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Syk, c-Src, the alphavbeta3 integrin, and ITAM immunoreceptors, in concert, regulate osteoclastic bone resorption.

Abstract
In this study, we establish that the tyrosine kinase Syk is essential for osteoclast function in vitro and in vivo. Syk(-/-) osteoclasts fail to organize their cytoskeleton, and, as such, their bone-resorptive capacity is arrested. This defect results in increased skeletal mass in Syk(-/-) embryos and dampened basal and stimulated bone resorption in chimeric mice whose osteoclasts lack the kinase. The skeletal impact of Syk deficiency reflects diminished activity of the mature osteoclast and not impaired differentiation. Syk regulates bone resorption by its inclusion with the alpha v beta3 integrin and c-Src in a signaling complex, which is generated only when alpha v beta3 is activated. Upon integrin occupancy, c-Src phosphorylates Syk. Alpha v beta3-induced phosphorylation of Syk and the latter's capacity to associate with c-Src is mediated by the immunoreceptor tyrosine-based activation motif (ITAM) proteins Dap12 and FcRgamma. Thus, in conjunction with ITAM-bearing proteins, Syk, c-Src, and alpha v beta3 represent an essential signaling complex in the bone-resorbing osteoclast, and, therefore, each is a candidate therapeutic target.
AuthorsWei Zou, Hideki Kitaura, Jennifer Reeve, Fanxin Long, Victor L J Tybulewicz, Sanford J Shattil, Mark H Ginsberg, F Patrick Ross, Steven L Teitelbaum
JournalThe Journal of cell biology (J Cell Biol) Vol. 176 Issue 6 Pg. 877-88 (Mar 12 2007) ISSN: 0021-9525 [Print] United States
PMID17353363 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Integrin alphaVbeta3
  • Intracellular Signaling Peptides and Proteins
  • Receptors, Immunologic
  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins pp60(c-src)
  • SYK protein, human
  • Syk Kinase
  • Syk protein, mouse
Topics
  • Amino Acid Motifs
  • Animals
  • Bone Resorption (enzymology, pathology)
  • Cell Differentiation
  • Chimera (metabolism)
  • Humans
  • Integrin alphaVbeta3 (metabolism, physiology)
  • Intracellular Signaling Peptides and Proteins (genetics, metabolism, physiology)
  • Mice
  • Molecular Sequence Data
  • Osteoclasts (enzymology, pathology, physiology)
  • Phosphorylation
  • Protein-Tyrosine Kinases (genetics, metabolism, physiology)
  • Proto-Oncogene Proteins pp60(c-src) (metabolism, physiology)
  • Receptors, Immunologic (chemistry, metabolism, physiology)
  • Sequence Alignment
  • Syk Kinase

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