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Hdac3 Deficiency Increases Marrow Adiposity and Induces Lipid Storage and Glucocorticoid Metabolism in Osteochondroprogenitor Cells

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Bone loss and increased marrow adiposity are hallmarks of aging skeletons. Conditional deletion of histone deacetylase 3 (Hdac3) in murine osteochondroprogenitor cells causes osteopenia and increases marrow adiposity, even in young animals, but the origins of the increased adiposity are unclear. To explore this, bone marrow stromal cells (BMSCs) from Hdac3-depleted and control mice were cultured in osteogenic medium. Hdac3-deficient cultures accumulated lipid droplets in greater abundance than control cultures and expressed high levels of genes related to lipid storage (Fsp27/Cidec, Plin1) and glucocorticoid metabolism (Hsd11b1) despite normal levels of PPARγ2. Approximately 5% of the lipid containing cells in the wild-type cultures expressed the master osteoblast transcription factor Runx2, but this population was threefold greater in the Hdac3-depleted cultures. Adenoviral expression of Hdac3 restored normal gene expression, indicating that Hdac3 controls glucocorticoid activation and lipid storage within osteoblast lineage cells. HDAC3 expression was reduced in bone cells from postmenopausal as compared to young women, and in osteoblasts from aged as compared to younger mice. Moreover, phosphorylation of S424 in Hdac3, a posttranslational mark necessary for deacetylase activity, was suppressed in osseous cells from old mice. Thus, concurrent declines in transcription and phosphorylation combine to suppress Hdac3 activity in aging bone, and reduced Hdac3 activity in osteochondroprogenitor cells contributes to increased marrow adiposity associated with aging.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 116-128 (13 pages)

Journal (Volume, Issue Number)

Journal of Bone and Mineral Research (Volume 31, Issue 1)

Publication milestones

  • Published - 01/01/2016

Publication status

Published - 01/01/2016

ISSN

0884-0431

Publication IDs

  • Scopus: 84957432124
  • PubMed: 26211746

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
2.89
SciVal
Author count
9
SciVal
citations
40
SciVal
Paper percentile
94
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.11
Fractional count
8
Fractional count
0.89
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
40
Citation count
64

Funding Details

This work was supported by grants from the NIH (T32 AR056950, F32 AR60140, AG004875), Minnesota Obesity Center (Subaward H412621701, P30DK050456-18), Mayo Foundation of Education and Research, Mayo Graduate School, and Mayo Clinic Center for Regenerative Medicine. Hsd11b1-luciferase constructs were a kind gift from Dr. Karen Chapman. We thank Dr. David Razidlo and Bridget Stensgard for mouse colony maintenance; Xiaodong Li, Samuel Carlson, and Calley Jones for technical assistance; and the Mayo Clinic Biomaterials and Quantitative Histomorphometry Core Laboratory for assistance with histological specimen preparation. Authors’ roles: Study design: MEML and JJW. Study conduct: MEML, LRC, RJS, JNF, and JLP. Data collection: MEML, LRC, RJS, JNF, and JLP. Data analysis: MEML, LRC, RJS, JNF, JLP, and JJW. Data interpretation: MEML, LRC, RJS, SK, and JJW. Drafting manuscript: MEML and JJW. Revising manuscript content: MEML, LRC, RJS, JNF, JLP, SK, MJO, and JJW. Approving final version of manuscript: MEML, LRC, RJS, JNF, JLP, MJM, SK, MJO, and JJW. MEML and JJW take responsibility for the integrity of the data analysis. This work was supported by grants from the NIH (T32 AR056950, F32 AR60140, AG004875), Minnesota Obesity Center (Subaward H412621701, P30DK050456-18), Mayo Foundation of Education and Research, Mayo Graduate School, and Mayo Clinic Center for Regenerative Medicine. Hsd11b1-luciferase constructs were a kind gift from Dr. Karen Chapman. We thank Dr. David Razidlo and Bridget Stensgard for mouse colony maintenance; Xiaodong Li, Samuel Carlson, and Calley Jones for technical assistance; and the Mayo Clinic Biomaterials and Quantitative Histomorphometry Core Laboratory for assistance with histological specimen preparation. Authors? roles: Study design: MEML and JJW. Study conduct: MEML, LRC, RJS, JNF, and JLP. Data collection: MEML, LRC, RJS, JNF, and JLP. Data analysis: MEML, LRC, RJS, JNF, JLP, and JJW. Data interpretation: MEML, LRC, RJS, SK, and JJW. Drafting manuscript: MEML and JJW. Revising manuscript content: MEML, LRC, RJS, JNF, JLP, SK, MJO, and JJW. Approving final version of manuscript: MEML, LRC, RJS, JNF, JLP, MJM, SK, MJO, and JJW. MEML and JJW take responsibility for the integrity of the data analysis.
FundersFunding numbers
Minnesota Obesity Center, University of Minnesota
H412621701, P30DK050456-18
NIH
-
NIA
P01AG004875
NIDDK
P30DK050456
NIAMS
F32AR060140, T32AR056950
Department of Immunology, Mayo Clinic College of Medicine, Mayo Clinic
-
JNF
-