Osteoblast mineralization requires β1 integrin/ICAP-1–dependent fibronectin deposition

Autor: Genevieve Chevalier, Inaam A. Nakchbandi, Molly Brunner, Angélique Millon-Frémillon, Daniel Bouvard, Marc R. Block, Deane F. Mosher, Corinne Albiges-Rizo
Přispěvatelé: Institut d'oncologie/développement Albert Bonniot de Grenoble (INSERM U823), Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM), Dynamique des systèmes d'adhérence et différenciation (DySAD), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Department of Molecular Medicine [Martinsreid], Max Planck Institute of Biochemistry (MPIB), Max-Planck-Gesellschaft-Max-Planck-Gesellschaft, School of Medicine and Public Health, University of Wisconsin-Madison, Pro-A INSERM, Ligue Nationale Contre le cancer (DB), NIH HL21644 (DM), Block, Marc, Max-Planck-Institut für Biochemie = Max Planck Institute of Biochemistry (MPIB)
Jazyk: angličtina
Rok vydání: 2011
Předmět:
ICAP-1
integrin
Cellular differentiation
Integrin
Immunology
Muscle Proteins
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Mineralization (biology)
Article
osteogenesis
Extracellular matrix
03 medical and health sciences
Mice
0302 clinical medicine
Calcification
Physiologic

medicine
Immunology and Allergy
Animals
mineralization
Cytoskeleton
[SDV.BC] Life Sciences [q-bio]/Cellular Biology
Research Articles
030304 developmental biology
Cell Proliferation
0303 health sciences
kindlin
Osteoblasts
biology
Integrin beta1
β1 integrin
Intracellular Signaling Peptides and Proteins
Correction
Osteoblast
Cell Differentiation
Cell Biology
Fibronectins
Cell biology
Extracellular Matrix
Fibronectin
Cytoskeletal Proteins
medicine.anatomical_structure
biology.protein
fibrilogenesis
Type I collagen
030217 neurology & neurosurgery
Protein Binding
Zdroj: The Journal of Cell Biology
Journal of Cell Biology
Journal of Cell Biology, Rockefeller University Press, 2011, 194 (2), pp.307-22. ⟨10.1083/jcb.201007108⟩
Journal of Cell Biology, 2011, 194 (2), pp.307-22. ⟨10.1083/jcb.201007108⟩
ISSN: 1540-8140
0021-9525
Popis: ICAP-1 prevents recruitment of kindlin-2 to β1 integrin to control dynamics of fibrillar adhesion sites, fibronectin deposition, and osteoblast mineralization during bone formation.
The morphogenetic and differentiation events required for bone formation are orchestrated by diffusible and insoluble factors that are localized within the extracellular matrix. In mice, the deletion of ICAP-1, a modulator of β1 integrin activation, leads to severe defects in osteoblast proliferation, differentiation, and mineralization and to a delay in bone formation. Deposition of fibronectin and maturation of fibrillar adhesions, adhesive structures that accompany fibronectin deposition, are impaired upon ICAP-1 loss, as are type I collagen deposition and mineralization. Expression of β1 integrin with a mutated binding site for ICAP-1 recapitulates the ICAP-1–null phenotype. Follow-up experiments demonstrated that ICAP-1 negatively regulates kindlin-2 recruitment onto the β1 integrin cytoplasmic domain, whereas an excess of kindlin-2 binding has a deleterious effect on fibrillar adhesion formation. These results suggest that ICAP-1 works in concert with kindlin-2 to control the dynamics of β1 integrin–containing fibrillar adhesions and, thereby, regulates fibronectin deposition and osteoblast mineralization.
Databáze: OpenAIRE