Ilimaquinone inhibits gap junctional communication in a connexin isotype-specific manner

V. Cruciani, S.-O. Mikalsen

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

Ilimaquinone (IQ) and brefeldin A (BFA) disrupt the Golgi complex structure and block protein transport to the plasma membrane, and inhibit gap junctional communication. HeLa cells expressing rat connexin26, 32, or 43, or mouse connexin31, 36, 45, or 57, were used to study the response patterns of gap junctional communication (dye transfer) to ilimaquinone, brefeldin, and the potent protein kinase C (PKC) activator 12-O-tetradecanoylphorbol-13-acetate (TPA). 12-O-Tetradecanoylphorbol-13-acetate (followed for 2 h) caused dose- and time-dependent decreases in communication for five of seven connexins, the unresponsive being connexin45 and 57. Brefeldin (followed for 6 h) caused dose- and time-dependent decreases in communication for six of seven connexins, the exception being connexin26. These results are consistent with Golgi-mediated transport to the cell membrane for all connexins except connexin26. In contrast, ilimaquinone (followed for 6 h) caused a rapid (15–30 min) and nearly complete inhibition of dye transfer through connexin43 channels. For the other connexins, there was a slow and weak response for connexin26, 31, and 32, reaching 65–70% of control communication level, while connexin36, 45, and 57 were unresponsive. Thus, among the tested connexins, ilimaquinone has a strong specificity for connexin43, and the mechanism appears independent of the Golgi complex and of protein kinase C.
Original languageEnglish
Pages (from-to)136-148
Number of pages13
JournalExperimental Cell Research
Volume304
Issue number1
DOIs
Publication statusPublished - 2005

Keywords

  • Connexin
  • Connexin 43
  • Brefeldin A
  • Gap junctional intercellular communication
  • Golgi
  • Ilimaquinone
  • protein kinase c

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