Literature DB >> 6317789

Use of cultured epithelia to study transport and its regulation.

J S Handler.   

Abstract

Epithelial cells from a variety of species and organs form polarized epithelia in culture. When epithelia are grown on a porous surface, such as a millipore filter, transport can be studied using adaptations of standard techniques. In the few years in which cultured epithelia have been studied by transport physiologists, most work has been focused on identification and description of the differentiated transport exhibited by cultured epithelia. Epithelia formed by a continuous line of cells derived from pig kidney (LLC-PK1) exhibit sodium-coupled glucose transport similar to that of the proximal tubule and have vasopressin-sensitive adenylate cyclase that has been studied in great detail. Also of interest are epithelia formed by continuous lines of cells derived from amphibian kidney (A6) and from amphibian urinary bladder (TBM). Each line forms epithelia that have high electrical resistance and amiloride-sensitive sodium transport. Transport is stimulated by aldosterone and by cAMP or hormones that raise cell cAMP levels. In LLC-PK1 and in A6 epithelia, transport and the response to hormones can be manipulated by manipulating the culture conditions. Cultured epithelia have also been used to explore the cell biology of epithelia. Most interesting in this regard are studies of the development and maintenance of epithelial cell polarity. This approach should be especially valuable.

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Year:  1983        PMID: 6317789     DOI: 10.1242/jeb.106.1.55

Source DB:  PubMed          Journal:  J Exp Biol        ISSN: 0022-0949            Impact factor:   3.312


  20 in total

1.  Immunomagnetic separation, primary culture, and characterization of cortical thick ascending limb plus distal convoluted tubule cells from mouse kidney.

Authors:  J H Pizzonia; F A Gesek; S M Kennedy; B A Coutermarsh; B J Bacskai; P A Friedman
Journal:  In Vitro Cell Dev Biol       Date:  1991-05

2.  Mechanisms of liquid flux across pulmonary alveolar epithelial cell monolayers.

Authors:  G S Filippatos; W F Hughes; R Qiao; J I Sznajder; B D Uhal
Journal:  In Vitro Cell Dev Biol Anim       Date:  1997-03       Impact factor: 2.416

3.  Role of the Na,K-ATPase beta-subunit in the cellular accumulation and maturation of the enzyme as assessed by glycosylation inhibitors.

Authors:  D Zamofing; B C Rossier; K Geering
Journal:  J Membr Biol       Date:  1988-08       Impact factor: 1.843

4.  Isolation, characterization, and long-term culture of fetal bovine tracheal epithelial cells.

Authors:  B L Schumann; T E Cody; M L Miller; G D Leikauf
Journal:  In Vitro Cell Dev Biol       Date:  1988-03

5.  Uptake of polymyxin B into renal cells.

Authors:  Kamilia Abdelraouf; Kai-Tai Chang; Taijun Yin; Ming Hu; Vincent H Tam
Journal:  Antimicrob Agents Chemother       Date:  2014-04-14       Impact factor: 5.191

6.  Inhibition of Na(+)-pump expression by impairment of protein glycosylation is independent of the reduced sodium entry into the cell.

Authors:  C H Pedemonte
Journal:  J Membr Biol       Date:  1995-10       Impact factor: 1.843

7.  Impedance analysis of MDCK cells measured by electric cell-substrate impedance sensing.

Authors:  C M Lo; C R Keese; I Giaever
Journal:  Biophys J       Date:  1995-12       Impact factor: 4.033

8.  Culture of sweat gland epithelial cells from normal individuals and patients with cystic fibrosis.

Authors:  G Collie; M Buchwald; P Harper; J R Riordan
Journal:  In Vitro Cell Dev Biol       Date:  1985-10

9.  A rapid method for culturing guinea pig gastric mucous cell monolayers.

Authors:  D W Rattner; S Ito; M J Rutten; W Silen
Journal:  In Vitro Cell Dev Biol       Date:  1985-08

10.  Sodium butyrate increases glucose transporter expression in LLC-PK1 cells.

Authors:  M Takano; D B Rhoads; K J Isselbacher
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

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