Forge Andrew, Taylor Ruth R, Dawson Sally J, Lovett Michael, Jagger Daniel J
UCL Ear Institute, University College London, London, United Kingdom.
National Heart and Lung Institute, Imperial College London, London, United Kingdom.
PLoS Genet. 2017 Mar 27;13(3):e1006692. doi: 10.1371/journal.pgen.1006692. eCollection 2017 Mar.
Behavioural anomalies suggesting an inner ear disorder were observed in a colony of transgenic mice. Affected animals were profoundly deaf. Severe hair bundle defects were identified in all outer and inner hair cells (OHC, IHC) in the cochlea and in hair cells of vestibular macular organs, but hair cells in cristae were essentially unaffected. Evidence suggested the disorder was likely due to gene disruption by a randomly inserted transgene construct. Whole-genome sequencing identified interruption of the SorCS2 (Sortilin-related VPS-10 domain containing protein) locus. Real-time-qPCR demonstrated disrupted expression of SorCS2 RNA in cochlear tissue from affected mice and this was confirmed by SorCS2 immuno-labelling. In all affected hair cells, stereocilia were shorter than normal, but abnormalities of bundle morphology and organisation differed between hair cell types. Bundles on OHC were grossly misshapen with significantly fewer stereocilia than normal. However, stereocilia were organised in rows of increasing height. Bundles on IHC contained significantly more stereocilia than normal with some longer stereocilia towards the centre, or with minimal height differentials. In early postnatal mice, kinocilia (primary cilia) of IHC and of OHC were initially located towards the lateral edge of the hair cell surface but often became surrounded by stereocilia as bundle shape and apical surface contour changed. In macular organs the kinocilium was positioned in the centre of the cell surface throughout maturation. There was disruption of the signalling pathway controlling intrinsic hair cell apical asymmetry. LGN and Gαi3 were largely absent, and atypical Protein Kinase C (aPKC) lost its asymmetric distribution. The results suggest that SorCS2 plays a role upstream of the intrinsic polarity pathway and that there are differences between hair cell types in the deployment of the machinery that generates a precisely organised hair bundle.
在一群转基因小鼠中观察到了提示内耳疾病的行为异常。受影响的动物完全失聪。在耳蜗的所有外毛细胞和内毛细胞(OHC、IHC)以及前庭黄斑器官的毛细胞中都发现了严重的毛束缺陷,但嵴中的毛细胞基本未受影响。有证据表明,这种疾病可能是由于随机插入的转基因构建体导致基因破坏所致。全基因组测序确定了SorCS2(含Sortilin相关VPS - 10结构域蛋白)基因座的中断。实时定量PCR证明受影响小鼠耳蜗组织中SorCS2 RNA的表达受到破坏,这通过SorCS2免疫标记得到证实。在所有受影响的毛细胞中,静纤毛比正常的短,但毛束形态和组织的异常在不同类型的毛细胞之间存在差异。OHC上的毛束严重畸形,静纤毛比正常的明显少。然而,静纤毛按高度递增排列成行。IHC上的毛束含有比正常明显更多的静纤毛,一些较长的静纤毛朝向中心,或者高度差异最小。在出生后早期的小鼠中,IHC和OHC的动纤毛(初级纤毛)最初位于毛细胞表面的外侧边缘,但随着毛束形状和顶端表面轮廓的变化,它们常常被静纤毛包围。在黄斑器官中,动纤毛在整个成熟过程中都位于细胞表面的中心。控制毛细胞内在顶端不对称性的信号通路受到破坏。LGN和Gαi3基本缺失,非典型蛋白激酶C(aPKC)失去了不对称分布。结果表明,SorCS2在内在极性通路的上游发挥作用,并且在产生精确组织的毛束的机制的部署中,不同类型的毛细胞之间存在差异。