Literature DB >> 6822573

Polarized amino acid transport by an epithelial cell line of renal origin (LLC-PK1). The apical systems.

C A Rabito, M V Karish.   

Abstract

The transport of D-aspartate has been studied in an epithelial cell line from a pig kidney. The amino acid is accumulated by LLC-PK1 cells without evidence of metabolism. The accumulation against a concentration gradient occurs through a mechanism with several features of a carrier-mediated process. The influx may be accounted for by a saturable Na+-dependent and nonsaturable Na+-independent process. The presence of Na+ in the incubation medium increases Vmax without affecting Km. A number of differences in the apparent affinities and specifities allows one to differentiate between this and the acidic amino acid transport system from other tissues. Polarized uptake from either side of the monolayers indicates that the acidic amino acid transport system is preferentially located in the apical membrane of the cultured renal cells. The apical localization of this system clearly contrasts with the basolateral localization of the other three neutral amino acid transport systems reported previously, indicating a high degree of cell polarization. The present study shows a close similarity between the Na+-dependent acidic amino acid transport system in LLC-PK1 cells and the system present in the apical membrane of the proximal tubular cells.

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Year:  1983        PMID: 6822573

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  19 in total

1.  Simulation of animal cell metabolism.

Authors:  J P Barford; P J Phillips; C Harbour
Journal:  Cytotechnology       Date:  1992       Impact factor: 2.058

2.  The polarized expression of Na+,K+-ATPase in epithelia depends on the association between beta-subunits located in neighboring cells.

Authors:  Liora Shoshani; Rubén G Contreras; María L Roldán; Jacqueline Moreno; Amparo Lázaro; María S Balda; Karl Matter; Marcelino Cereijido
Journal:  Mol Biol Cell       Date:  2004-12-22       Impact factor: 4.138

3.  Measurements of intracellular pH in single LLC-PK1 cells: recovery from an acid load via basolateral Na+/H+ exchange.

Authors:  M H Montrose; T Friedrich; H Murer
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

4.  Electrogenic transport of neutral and dibasic amino acids in a cultured opossum kidney cell line (OK).

Authors:  J S Schwegler; A Heuner; S Silbernagl
Journal:  Pflugers Arch       Date:  1989-09       Impact factor: 3.657

5.  Regulation of intracellular pH in LLC-PK1 cells by Na+/H+ exchange.

Authors:  M H Montrose; H Murer
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

6.  Effects of attachment substrates on the growth and differentiation of LLC-PK1 cells.

Authors:  T K Ip; P M Galletti; P Aebischer
Journal:  In Vitro Cell Dev Biol       Date:  1990-02

7.  Pharmacologically different Na/H antiporters on the apical and basolateral surfaces of cultured porcine kidney cells (LLC-PK1).

Authors:  J G Haggerty; N Agarwal; R F Reilly; E A Adelberg; C W Slayman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

8.  Differentiated properties characteristic of renal proximal epithelium in a cell line derived from a normal monkey kidney (JTC-12).

Authors:  Y Takuwa; E Ogata
Journal:  In Vitro Cell Dev Biol       Date:  1985-08

9.  Decreased cellular toxicity of neomycin in a clonal cell line isolated from LLC-PK1.

Authors:  R Hori; M Okuda; Y Ohishi; M Yasuhara; K Inui; M Takano
Journal:  Pharm Res       Date:  1993-04       Impact factor: 4.200

10.  Polarized nature of taurine transport in LLC-PK1 and MDCK cells: Further characterization of divergent transport models.

Authors:  D P Jones; R W Chesney
Journal:  Amino Acids       Date:  1993-10       Impact factor: 3.520

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