ClC-3 is required for LPA-activated Cl- current activity and fibroblast-to-myofibroblast differentiation

Zhaohong Yin, Yiai Tong, Haiqing Zhu, Mitchell Aaron Watsky

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

To determine the effects of chloride channel 3 (ClC-3) knockdown and overexpression on lysophosphatidic acid (LPA)- and volume-regulated anion channel Cl- currents (ICl,LPA and ICl,VRAC, respectively), cell differentiation, and cell volume regulation, a short hairpin RNA (shRNA) expression system based on a mouse U6 promoter was used to knock down ClC-3 in human corneal keratocytes and human fetal lung fibroblasts. ClC-3 overexpression was achieved by electroporating full-length ClC-3, within a pcDNA3.1 vector, into these two cell lines. RT-PCR and Western blot analysis were used to detect ClC-3 mRNA and protein levels. Whole cell perforated patch-clamp recording was used to measure ICl,LPA and I Cl,VRAC currents, and fluorescence-activated cell sorting analysis was used to measure cell volume regulation. ClC-3 knockdown significantly decreased ICl,LPA and ICl,VRAC activity in the presence of transforming growth factor-β1 (TGF-β1) compared with controls, whereas ClC-3 overexpression resulted in increased I Cl,LPA activity in the absence of TGF-β1. ClC-3 knockdown also resulted in a reduction of α-smooth muscle actin (α-SMA) protein levels in the presence of TGF-β1, whereas ClC-3 overexpression increased α-SMA protein expression in the absence of TGF-β1. In addition, keratocytes transfected with ClC-3 shRNA had a significantly blunted regulatory volume decrease response following hyposmotic stimulation compared with controls. These data confirm that ClC-3 is important in VRAC function and cell volume regulation, is associated with the ICl,LPA current activity, and participates in the fibroblast-to-myofibroblast transition.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Cell Physiology
Volume294
Issue number2
DOIs
StatePublished - Feb 1 2008
Externally publishedYes

Fingerprint

Myofibroblasts
Fibroblasts
Transforming Growth Factors
Cell Size
Small Interfering RNA
lysophosphatidic acid
ClC-3 channel
Corneal Keratocytes
Cells
Proteins
Muscle Proteins
Clamping devices
Sorting
Anions
Smooth Muscle
Muscle
Actins
Cell Differentiation
Flow Cytometry
Western Blotting

Keywords

  • Chloride channel-3
  • Cornea
  • Keratocyte
  • Lung
  • Lysophosphatidic acid

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Cell Biology
  • Physiology

Cite this

ClC-3 is required for LPA-activated Cl- current activity and fibroblast-to-myofibroblast differentiation. / Yin, Zhaohong; Tong, Yiai; Zhu, Haiqing; Watsky, Mitchell Aaron.

In: American Journal of Physiology - Cell Physiology, Vol. 294, No. 2, 01.02.2008.

Research output: Contribution to journalArticle

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