» Articles » PMID: 33297501

Deciphering the Relevance of Bone ECM Signaling

Overview
Journal Cells
Publisher MDPI
Date 2020 Dec 10
PMID 33297501
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Bone mineral density, a bone matrix parameter frequently used to predict fracture risk, is not the only one to affect bone fragility. Other factors, including the extracellular matrix (ECM) composition and microarchitecture, are of paramount relevance in this process. The bone ECM is a noncellular three-dimensional structure secreted by cells into the extracellular space, which comprises inorganic and organic compounds. The main inorganic components of the ECM are calcium-deficient apatite and trace elements, while the organic ECM consists of collagen type I and noncollagenous proteins. Bone ECM dynamically interacts with osteoblasts and osteoclasts to regulate the formation of new bone during regeneration. Thus, the composition and structure of inorganic and organic bone matrix may directly affect bone quality. Moreover, proteins that compose ECM, beyond their structural role have other crucial biological functions, thanks to their ability to bind multiple interacting partners like other ECM proteins, growth factors, signal receptors and adhesion molecules. Thus, ECM proteins provide a complex network of biochemical and physiological signals. Herein, we summarize different ECM factors that are essential to bone strength besides, discussing how these parameters are altered in pathological conditions related with bone fragility.

Citing Articles

Electro-spun piezoelectric PLLA smart composites as a scaffold on bone fracture: A review.

Mirghaffari M, Mahmoodiyan A, Mahboubizadeh S, Shahbazi A, Soleimani Y, Mirghaffari S Regen Ther. 2025; 28:591-605.

PMID: 40061293 PMC: 11889349. DOI: 10.1016/j.reth.2025.01.026.


Curcumin's protective role against fluoride-induced bone damage: Implications for pullet pathology and skeletal biomechanics.

Zuo Q, Meng H, Ommati M, Yang G, Zhao W, Zhao J Poult Sci. 2025; 104(3):104891.

PMID: 39970518 PMC: 11879666. DOI: 10.1016/j.psj.2025.104891.


Impact of High Glucose on Bone Collagenous Matrix Composition, Structure, and Organization: An Integrative Analysis Using an Ex Vivo Model.

Araujo R, Pascoa R, Bernardino R, Gomes P Cells. 2025; 14(2).

PMID: 39851558 PMC: 11764406. DOI: 10.3390/cells14020130.


Enhanced bacteriostasis and osseointegrative properties of SiRNA-modified polyetheretherketone surface for implant applications.

Liu Z, Yang L, Ni Y, Chen K, Yan Q, Zhao Z PLoS One. 2024; 19(12):e0314091.

PMID: 39636795 PMC: 11620434. DOI: 10.1371/journal.pone.0314091.


Self-Assembled Nanoparticles with Well-Defined Oligosaccharide Promote Osteogenesis by Regulating Golgi Stress Response.

Niu P, Zhao L, Yang J, Ding Y, Xu X, Li S Adv Healthc Mater. 2024; 14(3):e2402976.

PMID: 39618007 PMC: 11773123. DOI: 10.1002/adhm.202402976.


References
1.
Korvala J, Juppner H, Makitie O, Sochett E, Schnabel D, Mora S . Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. BMC Med Genet. 2012; 13:26. PMC: 3374890. DOI: 10.1186/1471-2350-13-26. View

2.
Visweswaran M, Pohl S, Arfuso F, Newsholme P, Dilley R, Pervaiz S . Multi-lineage differentiation of mesenchymal stem cells - To Wnt, or not Wnt. Int J Biochem Cell Biol. 2015; 68:139-47. DOI: 10.1016/j.biocel.2015.09.008. View

3.
Arkadash V, Yosef G, Shirian J, Cohen I, Horev Y, Grossman M . Development of High Affinity and High Specificity Inhibitors of Matrix Metalloproteinase 14 through Computational Design and Directed Evolution. J Biol Chem. 2017; 292(8):3481-3495. PMC: 5336179. DOI: 10.1074/jbc.M116.756718. View

4.
Li X, Liu D, Li J, Yang S, Xu J, Yokota H . Wnt3a involved in the mechanical loading on improvement of bone remodeling and angiogenesis in a postmenopausal osteoporosis mouse model. FASEB J. 2019; 33(8):8913-8924. PMC: 9272758. DOI: 10.1096/fj.201802711R. View

5.
Clarke B . Normal bone anatomy and physiology. Clin J Am Soc Nephrol. 2008; 3 Suppl 3:S131-9. PMC: 3152283. DOI: 10.2215/CJN.04151206. View