Erucin inhibits osteoclast formation via suppressing cell–cell fusion molecule DC-STAMP without influencing mineralization by osteoblasts

Bibliographic Details
Title: Erucin inhibits osteoclast formation via suppressing cell–cell fusion molecule DC-STAMP without influencing mineralization by osteoblasts
Authors: Tomohiro Takagi, Hirofumi Inoue, Shungo Fujii, Nobuyuki Takahashi, Mariko Uehara
Source: BMC Research Notes, Vol 15, Iss 1, Pp 1-6 (2022)
Publisher Information: BMC, 2022.
Publication Year: 2022
Collection: LCC:Medicine
LCC:Biology (General)
LCC:Science (General)
Subject Terms: Erucin, Isothiocyanate, Osteoclast differentiation, Osteoclast cell fusion, DC-STAMP, Medicine, Biology (General), QH301-705.5, Science (General), Q1-390
More Details: Abstract Objective Erucin (ERN), an isothiocyanate, is derived from the vegetable arugula. Although ERN has antitumor and antioxidant activity, the effect of ERN on osteoclast and osteoblast differentiation is not well documented. In this study, we evaluated the effects of ERN on osteoclast and osteoblast differentiation in vitro. Results ERN significantly reduced the formation of 1α,25(OH)2D3-induced tartrate-resistant acid phosphatase (TRAP)-positive cells at non-cytotoxic concentrations. Furthermore, ERN downregulated the mRNA expression of osteoclast-associated genes, such as nuclear factor of activated T cells cytoplasmic-1, TRAP, and cathepsin K. In addition, ERN suppressed mRNA expression of dendritic cell specific transmembrane protein (DC-STAMP), which encodes cell–cell fusion. However, ERN did not affect mineralization by osteoblasts. Thus, our data suggest that ERN may attenuate osteoclastic bone resorption by inhibiting multinucleation of mononuclear pre-osteoclasts and by suppressing mRNA expression of DC-STAMP in bone marrow cells without influencing mineralization by osteoblasts.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1756-0500
Relation: https://doaj.org/toc/1756-0500
DOI: 10.1186/s13104-022-05988-3
Access URL: https://doaj.org/article/e4487edba674456e89c6ef374b98e641
Accession Number: edsdoj.4487edba674456e89c6ef374b98e641
Database: Directory of Open Access Journals
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More Details
ISSN:17560500
DOI:10.1186/s13104-022-05988-3
Published in:BMC Research Notes
Language:English