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 Jeong; Park, Doo Ri; Bhattarai, Deepak; Lee, Kyeong; Kim, Jaesang; Bae, Yun Soo; Lee, 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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Collections - College of Pharmacy > Department of Pharmacy > 1. Journal Articles

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