Yeung Joanna, Goldowitz Daniel
Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, 950 West 28th Avenue, Vancouver, BC V5Z 4H4, Canada.
Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, 950 West 28th Avenue, Vancouver, BC V5Z 4H4, Canada.
Neuroscience. 2017 Jun 23;354:30-42. doi: 10.1016/j.neuroscience.2017.04.020. Epub 2017 Apr 24.
Wntless (Wls) is implicated in the Wnt signaling pathway by regulating the secretion of Wnt molecules. During brain development, Wls is expressed in the isthmic organizer (ISO) and rhombic lip (RL). Wls regulates Wnt1 secretion at the ISO which is required to induce midbrain-hindbrain structures. However, Wls function in the RL is not known. Here, we employed Nestin-cre to delete Wls specifically in the RL during mid-gestation. The loss-of-Wls leads to an abnormal RL during development and cerebellar vermis hypoplasia at birth. The Wls conditional knockout (cKO) has rudimentary foliation with an absence of Bergmann glia fibers in the external germinal layer (EGL). The Wls-cKO cerebellum also exhibits ectopia of several cell types and aberrations in granule cell organization. Finally, there is a loss of 85% of unipolar brush cells. From these findings, Wls-expressing cells in the rhombic lip are implicated in the orchestration of cerebellar development.
无翅型MMTV整合位点家族成员(Wntless,Wls)通过调节Wnt分子的分泌参与Wnt信号通路。在脑发育过程中,Wls在峡部组织者(ISO)和菱唇(RL)中表达。Wls在ISO调节Wnt1的分泌,这是诱导中脑 - 后脑结构所必需的。然而,Wls在RL中的功能尚不清楚。在这里,我们利用Nestin - cre在妊娠中期特异性删除RL中的Wls。Wls的缺失导致发育过程中RL异常以及出生时小脑蚓部发育不全。Wls条件性敲除(cKO)的小脑叶形成基本发育不全,外颗粒层(EGL)中缺乏伯格曼胶质纤维。Wls - cKO小脑还表现出几种细胞类型的异位和颗粒细胞组织异常。最后,单极刷细胞减少了85%。从这些发现来看,菱唇中表达Wls的细胞参与了小脑发育的调控。