Macrophage Wnt7b is critical for kidney repair and regeneration

Shuei‐Liong Lin(Brigham and Women's Hospital), Bing Li(Brigham and Women's Hospital), Sujata Rao(Cincinnati Children's Hospital Medical Center), Eun-Jin Yeo(Cincinnati Children's Hospital Medical Center), Thomas E. Hudson(Brigham and Women's Hospital), Brian T. Nowlin(Brigham and Women's Hospital), Huaying Pei(Brigham and Women's Hospital), Lijun Chen(St. Jude Children's Research Hospital), Jie Zheng(St. Jude Children's Research Hospital), Thomas J. Carroll(The University of Texas Southwestern Medical Center), Jeffrey W. Pollard(Albert Einstein College of Medicine), Andrew P. McMahon(Harvard University), Richard A. Lang(Cincinnati Children's Hospital Medical Center), Jeremy S. Duffield(Brigham and Women's Hospital)
Proceedings of the National Academy of Sciences
February 16, 2010
Cited by 421Open Access
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Abstract

Macrophages are required for tissue homeostasis through their role in regulation of the immune response and the resolution of injury. Here we show, using the kidney as a model, that the Wnt pathway ligand Wnt7b is produced by macrophages to stimulate repair and regeneration. When macrophages are inducibly ablated from the injured kidney, the canonical Wnt pathway response in kidney epithelial cells is reduced. Furthermore, when Wnt7b is somatically deleted in macrophages, repair of injury is greatly diminished. Finally, injection of the Wnt pathway regulator Dkk2 enhances the repair process and suggests a therapeutic option. Because Wnt7b is known to stimulate epithelial responses during kidney development, these findings suggest that macrophages are able to rapidly invade an injured tissue and reestablish a developmental program that is beneficial for repair and regeneration.


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