pCLCA1 becomes a cAMP-dependent chloride conductance mediator in Caco-2 cells

Biochem Biophys Res Commun. 2002 Nov 8;298(4):531-6. doi: 10.1016/s0006-291x(02)02498-1.

Abstract

Members of the CLCA protein family are expressed in airway and intestinal epithelium, where they may participate in secretory activity as mediators of chloride conductance. A calcium-dependent chloride conductance has been observed upon expression of CLCA proteins in non-epithelial cell lines. The pCLCA1 gene, cloned in our laboratory, codes for a product containing a unique A-kinase consensus acceptor site not found in other CLCA proteins. Calcium-dependent, but not cAMP-dependent, chloride conductance increased when pCLCA1 was expressed in NIH/3T3 fibroblasts. We transfected the Caco-2 human colon carcinoma cell line with pCLCA1 to investigate the regulation of CLCA-associated chloride conductance in this differentiated epithelial cell line. Expression of pCLCA1 in the Caco-2 cell line enhanced cAMP-responsive 36Cl efflux, short circuit current, and whole cell chloride current in these cells. This cAMP-dependent chloride conductance was localized to the apical membrane of polarized Caco-2 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Caco-2 Cells
  • Chloride Channels / physiology*
  • Chlorides / physiology*
  • Cyclic AMP / physiology*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • DNA Primers
  • Humans
  • Patch-Clamp Techniques
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • CFTR protein, human
  • CLCA1 protein, human
  • Chloride Channels
  • Chlorides
  • DNA Primers
  • RNA, Messenger
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Cyclic AMP