Elevated Intracellular Ca2+ Signals by Oxidative Stress Activate Connexin 43 Hemichannels in Osteocytes

Manuel A. Riquelme, Jean X. Jiang

Research output: Contribution to journalArticle

6 Scopus citations

Abstract

Elevated oxidative stress (OS) during aging leads to bone loss. OS increases intracellular Ca2+ ([Ca2+[ i), resulting in cellular damage and death. We show earlier that Cx43 hemichannels open in response to OS, which serves as a protective mechanism for osteocytes. However, the underlying mechanism is unknown. Here, we found that treatment with H 2 O 2 increased [Ca2+[ i in osteocytes with [Ca2+[ i being primarily derived from an extracellular Ca2+ source. Hemichannel opening induced by OS was inhibited by the depletion of [Ca2+[ i with BAPTA-AM, a Ca2+ chelator, suggesting that [Ca2+[ i influenced the activity of Cx43 hemichannels. Conversely, blockade of hemichannels had no effect on [Ca2+[ i. A biotinylation assay showed that cell surface-expressed Cx43 was increased by OS, which could be inhibited by BAPTA-AM, suggesting that [Ca2+[ i is necessary for Cx43 migration to the cell surface in response to OS. Together, these data suggest that increased hemichannel activity induced by OS was likely to be caused by elevated [Ca2+[ i through increased Cx43 on the cell surface.

Original languageEnglish (US)
Pages (from-to)355-361
Number of pages7
JournalBone Research
Volume1
DOIs
StatePublished - Dec 31 2013

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Keywords

  • Connexin hemichannels
  • calcium
  • osteocytes

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Histology

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