Talin1 and Rap1 are critical for osteoclast function

Wei Zou, Takashi Izawa, Tingting Zhu, Jean Chappel, Karel Otero, Susan J. Monkley, David R. Critchley, Brian G. Petrich, Alexei Morozov, Mark H. Ginsberg, Steven L. Teitelbaum

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

To determine talin1's role in osteoclasts, we mated TLN1fl/fl mice with those expressing cathepsin K-Cre (CtsK-TLN1) to delete the gene in mature osteoclasts or with lysozyme M-Cre (LysM-TLN1) mice to delete TLN1 in all osteoclast lineage cells. Absence of TLN1 impairs macrophage colony-stimulating factor (M-CSF)-stimulated inside-out integrin activation and cytoskeleton organization in mature osteoclasts. Talin1-deficient precursors normally express osteoclast differentiation markers when exposed to M-CSF and receptor activator of nuclear factor κB (RANK) ligand but attach to substrate and migrate poorly, arresting their development into mature resorptive cells. In keeping with inhibited resorption, CtsK-TLN1 mice exhibit an~5-fold increase in bone mass. Osteoclast-specific deletion of Rap1 (CtsK-Rap1), which promotes talin/β integrin recognition, yields similar osteopetrotic mice. The fact that the osteopetrosis of CtsK-TLN1 and CtsK-Rap1 mice is substantially more severe than that of those lacking αvβ3 is likely due to added failed activation of β1 integrins. In keeping with osteoclast dysfunction, mice in whom talin is deleted late in the course of osteoclastogenesis are substantially protected from ovariectomy-induced osteoporosis and the periarticular osteolysis attending inflammatory arthritis. Thus, talin1 and Rap1 are critical for resorptive function, and their selective inhibition in mature osteoclasts retards pathological bone loss.

Original languageEnglish
Pages (from-to)830-844
Number of pages15
JournalMolecular and Cellular Biology
Volume33
Issue number4
DOIs
Publication statusPublished - Feb 1 2013
Externally publishedYes

Fingerprint

Osteoclasts
Integrins
Talin
Macrophage Colony-Stimulating Factor Receptors
Cathepsin K
RANK Ligand
Osteopetrosis
Bone and Bones
Osteolysis
Macrophage Colony-Stimulating Factor
Differentiation Antigens
Ovariectomy
Muramidase
Cytoskeleton
Osteogenesis
Osteoporosis
Arthritis
Genes

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

Zou, W., Izawa, T., Zhu, T., Chappel, J., Otero, K., Monkley, S. J., ... Teitelbaum, S. L. (2013). Talin1 and Rap1 are critical for osteoclast function. Molecular and Cellular Biology, 33(4), 830-844. https://doi.org/10.1128/MCB.00790-12

Talin1 and Rap1 are critical for osteoclast function. / Zou, Wei; Izawa, Takashi; Zhu, Tingting; Chappel, Jean; Otero, Karel; Monkley, Susan J.; Critchley, David R.; Petrich, Brian G.; Morozov, Alexei; Ginsberg, Mark H.; Teitelbaum, Steven L.

In: Molecular and Cellular Biology, Vol. 33, No. 4, 01.02.2013, p. 830-844.

Research output: Contribution to journalArticle

Zou, W, Izawa, T, Zhu, T, Chappel, J, Otero, K, Monkley, SJ, Critchley, DR, Petrich, BG, Morozov, A, Ginsberg, MH & Teitelbaum, SL 2013, 'Talin1 and Rap1 are critical for osteoclast function', Molecular and Cellular Biology, vol. 33, no. 4, pp. 830-844. https://doi.org/10.1128/MCB.00790-12
Zou, Wei ; Izawa, Takashi ; Zhu, Tingting ; Chappel, Jean ; Otero, Karel ; Monkley, Susan J. ; Critchley, David R. ; Petrich, Brian G. ; Morozov, Alexei ; Ginsberg, Mark H. ; Teitelbaum, Steven L. / Talin1 and Rap1 are critical for osteoclast function. In: Molecular and Cellular Biology. 2013 ; Vol. 33, No. 4. pp. 830-844.
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