Ror‐family receptor tyrosine kinases in noncanonical Wnt signaling: Their implications in developmental morphogenesis and human diseases

Y Minami, I Oishi, M Endo… - … dynamics: an official …, 2010 - Wiley Online Library
Y Minami, I Oishi, M Endo, M Nishita
Developmental dynamics: an official publication of the American …, 2010Wiley Online Library
The Ror‐family receptor tyrosine kinases (RTKs) play crucial roles in the development of
various organs and tissues. In mammals, Ror2, a member of the Ror‐family RTKs, has been
shown to act as a receptor or coreceptor for Wnt5a to mediate noncanonical Wnt signaling.
Ror2‐and Wnt5a‐deficient mice exhibit similar abnormalities during developmental
morphogenesis, reflecting their defects in convergent extension movements and planar cell
polarity, characteristic features mediated by noncanonical Wnt signaling. Furthermore …
Abstract
The Ror‐family receptor tyrosine kinases (RTKs) play crucial roles in the development of various organs and tissues. In mammals, Ror2, a member of the Ror‐family RTKs, has been shown to act as a receptor or coreceptor for Wnt5a to mediate noncanonical Wnt signaling. Ror2‐ and Wnt5a‐deficient mice exhibit similar abnormalities during developmental morphogenesis, reflecting their defects in convergent extension movements and planar cell polarity, characteristic features mediated by noncanonical Wnt signaling. Furthermore, mutations within the human Ror2 gene are responsible for the genetic skeletal disorders dominant brachydactyly type B and recessive Robinow syndrome. Accumulating evidence demonstrate that Ror2 mediates noncanonical Wnt5a signaling by inhibiting the β‐catenin‐TCF pathway and activating the Wnt/JNK pathway that results in polarized cell migration. In this article, we review recent progress in understanding the roles of noncanonical Wnt5a/Ror2 signaling in developmental morphogenesis and in human diseases, including heritable skeletal disorders and tumor invasion. Developmental Dynamics 239:1–15, 2010. © 2009 Wiley‐Liss, Inc.
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