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Histone acetylation together with DNA demethylation empowers higher plasticity in adipocytes to differentiate into osteoblasts.
- Source :
-
Gene [Gene] 2020 Apr 05; Vol. 733, pp. 144274. Date of Electronic Publication: 2019 Dec 03. - Publication Year :
- 2020
-
Abstract
- Bone regeneration has been a challenge for both researchers and clinicians. In the field of tissue engineering, much effort has been made to identify cell sources including stem cells. The present study aimed to induce trans-differentiation from adipocytes to osteoblasts using epigenetic modifiers; 5-aza-dC and/or trichostatin-A (TSA). 3 T3-L1 preadipocytes were treated with TSA (100 nM) and then with Wnt3a (50 ng/ml). Microscopic observation showed trans-differentiated cell morphology. Methylation-specific PCR and immunoblotting were performed to analyze the DNA methylation and histone acetylation patterns. The gene expression was determined by real-time PCR. Based on these in vitro experiments, in vivo mouse experiments supplemented the possibility of trans-differentiation by epigenetic modification. TSA induced the acetylation of lysine9 on histone H3, and a sequential Wnt3a treatment stimulated the expression of bone marker genes in adipocytes, suppressing adipogenesis and stimulating osteogenesis. Furthermore, TSA induced DNA hypomethylation, and a combined treatment with TSA and 5-aza-dC showed a synergistic effect in epigenetic modifications. The number of adipocytes and DNA methylation patterns of old (15 months) and young (6 weeks) mice were significantly different, and TSA and sequential Wnt3a treatments increased bone formation in the old mice. Collectively, our results confirmed cell trans-differentiation via epigenetic modifications and osteogenic signaling from adipocytes to osteoblasts for the bone regeneration in vitro and in vivo, and indicated that histone acetylation could induce DNA hypomethylation, enhancing the chance of trans-differentiation.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2019 Elsevier B.V. All rights reserved.)
- Subjects :
- 3T3-L1 Cells
Acetylation
Adipocytes drug effects
Animals
Cell Differentiation genetics
Cell Differentiation physiology
CpG Islands
DNA Demethylation drug effects
DNA Methylation drug effects
DNA Methylation genetics
Decitabine metabolism
Decitabine pharmacology
Epigenesis, Genetic drug effects
Epigenesis, Genetic genetics
Epigenomics methods
Histone Deacetylase Inhibitors pharmacology
Histones genetics
Histones metabolism
Hydroxamic Acids metabolism
Hydroxamic Acids pharmacology
Mice
Osteoblasts drug effects
Promoter Regions, Genetic drug effects
Promoter Regions, Genetic genetics
Protein Processing, Post-Translational drug effects
Protein Processing, Post-Translational genetics
Adipocytes metabolism
Cell Differentiation drug effects
Osteoblasts metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0038
- Volume :
- 733
- Database :
- MEDLINE
- Journal :
- Gene
- Publication Type :
- Academic Journal
- Accession number :
- 31809844
- Full Text :
- https://doi.org/10.1016/j.gene.2019.144274