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Cited 6 time in webofscience Cited 6 time in scopus
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2-(Trimethylammonium) Ethyl (R)-3-Methoxy-3-oxo-2-Stearamidopropyl Phosphate Suppresses Osteoclast Maturation and Bone Resorption by Targeting Macrophage-Colony Stimulating Factor Signalingopen access

Authors
Park, So JeongPark, Doo RiBhattarai, DeepakLee, KyeongKim, JaesangBae, Yun SooLee, Soo Young
Issue Date
31-Aug-2014
Publisher
KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
Keywords
antiresorptive drugs; bone destruction; osteoclast; osteoclast maturation; (R)-TEMOSPho
Citation
MOLECULES AND CELLS, v.37, no.8, pp 628 - 635
Pages
8
Indexed
SCI
SCIE
SCOPUS
KCI
Journal Title
MOLECULES AND CELLS
Volume
37
Number
8
Start Page
628
End Page
635
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/15254
DOI
10.14348/molcells.2014.0190
ISSN
1016-8478
0219-1032
Abstract
2-(Trimethylammonium) ethyl (R)/3-methoxy-3-oxo-2-steara-midopropyl phosphate [(R)-TEMOSPho], a derivative of an organic chemical identified from a natural product library, promotes highly efficient megakaryopoiesis. Here, we show that (R)-TEMOSPho blocks osteoclast maturation from progenitor cells of hematopoietic origin, as well as blocking the resorptive function of mature osteoclasts. The inhibitory effect of (R)-TEMOSPho on osteoclasts was due to a disruption of the actin cytoskeleton, resulting from impaired downstream signaling of c-Fms, a receptor for macrophage-colony stimulating factor linked to c-Cbl, phosphoinositol-3-kinase (PI3K), Vav3, and Rac1. In addition, (R)-TEMOSPho blocked inflammation-induced bone destruction by reducing the numbers of osteoclasts produced in mice. Thus, (R)-TEMOSPho may represent a promising new class of antiresorptive drugs for the treatment of bone loss associated with increased osteoclast maturation and activity.
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