Loss of Cbl-b increases osteoclast bone-resorbing activity and induces osteopenia

Arata Nakajima, Archana Sanjay, Riccardo Chiusaroli, Naga Suresh Adapala, Lynn Neff, Cecile Itzsteink, William C. Horne, Roland Baron

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Cbl proteins are multifunctional adaptor molecules that modulate cellular activity by targeting the ubiquitylating system, endocytic complexes, and other effectors to a wide variety of regulatory proteins, especially activated receptor and nonreceptor tyrosine kinases. Cbl and Cbl-b perform unique functions in various cells, in addition to redundant functions that are required for embryonic development. We previously showed that eliminating Cbl impaired osteoclast motility, which modestly delayed embryonic bone development. We now report that Cbl-b-/- mice are osteopenic, because of increased bone resorption with little compensating increase in bone formation. In vitro bone-resorbing activity and differentiation of osteoclast-like cells (OCLs) were increased, as were some RANKL-induced signaling events (activation of NF-κB and the mitogen-activated protein kinases extracellular signal-regulated kinase [ERK] and p38), suggesting that specific RANKL-activated mechanisms contribute to the increased rate of differentiation and bone-resorbing activity. Re-expressing Cbl-b in Cbl-b-/- OCLs normalized the increased bone-resorbing activity and overexpressing Cbl-b in wildtype OCLs inhibited bone resorption. Cbl was without effect in either wildtype or Cbl-b-/- OCLs. Functional tyrosine kinase binding (TKB) and RING finger domains were required for the rescue by Cbl-b. Thus, both Cbl and Cbl-b perform regulatory functions in osteoclasts that are unique to one or the other protein (i.e., functions that cannot be compensated by the other homolog). One of Cbl-b's unique functions in osteoclasts is to downregulate bone resorption.

Original languageEnglish (US)
Pages (from-to)1162-1172
Number of pages11
JournalJournal of Bone and Mineral Research
Volume24
Issue number7
DOIs
StatePublished - Jul 1 2009

Fingerprint

Metabolic Bone Diseases
Osteoclasts
Bone Resorption
Embryonic Development
RING Finger Domains
Proteins
Bone Development
Extracellular Signal-Regulated MAP Kinases
Receptor Protein-Tyrosine Kinases
bone resorption factor
Mitogen-Activated Protein Kinases
Osteogenesis
Protein-Tyrosine Kinases
Down-Regulation

Keywords

  • Bone resorption
  • Cbl-b
  • Differentiation
  • Osteoclast
  • Osteopenia

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Orthopedics and Sports Medicine

Cite this

Loss of Cbl-b increases osteoclast bone-resorbing activity and induces osteopenia. / Nakajima, Arata; Sanjay, Archana; Chiusaroli, Riccardo; Adapala, Naga Suresh; Neff, Lynn; Itzsteink, Cecile; Horne, William C.; Baron, Roland.

In: Journal of Bone and Mineral Research, Vol. 24, No. 7, 01.07.2009, p. 1162-1172.

Research output: Contribution to journalArticle

Nakajima, A, Sanjay, A, Chiusaroli, R, Adapala, NS, Neff, L, Itzsteink, C, Horne, WC & Baron, R 2009, 'Loss of Cbl-b increases osteoclast bone-resorbing activity and induces osteopenia', Journal of Bone and Mineral Research, vol. 24, no. 7, pp. 1162-1172. https://doi.org/10.1359/jbmr.090205
Nakajima, Arata ; Sanjay, Archana ; Chiusaroli, Riccardo ; Adapala, Naga Suresh ; Neff, Lynn ; Itzsteink, Cecile ; Horne, William C. ; Baron, Roland. / Loss of Cbl-b increases osteoclast bone-resorbing activity and induces osteopenia. In: Journal of Bone and Mineral Research. 2009 ; Vol. 24, No. 7. pp. 1162-1172.
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