Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1988 Jul;54(1):187–190. doi: 10.1016/S0006-3495(88)82944-8

Stretch-activated cation channels in human fibroblasts.

L L Stockbridge 1, A S French 1
PMCID: PMC1330329  PMID: 2458140

Abstract

Nonconfluent fibroblasts are relatively depolarized when compared with confluent fibroblasts, and transient hyperpolarizations result from a range of external stimuli as well as internal cellular activities. This electrical activity ceases, along with growth and mitogenic activity, when the cells become confluent. A calcium-activated potassium conductance is thought to be responsible for these hyperpolarizations, but in human fibroblasts the large calcium-activated potassium channel is not stretch-activated. We report here the identification of single stretch-activated cation channels in human fibroblasts, using the cell-attached and inside-out patch clamp techniques. The most prominent channel had a conductance of approximately 60 pS (picoSeimens) in 140 mM potassium and was permeable to potassium and sodium. The channel showed significant adaptation of activity when stretch was maintained over a period of several seconds, but a static component persisted for much longer periods. Higher conductance channels were also observed in a few excised patches.

Full text

PDF
188

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Binggeli R., Weinstein R. C. Membrane potentials and sodium channels: hypotheses for growth regulation and cancer formation based on changes in sodium channels and gap junctions. J Theor Biol. 1986 Dec 21;123(4):377–401. doi: 10.1016/s0022-5193(86)80209-0. [DOI] [PubMed] [Google Scholar]
  2. Brew H., Gray P. T., Mobbs P., Attwell D. Endfeet of retinal glial cells have higher densities of ion channels that mediate K+ buffering. Nature. 1986 Dec 4;324(6096):466–468. doi: 10.1038/324466a0. [DOI] [PubMed] [Google Scholar]
  3. Christensen O. Mediation of cell volume regulation by Ca2+ influx through stretch-activated channels. Nature. 1987 Nov 5;330(6143):66–68. doi: 10.1038/330066a0. [DOI] [PubMed] [Google Scholar]
  4. Colquhoun D., Hawkes A. G. On the stochastic properties of single ion channels. Proc R Soc Lond B Biol Sci. 1981 Mar 6;211(1183):205–235. doi: 10.1098/rspb.1981.0003. [DOI] [PubMed] [Google Scholar]
  5. Cooper K. E., Tang J. M., Rae J. L., Eisenberg R. S. A cation channel in frog lens epithelia responsive to pressure and calcium. J Membr Biol. 1986;93(3):259–269. doi: 10.1007/BF01871180. [DOI] [PubMed] [Google Scholar]
  6. French A. S., Stockbridge L. L. Potassium channels in human and avian fibroblasts. Proc R Soc Lond B Biol Sci. 1988 Jan 22;232(1269):395–412. doi: 10.1098/rspb.1988.0003. [DOI] [PubMed] [Google Scholar]
  7. Guharay F., Sachs F. Stretch-activated single ion channel currents in tissue-cultured embryonic chick skeletal muscle. J Physiol. 1984 Jul;352:685–701. doi: 10.1113/jphysiol.1984.sp015317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hosoi S., Slayman C. L. Membrane voltage, resistance, and channel switching in isolated mouse fibroblasts (L cells): a patch-electrode analysis. J Physiol. 1985 Oct;367:267–290. doi: 10.1113/jphysiol.1985.sp015824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lansman J. B., Hallam T. J., Rink T. J. Single stretch-activated ion channels in vascular endothelial cells as mechanotransducers? 1987 Feb 26-Mar 4Nature. 325(6107):811–813. doi: 10.1038/325811a0. [DOI] [PubMed] [Google Scholar]
  10. Nelson P. G., Peacock J., Minna J. An active electrical response in fibroblasts. J Gen Physiol. 1972 Jul;60(1):58–71. doi: 10.1085/jgp.60.1.58. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Newman E. A. High potassium conductance in astrocyte endfeet. Science. 1986 Jul 25;233(4762):453–454. doi: 10.1126/science.3726539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Okada Y., Tsuchiya W., Yada T., Yano J., Yawo H. Phagocytic activity and hyperpolarizing responses in L-strain mouse fibroblasts. J Physiol. 1981;313:101–119. doi: 10.1113/jphysiol.1981.sp013653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Oliveira-Castro G. M. Ca2+-sensitive K+ channels in phagocytic cell membranes. Cell Calcium. 1983 Dec;4(5-6):475–492. doi: 10.1016/0143-4160(83)90023-4. [DOI] [PubMed] [Google Scholar]
  14. Tsuchiya W., Okada Y., Yano J., Murai A., Miyahara T., Tanaka T. Membrane potential changes associated with pinocytosis of serum lipoproteins in L cells. Exp Cell Res. 1981 Dec;136(2):271–278. doi: 10.1016/0014-4827(81)90005-7. [DOI] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES