4.3 Article

The effects of DNA methyltransferase inhibitors and histone deacetylase inhibitors on digit regeneration in mice

期刊

REGENERATIVE MEDICINE
卷 5, 期 2, 页码 201-220

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/RME.09.91

关键词

cell proliferation; epigenetics; Msx1; pharmacology; regeneration; regenerative medicine; retinoic acid; stem cells; transcription; wound healing

资金

  1. DOD/DARPA [UPIT W911NF 06-1-0067]
  2. University of Pittsburgh

向作者/读者索取更多资源

We injected two drugs that modify the epigenome, the DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine (5-aza-dC) and the histone deacetylase inhibitor trichostatin A (TSA), alone or in combination, into C57Bl/6 mice subjected to amputation through the mid-second phalanx of the third digit. Wound-site tissue was collected. Results: We observed increased staining of the stem cell markers Rex1 (Zfp42) and stem cell antigen-1 at digit amputation sites from drug-treated mice. Samples from 5-aza-dC plus TSA and TSA treated mice also showed increased proliferating cell nuclear antigen staining, a measure of cell proliferation. Drug treatments increased Msx1, but not Cyp26a1 or ALDH1a2 (RALDH2) mRNA. Conclusion: 5-aza-dC and TSA treatments stimulated cell proliferation at the amputation site, possibly via increased expression of genes involved in digit development and regeneration.

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