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. 2020 Sep 10;2020:8836258. doi: 10.1155/2020/8836258

Table 1.

DNA methylation in MSC aging and related diseases.

Regulatory factors Mechanism In vivo or in vitro Consequence Materials Ref.
Senescence and aging
DNMT1↓
DNMT3b↓
Decreases methylation in the promoter region of miRNA targeting Ezh2 to decrease Ezh2 expression, thus inhibiting repressive H3K27me3 formation at p16's promoter; directly decreases methylation in CDK inhibitor genes p16 and p21 In vitro Aging hUCSCs [28]
DNMT↓ Insufficient to methylate Tert promoter; thus upregulated TERT would repair the shortened telomeres with replication In vitro Antisenescence hBMSCs [30]
Skeletal diseases
DNMT1 changes Aberrant methylation of ABCB1 gene leads to a dysregulation of glucocorticoid In vitro ONFH hBMSCs [33]
TET1 and TET2↓ The depletion of TET causes impeded demethylation of P2rX7 promoter and incapable exosome release, which leads to intracellular accumulated miR-297 targeting Runx2 signaling pathway Both Osteoporosis hBMSCs, mouse BMSCs, mouse model [34]