| Literature DB >> 28292423 |
Katsura Minegishi1, Masakazu Hashimoto2, Rieko Ajima3, Katsuyoshi Takaoka2, Kyosuke Shinohara2, Yayoi Ikawa4, Hiromi Nishimura4, Andrew P McMahon5, Karl Willert6, Yasushi Okada7, Hiroshi Sasaki8, Dongbo Shi9, Toshihiko Fujimori9, Toshihisa Ohtsuka10, Yasunobu Igarashi11, Terry P Yamaguchi12, Akihiko Shimono13, Hidetaka Shiratori2, Hiroshi Hamada14.
Abstract
Polarization of node cells along the anterior-posterior axis of mouse embryos is responsible for left-right symmetry breaking. How node cells become polarized has remained unknown, however. Wnt5a and Wnt5b are expressed posteriorly relative to the node, whereas genes for Sfrp inhibitors of Wnt signaling are expressed anteriorly. Here we show that polarization of node cells is impaired in Wnt5a-/-Wnt5b-/- and Sfrp mutant embryos, and also in the presence of a uniform distribution of Wnt5a or Sfrp1, suggesting that Wnt5 and Sfrp proteins act as instructive signals in this process. The absence of planar cell polarity (PCP) core proteins Prickle1 and Prickle2 in individual cells or local forced expression of Wnt5a perturbed polarization of neighboring wild-type cells. Our results suggest that opposing gradients of Wnt5a and Wnt5b and of their Sfrp inhibitors, together with intercellular signaling via PCP proteins, polarize node cells along the anterior-posterior axis for breaking of left-right symmetry.Entities:
Keywords: Sfrp; Wnt; basal body; breaking of left-right symmetry; cilia; planar cell polarity
Mesh:
Substances:
Year: 2017 PMID: 28292423 DOI: 10.1016/j.devcel.2017.02.010
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270