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Sequential and Opposing Activities of Wnt and BMP Coordinate Zebrafish Bone Regeneration

Overview
Journal Cell Rep
Publisher Cell Press
Date 2014 Feb 4
PMID 24485659
Citations 57
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Abstract

Zebrafish fully regenerate lost bone, including after fin amputation, through a process mediated by dedifferentiated, lineage-restricted osteoblasts. Mechanisms controlling the osteoblast regenerative program from its initiation through reossification are poorly understood. We show that fin amputation induces a Wnt/β-catenin-dependent epithelial to mesenchymal transformation (EMT) of osteoblasts in order to generate proliferative Runx2(+) preosteoblasts. Localized Wnt/β-catenin signaling maintains this progenitor population toward the distal tip of the regenerative blastema. As they become proximally displaced, preosteoblasts upregulate sp7 and subsequently mature into re-epithelialized Runx2(-)/sp7(+) osteoblasts that extend preexisting bone. Autocrine bone morphogenetic protein (BMP) signaling promotes osteoblast differentiation by activating sp7 expression and counters Wnt by inducing Dickkopf-related Wnt antagonists. As such, opposing activities of Wnt and BMP coordinate the simultaneous demand for growth and differentiation during bone regeneration. This hierarchical signaling network model provides a conceptual framework for understanding innate bone repair and regeneration mechanisms and rationally designing regenerative therapeutics.

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References
1.
Dorsky R, Sheldahl L, Moon R . A transgenic Lef1/beta-catenin-dependent reporter is expressed in spatially restricted domains throughout zebrafish development. Dev Biol. 2002; 241(2):229-37. DOI: 10.1006/dbio.2001.0515. View

2.
Stark K, Vainio S, Vassileva G, McMahon A . Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature. 1994; 372(6507):679-83. DOI: 10.1038/372679a0. View

3.
Ferrari S, Traianedes K, Thorne M, Lafage-Proust M, Genever P, Cecchini M . A role for N-cadherin in the development of the differentiated osteoblastic phenotype. J Bone Miner Res. 2000; 15(2):198-208. DOI: 10.1359/jbmr.2000.15.2.198. View

4.
Stewart S, Stankunas K . Limited dedifferentiation provides replacement tissue during zebrafish fin regeneration. Dev Biol. 2012; 365(2):339-49. PMC: 3370987. DOI: 10.1016/j.ydbio.2012.02.031. View

5.
Izu Y, Sun M, Zwolanek D, Veit G, Williams V, Cha B . Type XII collagen regulates osteoblast polarity and communication during bone formation. J Cell Biol. 2011; 193(6):1115-30. PMC: 3115787. DOI: 10.1083/jcb.201010010. View