembly regulates epithelial-mesenchymal transdifferentiation.

Authors:  M Zeisberg; G Bonner; Y Maeshima; P Colorado; G A Müller; F Strutz; R Kalluri
Journal:  Am J Pathol       Date:  2001-10       Impact factor: 4.307

4.  Growth factor requirements of organogenesis in serum-free metanephric organ culture.

Authors:  E D Avner; W E Sweeney; N P Piesco; D Ellis
Journal:  In Vitro Cell Dev Biol       Date:  1985-05

5.  Human foetal kidney explants in serum-free organ culture.

Authors:  N Brière
Journal:  Anat Embryol (Berl)       Date:  1987

6.  Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolism.

Authors:  C L Bell; H S Tenenhouse; C R Scriver
Journal:  Am J Hum Genet       Date:  1988-09       Impact factor: 11.025

7.  Characteristics of long-term human epithelial cell cultures derived from normal human fetal kidney.

Authors:  R E Gibson-D'Ambrosio; M Samuel; C C Chang; J E Trosko; S M D'Ambrosio
Journal:  In Vitro Cell Dev Biol       Date:  1987-04

8.  Characterization of glucose transport by cultured rabbit kidney proximal convoluted and proximal straight tubule cells.

Authors:  Pedro L Del Valle; Anna Trifillis; Charles E Ruegg; Andrew S Kane
Journal:  In Vitro Cell Dev Biol Anim       Date:  2002-04       Impact factor: 2.416

9.  Functional characterization of BC039389-GATM and KLK4-KRSP1 chimeric read-through transcripts which are up-regulated in renal cell cancer.

Authors:  Dorothee Pflueger; Christiane Mittmann; Silvia Dehler; Mark A Rubin; Holger Moch; Peter Schraml
Journal:  BMC Genomics       Date:  2015-03-27       Impact factor: 3.969

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

  10 in total

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