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 PMID:29858571  

Tet1 and Tet2 maintain mesenchymal stem cell homeostasis via demethylation of the P2rX7 promoter.

Ruili Yang | Tingting Yu | Xiaoxing Kou | Xiang Gao | Chider Chen | Dawei Liu | Yanheng Zhou | Songtao Shi
Nature communications | 2018

Ten-eleven translocation (Tet) family-mediated DNA oxidation represents an epigenetic modification capable of converting 5-methylcytosine (5-mC) to 5-hydroxymethylcytosine (5-hmC), which regulates various biological processes. However, it is unknown whether Tet family affects mesenchymal stem cells (MSCs) or the skeletal system. Here we show that depletion of Tet1 and Tet2 results in impaired self-renewal and differentiation of bone marrow MSCs (BMMSCs) and a significant osteopenia phenotype. Tet1 and Tet2 deficiency reduces demethylation of the P2rX7 promoter and downregulates exosome release, leading to intracellular accumulation of miR-297a-5p, miR-297b-5p, and miR-297c-5p. These miRNAs inhibit Runx2 signaling to impair BMMSC function. We show that overexpression of P2rX7 rescues the impaired BMMSCs and osteoporotic phenotype in Tet1 and Tet2 double knockout mice. These results indicate that Tet1 and Tet2 play a critical role in maintaining BMMSC and bone homeostasis through demethylation of P2rX7 to control exosome and miRNA release. This Tet/P2rX7/Runx2 cascade may serve as a target for the development of novel therapies for osteopenia disorders.

Pubmed ID: 29858571

Associated grants

  • Agency: NIAMS NIH HHS, United States
    Id: P30 AR069619
  • Agency: NIDCR NIH HHS, United States
    Id: R01 DE017449
  • Agency: NIDCR NIH HHS, United States
    Id: R03 DE028026
  • Agency: NIDCR NIH HHS, United States
    Id: K99 DE025915
  • Agency: NIAMS NIH HHS, United States
    Id: T32 AR007442
  • Agency: NIDCR NIH HHS, United States
    Id: R00 DE025915

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