Hetero-domain interactions as a mechanism for the regulation of connexin channels

Kathleen Stergiopoulos, José Luis Alvarado, Marta Mastroianni, Jose F Ek Vitorin, Steven M. Taffet, Mario Delmar

Research output: Contribution to journalArticle

113 Citations (Scopus)

Abstract

Previous studies have shown that chemical regulation of connexin43 (Cx43) depends on the presence of the carboxyl terminal (CT) domain. A particle-receptor (or 'ball-and-chain') model has been proposed to explain the mechanism of gating. We tested whether the CT region behaved as a functional domain for other members of the connexin family. The pH sensitivity of wild-type and Ct-truncated connexins was quantified by use of electrophysiological and optical techniques and the Xenopus oocyte system. The CT domain of Cx45 had no role in pH regulation, although a partial role was shown for Cx37 and Cx50. A prominent effect was observed for Cx40 and Cx43. In addition, we found that the CT domain of Cx40 that was expressed as a separate fragment rescued the pH sensitivity of the truncated Cx40 (Cx40tr), which was in agreement with a particle-receptor model. Because Cx40 and Cx43 often colocalize and possibly heteromerize, we tested the pH sensitivity of Cx40tr when coexpressed with the CT domain of Cx43 (hetero- domain interactions). We found that the CT domain of Cx43 enhanced the pH sensitivity of Cx40tr; similarly, the CT domain of Cx40 restored the pH sensitivity of the truncated Cx43. In addition, the CT domain of Cx43 granted insulin sensitivity to the otherwise insulin-insensitive Cx26 or Cx32 channels. These data show that the particle-receptor model is preserved in Cx40 and the regulatory domain of one connexin can specifically interact with a channel formed by another connexin. Hetero-domain interactions could be critical for the regulation of heteromeric channels.

Original languageEnglish (US)
Pages (from-to)1144-1155
Number of pages12
JournalCirculation Research
Volume84
Issue number10
StatePublished - May 28 1999
Externally publishedYes

Fingerprint

Connexin 43
Connexins
Xenopus
Oocytes
Insulin Resistance
Insulin

Keywords

  • Connexin
  • Hetero-domain interaction
  • Insulin
  • pH, regulation
  • Xenopus oocyte

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Stergiopoulos, K., Alvarado, J. L., Mastroianni, M., Ek Vitorin, J. F., Taffet, S. M., & Delmar, M. (1999). Hetero-domain interactions as a mechanism for the regulation of connexin channels. Circulation Research, 84(10), 1144-1155.

Hetero-domain interactions as a mechanism for the regulation of connexin channels. / Stergiopoulos, Kathleen; Alvarado, José Luis; Mastroianni, Marta; Ek Vitorin, Jose F; Taffet, Steven M.; Delmar, Mario.

In: Circulation Research, Vol. 84, No. 10, 28.05.1999, p. 1144-1155.

Research output: Contribution to journalArticle

Stergiopoulos, K, Alvarado, JL, Mastroianni, M, Ek Vitorin, JF, Taffet, SM & Delmar, M 1999, 'Hetero-domain interactions as a mechanism for the regulation of connexin channels', Circulation Research, vol. 84, no. 10, pp. 1144-1155.
Stergiopoulos K, Alvarado JL, Mastroianni M, Ek Vitorin JF, Taffet SM, Delmar M. Hetero-domain interactions as a mechanism for the regulation of connexin channels. Circulation Research. 1999 May 28;84(10):1144-1155.
Stergiopoulos, Kathleen ; Alvarado, José Luis ; Mastroianni, Marta ; Ek Vitorin, Jose F ; Taffet, Steven M. ; Delmar, Mario. / Hetero-domain interactions as a mechanism for the regulation of connexin channels. In: Circulation Research. 1999 ; Vol. 84, No. 10. pp. 1144-1155.
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