» Articles » PMID: 23389618

WNT Signaling in Bone Homeostasis and Disease: from Human Mutations to Treatments

Overview
Journal Nat Med
Date 2013 Feb 8
PMID 23389618
Citations 922
Authors
Affiliations
Soon will be listed here.
Abstract

Low bone mass and strength lead to fragility fractures, for example, in elderly individuals affected by osteoporosis or children with osteogenesis imperfecta. A decade ago, rare human mutations affecting bone negatively (osteoporosis-pseudoglioma syndrome) or positively (high-bone mass phenotype, sclerosteosis and Van Buchem disease) have been identified and found to all reside in components of the canonical WNT signaling machinery. Mouse genetics confirmed the importance of canonical Wnt signaling in the regulation of bone homeostasis, with activation of the pathway leading to increased, and inhibition leading to decreased, bone mass and strength. The importance of WNT signaling for bone has also been highlighted since then in the general population in numerous genome-wide association studies. The pathway is now the target for therapeutic intervention to restore bone strength in millions of patients at risk for fracture. This paper reviews our current understanding of the mechanisms by which WNT signalng regulates bone homeostasis.

Citing Articles

Bone and muscle crosstalk in ageing and disease.

Kirk B, Lombardi G, Duque G Nat Rev Endocrinol. 2025; .

PMID: 40011751 DOI: 10.1038/s41574-025-01088-x.


Correlation between uric acid levels and bone mineral density in patients with type 2 diabetes mellitus: a systematic review and meta-analysis.

Zhao H, Qi C, Zhang Y, Ren L, Chen S Front Endocrinol (Lausanne). 2025; 16:1415550.

PMID: 39991737 PMC: 11842257. DOI: 10.3389/fendo.2025.1415550.


Synthetic Nanopillars for Stimulating Osteoblast Activity and Osteointegration in Bone-Related Disorders.

Liang W, Zhou C, Liu X, Xie Q, Xia L, Li Q Int J Nanomedicine. 2025; 20:2205-2223.

PMID: 39990287 PMC: 11847438. DOI: 10.2147/IJN.S501963.


Signaling Pathways Driving MSC Osteogenesis: Mechanisms, Regulation, and Translational Applications.

Wang L, Ruan M, Bu Q, Zhao C Int J Mol Sci. 2025; 26(3).

PMID: 39941080 PMC: 11818554. DOI: 10.3390/ijms26031311.


Methylase METTL3 regulates oxidative stress-induced osteoblast apoptosis through Wnt/β-catenin signaling pathway.

Yang P, Wang H, Meng L, Kou Y, Bu J, Li M J Mol Histol. 2025; 56(2):86.

PMID: 39928245 DOI: 10.1007/s10735-025-10358-x.


References
1.
McClung M, San Martin J, Miller P, Civitelli R, Bandeira F, Omizo M . Opposite bone remodeling effects of teriparatide and alendronate in increasing bone mass. Arch Intern Med. 2005; 165(15):1762-8. DOI: 10.1001/archinte.165.15.1762. View

2.
Gaur T, Wixted J, Hussain S, OConnell S, Morgan E, Ayers D . Secreted frizzled related protein 1 is a target to improve fracture healing. J Cell Physiol. 2009; 220(1):174-81. PMC: 2756719. DOI: 10.1002/jcp.21747. View

3.
Robling A, Kedlaya R, Ellis S, Childress P, Bidwell J, Bellido T . Anabolic and catabolic regimens of human parathyroid hormone 1-34 elicit bone- and envelope-specific attenuation of skeletal effects in Sost-deficient mice. Endocrinology. 2011; 152(8):2963-75. PMC: 3138236. DOI: 10.1210/en.2011-0049. View

4.
Baron R, Ferrari S, Russell R . Denosumab and bisphosphonates: different mechanisms of action and effects. Bone. 2010; 48(4):677-92. DOI: 10.1016/j.bone.2010.11.020. View

5.
Calvi L, Adams G, Weibrecht K, Weber J, Olson D, Knight M . Osteoblastic cells regulate the haematopoietic stem cell niche. Nature. 2003; 425(6960):841-6. DOI: 10.1038/nature02040. View