Loss of functional endothelial connexin40 results in exercise-induced hypertension in mice

Susan K. Morton, Daniel J. Chaston, Lauren Howitt, Jillian Heisler, Bruce J Nicholson, Stephen Fairweather, Stefan Bröer, Anthony W. Ashton, Klaus I. Matthaei, Caryl E. Hill

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Supplemental Digital Content is available in the text. During activity, coordinated vasodilation of microcirculatory networks with upstream supply vessels increases blood flow to skeletal and cardiac muscles and reduces peripheral resistance. Endothelial dysfunction in humans attenuates activity-dependent vasodilation, resulting in exercise-induced hypertension in otherwise normotensive individuals. Underpinning activity-dependent hyperemia is an ascending vasodilation in which the endothelial gap junction protein, connexin (Cx)40, plays an essential role. Because exercise-induced hypertension is proposed as a forerunner to clinical hypertension, we hypothesized that endothelial disruption of Cx40 function in mice may create an animal model of this condition. To this end, we created mice in which a mutant Cx40T152A was expressed alongside wildtype Cx40 selectively in the endothelium. Expression of the Cx40T152A transgene in Xenopus oocytes and mouse coronary endothelial cells in vitro impaired both electric and chemical conductance and acted as a dominant-negative against wildtype Cx40, Cx43, and Cx45, but not Cx37. Endothelial expression of Cx40T152A in Cx40T152ATg mice attenuated ascending vasodilation, without effect on radial coupling through myoendothelial gap junctions. Using radiotelemetry, Cx40T152ATg mice showed an activity-dependent increase in blood pressure, which was significantly greater than in wildtype mice, but significantly less than in chronically hypertensive, Cx40knockout mice. The increase in heart rate with activity was also greater than in wildtype or Cx40knockout mice. We conclude that the endothelial Cx40T152A mutation attenuates activity-dependent vasodilation, producing a model of exercise-induced hypertension. These data highlight the importance of endothelial coupling through Cx40 in regulating blood pressure during activity.

Original languageEnglish (US)
Pages (from-to)662-669
Number of pages8
JournalHypertension
Volume65
Issue number3
DOIs
StatePublished - Mar 4 2015

Fingerprint

Hypertension
Vasodilation
Blood Pressure
Connexin 43
Connexins
Gap Junctions
Hyperemia
Xenopus
Transgenes
Human Activities
Vascular Resistance
Endothelium
Oocytes
Blood Vessels
Myocardium
Skeletal Muscle
Endothelial Cells
Animal Models
Heart Rate
Mutation

Keywords

  • connexin40
  • endothelium
  • exercise
  • gap junctions
  • hypertension

ASJC Scopus subject areas

  • Internal Medicine
  • Medicine(all)

Cite this

Morton, S. K., Chaston, D. J., Howitt, L., Heisler, J., Nicholson, B. J., Fairweather, S., ... Hill, C. E. (2015). Loss of functional endothelial connexin40 results in exercise-induced hypertension in mice. Hypertension, 65(3), 662-669. https://doi.org/10.1161/HYPERTENSIONAHA.114.04578

Loss of functional endothelial connexin40 results in exercise-induced hypertension in mice. / Morton, Susan K.; Chaston, Daniel J.; Howitt, Lauren; Heisler, Jillian; Nicholson, Bruce J; Fairweather, Stephen; Bröer, Stefan; Ashton, Anthony W.; Matthaei, Klaus I.; Hill, Caryl E.

In: Hypertension, Vol. 65, No. 3, 04.03.2015, p. 662-669.

Research output: Contribution to journalArticle

Morton, SK, Chaston, DJ, Howitt, L, Heisler, J, Nicholson, BJ, Fairweather, S, Bröer, S, Ashton, AW, Matthaei, KI & Hill, CE 2015, 'Loss of functional endothelial connexin40 results in exercise-induced hypertension in mice', Hypertension, vol. 65, no. 3, pp. 662-669. https://doi.org/10.1161/HYPERTENSIONAHA.114.04578
Morton, Susan K. ; Chaston, Daniel J. ; Howitt, Lauren ; Heisler, Jillian ; Nicholson, Bruce J ; Fairweather, Stephen ; Bröer, Stefan ; Ashton, Anthony W. ; Matthaei, Klaus I. ; Hill, Caryl E. / Loss of functional endothelial connexin40 results in exercise-induced hypertension in mice. In: Hypertension. 2015 ; Vol. 65, No. 3. pp. 662-669.
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