Class II and IV HDACs function as inhibitors of osteoclast differentiation.

Citation data:

PloS one, ISSN: 1932-6203, Vol: 12, Issue: 9, Page: e0185441

Publication Year:
2017
Usage 1278
Full Text Views 1261
Abstract Views 16
Link-outs 1
PMID:
28953929
DOI:
10.1371/journal.pone.0185441
Author(s):
Nicholas C. Blixt, Bora K. Faulkner, Kristina Astleford, Rosemary Lelich, Jacob Schering, Ekaterina Spencer, Rajaram Gopalakrishnan, Eric D. Jensen, Kim C. Mansky, Sakamuri V. Reddy
Publisher(s):
Public Library of Science (PLoS)
Tags:
Biochemistry, Genetics and Molecular Biology, Agricultural and Biological Sciences
article description
Histone deacetylases (HDACs) are negative regulators of transcription and have been shown to regulate specific changes in gene expression. In vertebrates, eighteen HDACs have thus far been identified and subdivided into four classes (I-IV). Key roles for several HDACs in bone development and biology have been elucidated through in vitro and in vivo models. By comparison, there is a paucity of data on the roles of individual HDACs in osteoclast formation and function. In this study, we investigated the gene expression patterns and the effects of suppressing individual class II (Hdac4, 5, 6, 9, and 10) and class IV (Hdac11) HDACs during osteoclast differentiation. We demonstrated that HDAC class II and IV members are differentially expressed during osteoclast differentiation. Additionally, individual shRNA-mediated suppression of Hdac4, 5, 9, 10 and 11 expression resulted in increased multinucleated osteoclast size and demineralization activity, with little to no change in the overall number of multinucleated osteoclasts formed compared with control shRNA-treated cells. We also detected increased expression of genes highly expressed in osteoclasts, including c-Fos, Nfatc1, Dc-stamp and Cathepsin K. These observations indicate that HDACs cooperatively regulate shared targets in a non-redundant manner.

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