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Table 2 Histone acetylation and related modifiers regulate the fate of BM-MSC

From: Dysregulation of histone modifications in bone marrow mesenchymal stem cells during skeletal ageing: roles and therapeutic prospects

Modifiers

Histone modification

Targets

Effects on fate of BM-MSC (in vitro)

Effects on bone (in vivo)

References

Acetylases

     

GCN5 (KAT2A)

H3K9ac

Vegf, Wnt

Promotes angiogenesis and osteogenesis

Inhibits bone loss

[85, 88]

PCAF (KAT2B)

H3K9ac

BMP2, BMP4, BMPR1B, RUNX2

Promotes osteogenesis

Not evaluated

[86]

p300 (KAT3B)

H3K9ac

H3K27ac

α-KG

Inhibits osteogenesis

Not evaluated

[98, 99]

p300/CBP

H3K27ac

Pparγ, p53, p21Cip1

Promotes adipogenesis and senescence

Not evaluated

[100]

Deacetylases

     

HDAC1

H3/H4ac

Pparγ2, C/ebpα

Inhibits adipogenesis

Not evaluated

[64, 84]

HDAC1

H3ac

Jag1

Inhibits osteogenesis

Promotes bone loss

[109]

HDAC6

H3K9/K14ac

H4K12ac

Runx2

Inhibits osteogenesis

Promotes age-related bone loss

[91]

HDAC9

H3K9ac

Atg7

Becn1

LC3a/b

Promotes adipogenesis while inhibiting autophagy and osteogenesis

Promotes age-related bone loss

[92]

HDAC11

H3K9ac

Hsd11b2

Inhibits osteogenesis

Not evaluated

[93]

SIRT1

H3K14ac

Runx2

Sp7

Bglap

Inhibits osteogenesis

Not evaluated

[94]

SIRT7

H3K18ac

OSX

Inhibits osteogenesis

Not evaluated

[101]

Other regulators

     

NAMPT

H3K9ac

Runx2

Promotes osteogenesis

Not evaluated

[87]

  1. Not evaluated: the effects of histone modification enzymes or related modifiers on bone were not verified in vivo