Hypotonic stress influence the membrane potential and alter the proliferation of keratinocytes in vitro

Research output: Article

16 Citations (Scopus)

Abstract

Keratinocyte proliferation and differentiation is strongly influenced by mechanical forces. We investigated the effect of osmotic changes in the development of HaCaT cells in culture using intracellular calcium measurements, electrophysiological recordings and molecular biology techniques. The application of hypotonic stress (174mOsmol/l) caused a sustained hyperpolarization of HaCaT cells from a resting potential of -27±4 to -51±9mV. This change was partially reversible. The surface membrane channels involved in the hyperpolarization were identified as chloride channels due to the lack of response in the absence of the anion. Cells responded with an elevation of intracellular calcium concentration to hypotonic stress, which critically depended on external calcium. The presence of phorbol-12-myristate-13-acetate in the culture medium for 12h augmented the subsequent response to hypotonic stress. A sudden switch from iso- to hypotonic solution increased cell proliferation and suppressed the production of involucrin, filaggrin and transglutaminase, markers of keratinocyte differentiation. It is concluded that sudden mechanical forces increase the proliferation of keratinocytes through alterations in their membrane potential and intracellular calcium concentration. These changes together with additional modifications in channel expression and intracellular signalling mechanisms could underlie the increased proliferation of keratinocytes in hyperproliferative skin diseases.

Original languageEnglish
Pages (from-to)302-310
Number of pages9
JournalExperimental Dermatology
Volume16
Issue number4
DOIs
Publication statusPublished - ápr. 1 2007

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Dermatology

Fingerprint Dive into the research topics of 'Hypotonic stress influence the membrane potential and alter the proliferation of keratinocytes in vitro'. Together they form a unique fingerprint.

  • Cite this