4.7 Article

Primary Osteocyte Supernatants Metabolomic Profiling of Two Transgenic Mice With Connexin43 Dominant Negative Mutants

期刊

FRONTIERS IN ENDOCRINOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2021.649994

关键词

connexin43; osteocyte; hemichannel; metabolomics; metabolite

资金

  1. National Natural Science Foundation of China [81772409, 81472090]
  2. Space Medical Experiment Project of China Manned Space Program [HYZHXM01024]
  3. National Institutes of Health [AG045040]
  4. Welch Foundation [AQ-1507]

向作者/读者索取更多资源

Osteocytes can release small molecules through Cx43 channels, affecting metabolic pathways related to inflammation and oxidative stress. This study identified potential metabolites released by osteocytes through Cx43 channels, providing new insights into the regulatory mechanisms of osteocytes on themselves and other cells.
Osteocytes could release some small molecules (<= 1 kDa) through gap junctions and hemichannels to extracellular environment, such as prostaglandin E2 (PGE2), nitric oxide (NO) and adenosine triphosphate (ATP), which play key roles in transferring signals between bone cells and other tissue cells. Connexin (Cx) 43 is the most abundant connexin in osteocytes. To further discover molecules released by osteocytes through Cx43 channels and better understand the regulatory function of Cx43 channels in osteocytes, we performed non-targeted global metabolomics analysis using liquid chromatography-tandem mass spectrometry (LC-MS/MS) on conditioned medium collected from osteocytes isolated from two transgenic mouse models with Cx43 dominant negative mutants driven by a 10 kb-DMP1 promoter: R76W (gap junctions are blocked, whereas hemichannels are promoted) and Delta 130-136 (both gap junctions and hemichannels are blocked). The results revealed that several new categories of molecules, such as fatty acyls and carboxylic acids and derivatives, could be released through osteocytic Cx43 channels. In addition, alteration of Cx43 channel function affected the release of metabolites related to inflammatory reaction and oxidative stress. Pathway analysis further showed that citric acid cycle was the most differential metabolic pathway regulated by Cx43 channels. In sum, these results isolated new potential metabolites released by osteocytes through Cx43 channels, and offered a novel perspective to understand the regulatory mechanisms of osteocytes on themselves and other cells as well.

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