Literature DB >> 9298248

Liver cell hydration.

D Häussinger1, F Schliess, U Warskulat, S vom Dahl.   

Abstract

Liver cells possess potent mechanisms to maintain their volume, i.e., their hydration state. These volume-regulatory mechanisms, however, are apparently not designed to maintain absolute cell volume constancy; they rather act as dampeners to prevent excessive cell volume deviations, which would otherwise result from cumulative substrate uptake or anisotonic stress. Furthermore, these volume-regulatory mechanisms can even be activated in the resting state by hormones and other stimuli, and by that means cell volume changes are effected secondarily. Thus, liver cell hydration can change within minutes under the influence of aniso-osmolarity, hormones, nutrients, and oxidative stress. Such short-term modulation of cell volume within a narrow range acts as an independent and potent signal which modifies hepatocellular metabolism and gene expression. Accordingly, cell volume homeostasis involves the integration of events that allow cell hydration to play a physiologic role as a regulator of cell function.

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Year:  1997        PMID: 9298248     DOI: 10.1023/a:1007483324138

Source DB:  PubMed          Journal:  Cell Biol Toxicol        ISSN: 0742-2091            Impact factor:   6.691


  4 in total

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Journal:  Radiologe       Date:  2004-12       Impact factor: 0.635

Review 3.  Optimal Fluid Therapy for Traumatic Hemorrhagic Shock.

Authors:  Ronald Chang; John B Holcomb
Journal:  Crit Care Clin       Date:  2017-01       Impact factor: 3.598

4.  Expression of taurine transporter is regulated through the TonE (tonicity-responsive element)/TonEBP (TonE-binding protein) pathway and contributes to cytoprotection in HepG2 cells.

Authors:  Takashi Ito; Yasushi Fujio; Mayo Hirata; Tomoka Takatani; Takahisa Matsuda; Satoko Muraoka; Kyoko Takahashi; Junichi Azuma
Journal:  Biochem J       Date:  2004-08-15       Impact factor: 3.857

  4 in total

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