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纤毛在协调晶状体纤维精确排列中起非必需作用。

Non-essential role for cilia in coordinating precise alignment of lens fibres.

作者信息

Sugiyama Yuki, Shelley Elizabeth J, Yoder Bradley K, Kozmik Zbynek, May-Simera Helen L, Beales Philip L, Lovicu Frank J, McAvoy John W

机构信息

Save Sight Institute, The University of Sydney, Sydney, NSW 2000, Australia.

Save Sight Institute, The University of Sydney, Sydney, NSW 2000, Australia.

出版信息

Mech Dev. 2016 Feb;139:10-7. doi: 10.1016/j.mod.2016.01.003. Epub 2016 Jan 26.

Abstract

The primary cilium, a microtubule-based organelle found in most cells, is a centre for mechano-sensing fluid movement and cellular signalling, notably through the Hedgehog pathway. We recently found that each lens fibre cell has an apically situated primary cilium that is polarised to the side of the cell facing the anterior pole of the lens. The direction of polarity is similar in neighbouring cells so that in the global view, lens fibres exhibit planar cell polarity (PCP) along the equatorial-anterior polar axis. Ciliogenesis has been associated with the establishment of PCP, although the exact relationship between PCP and the role of cilia is still controversial. To test the hypothesis that the primary cilia have a role in coordinating the precise alignment/orientation of the fibre cells, IFT88, a key component of the intraflagellar transport (IFT) complex, was removed specifically from the lens at different developmental stages using several lens-specific Cre-expressing mouse lines (MLR10- and LR-Cre). Irrespective of which Cre-line was adopted, both demonstrated that in IFT88-depleted cells, the ciliary axoneme was absent or substantially shortened, confirming the disruption of primary cilia formation. However no obvious histological defects were detected even when IFT88 was removed from the lens placode as early as E9.5. Specifically, the lens fibres aligned/oriented towards the poles to form the characteristic Y-shaped sutures as normal. Consistent with this, in primary lens epithelial explants prepared from these conditional knockout mouse lenses, the basal bodies still showed polarised localisation at the apical surface of elongating cells upon FGF-induced fibre differentiation. We further investigated the lens phenotype in knockouts of Bardet-Biedl Syndrome (BBS) proteins 4 and 8, the components of the BBSome complex which modulate ciliary function. In these BBS4 and 8 knockout lenses, again we found the pattern of the anterior sutures formed by the apical tips of elongating/migrating fibres were comparable to the control lenses. Taken together, these results indicate that primary cilia do not play an essential role in the precise cellular alignment/orientation of fibre cells. Thus, it appears that in the lens cilia are not required to establish PCP.

摘要

初级纤毛是一种存在于大多数细胞中的基于微管的细胞器,是机械感知流体流动和细胞信号传导的中心,特别是通过刺猬信号通路。我们最近发现,每个晶状体纤维细胞都有一个位于顶端的初级纤毛,其极性朝向细胞面向晶状体前极的一侧。相邻细胞的极性方向相似,因此从整体来看,晶状体纤维沿赤道 - 前极轴呈现平面细胞极性(PCP)。纤毛发生与PCP的建立有关,尽管PCP与纤毛作用的确切关系仍存在争议。为了验证初级纤毛在协调纤维细胞的精确排列/定向中起作用的假设,使用几种晶状体特异性表达Cre的小鼠品系(MLR10 - 和LR - Cre)在不同发育阶段从晶状体中特异性去除鞭毛内运输(IFT)复合体的关键成分IFT88。无论采用哪种Cre品系,两者都表明在IFT88缺失的细胞中,睫状轴丝不存在或显著缩短,证实了初级纤毛形成的破坏。然而,即使早在E9.5时就从晶状体基板中去除IFT88,也未检测到明显的组织学缺陷。具体而言,晶状体纤维正常地向两极排列/定向以形成特征性的Y形缝合线。与此一致的是,在从这些条件性敲除小鼠晶状体制备的原代晶状体上皮外植体中,在FGF诱导的纤维分化时,基体仍在伸长细胞的顶端表面显示出极性定位。我们进一步研究了巴德 - 比德尔综合征(BBS)蛋白4和8基因敲除小鼠的晶状体表型,BBS蛋白4和8是调节纤毛功能的BBSome复合体的组成部分。在这些BBS4和8基因敲除的晶状体中,我们再次发现由伸长/迁移纤维的顶端形成的前缝合线模式与对照晶状体相当。综上所述,这些结果表明初级纤毛在纤维细胞的精确细胞排列/定向中不发挥重要作用。因此,似乎在晶状体中建立PCP不需要纤毛。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a553/4789115/c6aac84aea43/nihms756674f1.jpg

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