Literature DB >> 9021954

Characterization of a swelling-activated anion conductance in homozygous typing cell hepatoma cells.

K Bodily1, Y Wang, R Roman, A Sostman, J G Fitz.   

Abstract

Liver cell volume and intracellular ion concentrations are maintained within a narrow physiologic range by regulated changes in membrane ion permeability. These studies of homozygous HTC hepatoma cells, a model liver cell line, evaluate the relationship between cell volume and membrane ion permeability, and assess the possibility that cell swelling allows the efflux of the intracellular osmolite taurine through the opening of a conductive pathway. Cell swelling induced by exposure to hypotonic solutions (203 mOsm) caused a rapid increase in cell volume, followed by recovery toward basal values. Volume recovery was inhibited by Cl- depletion or by exposure to the putative Cl- channel blocker 5-nitro-2-(3-phenylpropyl-amino) benzoic acid (NPPB) (25 micromol/L). Swelling increased the efflux rates of 36Cl (181% +/- 15%, P < .01) and 125I (310% +/- 21%, P < .01). In whole cell patch clamp recordings, cell swelling induced by 1) exposure to hypotonic solution or 2) intracellular perfusion with hypertonic sucrose-containing solutions activated an anion-selective current which was outwardly rectified and showed time-dependent inactivation at depolarizing potentials. The current density at -80 mV increased proportionally with increases in the transmembrane osmotic gradient from basal values of -1 pA/pF to maximal values of 70 pA/pF with 100 mmol/L sucrose in the pipette. Basal taurine permeability was low, but cell swelling increased the efflux of [1,2-3H]taurine to 1,587% +/- 172% of basal levels (P < .05). Intracellular perfusion with hypertonic solutions activated currents carried by anionic taurine, with an estimated taurine/Cl- permeability ratio of .88 +/- .17 for whole cell currents. These studies demonstrate that the HTC membrane anion permeability is closely coupled to changes in cell volume, and that the recovery from swelling depends upon activation of anion-selective conductance pathways permeable to both Cl- and taurine.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9021954     DOI: 10.1002/hep.510250224

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  8 in total

1.  Evidence for sustained ATP release from liver cells that is not mediated by vesicular exocytosis.

Authors:  Svjetlana Dolovcak; Shar L Waldrop; Feng Xiao; Gordan Kilic
Journal:  Purinergic Signal       Date:  2011-06-01       Impact factor: 3.765

2.  Initiation of purinergic signaling by exocytosis of ATP-containing vesicles in liver epithelium.

Authors:  Andrew P Feranchak; Matthew A Lewis; Charles Kresge; Meghana Sathe; Abhijit Bugde; Kate Luby-Phelps; Peter P Antich; J Gregory Fitz
Journal:  J Biol Chem       Date:  2010-01-13       Impact factor: 5.157

3.  Blocking swelling-activated chloride current inhibits mouse liver cell proliferation.

Authors:  R Wondergem; W Gong; S H Monen; S N Dooley; J L Gonce; T D Conner; M Houser; T W Ecay; K E Ferslew
Journal:  J Physiol       Date:  2001-05-01       Impact factor: 5.182

4.  p38 MAP kinase modulates liver cell volume through inhibition of membrane Na+ permeability.

Authors:  A P Feranchak; T Berl; J Capasso; P A Wojtaszek; J Han; J G Fitz
Journal:  J Clin Invest       Date:  2001-11       Impact factor: 14.808

5.  Inhibition of cellular responses to insulin in a rat liver cell line. A role for PKC in insulin resistance.

Authors:  Livia Puljak; Michael J Pagliassotti; Yuren Wei; Ishtiaq Qadri; Vinay Parameswara; Victoria Esser; J Gregory Fitz; Gordan Kilic
Journal:  J Physiol       Date:  2005-01-13       Impact factor: 5.182

6.  Glucagon activates Ca2+ and Cl- channels in rat hepatocytes.

Authors:  Edoardo C Aromataris; Michael L Roberts; Greg J Barritt; Grigori Y Rychkov
Journal:  J Physiol       Date:  2006-03-31       Impact factor: 5.182

7.  Plasmodium berghei-infection induces volume-regulated anion channel-like activity in human hepatoma cells.

Authors:  Miguel Prudêncio; Elvira T Derbyshire; Catarina A Marques; Sanjeev Krishna; Maria M Mota; Henry M Staines
Journal:  Cell Microbiol       Date:  2009-06-03       Impact factor: 3.715

8.  5-Nitro-2-(3-phenylpropylamino)benzoic acid (NPPB) stimulates cellular ATP release through exocytosis of ATP-enriched vesicles.

Authors:  Svjetlana Dolovcak; Shar L Waldrop; J Gregory Fitz; Gordan Kilic
Journal:  J Biol Chem       Date:  2009-10-06       Impact factor: 5.157

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.