Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/119902
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Type: Journal article
Title: Histone deacetylases 1 and 2 inhibition suppresses cytokine production and osteoclast bone resorption in vitro
Author: Algate, K.
Haynes, D.
Fitzsimmons, T.
Romeo, O.
Wagner, F.
Holson, E.
Reid, R.
Fairlie, D.
Bartold, P.
Cantley, M.
Citation: Journal of cellular biochemistry, 2019; OnlinePubl(1):1-15
Publisher: Wiley
Issue Date: 2019
ISSN: 0730-2312
1097-4644
Statement of
Responsibility: 
Kent Algate, David Haynes, Tracy Fitzsimmons, Ornella Romeo, Florence Wagner, Edward Holson, Robert Reid, David Fairlie, Peter Bartold, Melissa Cantley
Abstract: The regulation of epigenetic factors is an emerging therapeutic target of immune function in a variety of osteolytic pathologies. Histone deacetylases (HDAC) modify core histone proteins and transcriptional processes, in addition to nonhistone protein activity. The activated immune response in rheumatoid arthritis, periodontitis, and prosthetic implant particle release stimulates the catabolic activity of osteoclasts. In this study, we investigated the effects of novel therapeutic agents targeting HDAC isozymes (HDAC 1, 2, and 5), previously shown to be upregulated in inflammatory bone disorders, in cytokine-stimulated human monocytes and osteoclasts in vitro. Inhibiting HDAC 1 and 2 significantly reduced gene expression of IL-1β, TNF, MCP-1, and MIP-1α in TNF-stimulated monocytes, while suppressing secretions of IL-1β, IL-10, INF-γ, and MCP-1 (P < .05). Osteoclast formation and bone resorption were also significantly diminished with HDAC 1 and 2 inhibition, through reduced NFATc1 expression and osteoclast specific target genes, TRAF6, CTR, TRAP, and Cathepsin K (P < .05). Similar trends were observed when inhibiting HDAC 1 and to a lesser extent, HDAC 2, in isolation. However, their combined inhibition had the greatest anti-inflammatory and antiosteoclastic effects. Targeting HDAC 5 had minimal effects on these processes investigated in this study, whereas a broad acting HDACi, 1179.4b, had widespread suppressive outcomes. This study demonstrates that targeting HDACs is a potent and effective way of regulating the inflammatory and catabolic processes in human monocytes and osteoclasts. It also demonstrates the importance of targeting individual HDACs with an overall aim to improve efficiency and reduce any potential off target effects.
Keywords: bone loss; epigenetics; histone deacetylases (HDAC); inflammation; osteoclasts; tumor necrosis factor (TNF)
Rights: © 2019 Wiley Periodicals, Inc.
RMID: 0030119435
DOI: 10.1002/jcb.29137
Grant ID: http://purl.org/au-research/grants/nhmrc/1070880
http://purl.org/au-research/grants/nhmrc/1057835
Appears in Collections:Biochemistry publications

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