Fibroblast cytoskeletal remodeling induced by tissue stretch involves ATP signaling1. Issue 9 (25th May 2013)

• Record Type: Journal Article
• Authors: Langevin, Helene M.; Fujita, Takumi; Bouffard, Nicole A.; Takano, Takahiro; Koptiuch, Cathryn; Badger, Gary J.; Nedergaard, Maiken
• Is Part Of: Journal of cellular physiology. Volume 228:Issue 9(2013:Sep.)
• Page Start: 1922
• Page End: 1926
• Publication Date: 2013-05-25
• Subjects: Physiology -- Periodicals; Cell physiology -- Periodicals; 571.6
• DOI: 10.1002/jcp.24356
• Languages: English
• ISSNs: 0021-9541

Abstract

Abstract: Fibroblasts in whole areolar connective tissue respond to static stretching of the tissue by expanding and remodeling their cytoskeleton within minutes both ex vivo and in vivo. This study tested the hypothesis that the mechanism of fibroblast expansion in response to tissue stretch involves extracellular ATP signaling. In response to tissue stretch ex vivo, ATP levels in the bath solution increased significantly, and this increase was sustained for 20 min, returning to baseline at 60 min. No increase in ATP was observed in tissue incubated without stretch or tissue stretched in the presence of the Rho kinase inhibitor Y27632. The increase in fibroblast cross sectional area in response to tissue stretch was blocked by both suramin (a purinergic receptor blocker) and apyrase (an enzyme that selectively degrades extracellular ATP). Furthermore, connexin channel blockers (octanol and carbenoxolone), but not VRAC (fluoxetine) or pannexin (probenecid) channel blockers, inhibited fibroblast expansion. Together, these results support a mechanism in which extracellular ATP signaling via connexin hemichannels mediate the active change in fibroblast shape that occurs in response to a static increase in tissue length. J. Cell. Physiol. 228: 1922–1926, 2013. © 2013 Wiley Periodicals, Inc.