Regulation of Osteoclastogenesis and Bone Resorption by miRNAs
Osteoclasts are specialized bone-resorbing cells that contribute to physiological bone development and remodeling in bone metabolism throughout life. Abnormal production and activation of osteoclasts lead to excessive bone resorption in pathological conditions, such as in osteoporosis and in arthrit...
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Published in | Frontiers in cell and developmental biology Vol. 9; p. 651161 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
18.06.2021
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Subjects | |
Online Access | Get full text |
ISSN | 2296-634X 2296-634X |
DOI | 10.3389/fcell.2021.651161 |
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Summary: | Osteoclasts are specialized bone-resorbing cells that contribute to physiological bone development and remodeling in bone metabolism throughout life. Abnormal production and activation of osteoclasts lead to excessive bone resorption in pathological conditions, such as in osteoporosis and in arthritic diseases with bone destruction. Recent epigenetic studies have shed novel insight into the dogma of the regulation of gene expression. microRNAs belong to a category of epigenetic regulators, which post-transcriptionally regulate and silence target gene expression, and thereby control a variety of biological events. In this review, we discuss miRNA biogenesis, the mechanisms utilized by miRNAs, several miRNAs that play important roles in osteoclast differentiation, function, survival and osteoblast-to-osteoclast communication, and their translational potential and challenges in bone biology and skeletal diseases. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 This article was submitted to Cellular Biochemistry, a section of the journal Frontiers in Cell and Developmental Biology Reviewed by: Jiake Xu, University of Western Australia, Australia; Yankel Gabet, Tel Aviv University, Israel Edited by: Natalie A. Sims, University of Melbourne, Australia |
ISSN: | 2296-634X 2296-634X |
DOI: | 10.3389/fcell.2021.651161 |