Department of Biological Sciences, College of Information-Bio Convergence Engineering, Ulsan National Institute of Science and Technology, Ulsan, 44919, Republic of Korea.
Department of Biological Medical Engineering, College of Information-Bio Convergence Engineering, Ulsan National Institute of Science and Technology, Ulsan, 44919, Republic of Korea.
Genes Genomics. 2023 Feb;45(2):157-167. doi: 10.1007/s13258-022-01350-w. Epub 2022 Dec 12.
Motile cilia in a vertebrate are important to sustaining activities of life. Fluid flow on the apical surface of several tissues, including bronchial epithelium, ependymal epithelium, and fallopian tubules is generated by the ciliary beating of motile cilia. Multi-ciliated cells in ependymal tissue are responsible for the circulation of cerebrospinal fluid (CSF), which is essential for the development and homeostasis of the central nervous system, and airway tissues are protected from external contaminants by cilia-driven mucosal flow over the top of the airway epithelium.
A previous study reported that reduction of Ribc2 protein leads to disruption of ciliary beating in multi-ciliated cells. However, knowledge regarding the molecular function of Ribc2 is limited, thus currently available information is also limited. Therefore, we evaluated the importance of proteins involved in the interaction with Ribc2 in the process of ciliary beating.
Immunoprecipitation and mass spectrometry analysis was performed for the discovery of proteins involved in the interaction with Ribc2. Expression of the target gene was inhibited by injection of antisense morpholinos and measurement of the fluid flow on the embryonic epidermis of Xenopus was performed using fluorescent beads for examination of the ciliary beating of multi cilia. In addition, the flag-tagged protein was expressed by injection of mRNA and the changes in protein localization in the cilia were measured by immunostaining and western blot analysis for analysis of the molecular interaction between Ribc2 and Ribc2 binding proteins in multi-cilia.
The IP/MS analysis identified Ckb and Ybx2 as Ribc2 binding proteins and our results showed that localization of both Ckb and Ybx2 occurs at the axoneme of multi-cilia on the embryonic epithelium of Xenopus laevis. In addition, our findings confirmed that knock-down of Ckb or Ybx2 resulted in abnormal ciliary beating and reduction of cilia-driven fluid flow on multi-cilia of Xenopus laevis. In addition, significantly decreased localization of Ckb or Ybx2 in the ciliary axoneme was observed in Ribc2-depleted multi-cilia.
Ckb and Ybx2 are involved in the interaction with Ribc2 and are necessary for the ciliary beating of multi-cilia.
脊椎动物的游动纤毛对于维持生命活动至关重要。几种组织(包括支气管上皮、室管膜上皮和输卵管)的顶表面的流体流动是由游动纤毛的纤毛搏动产生的。室管膜组织中的多纤毛细胞负责脑脊液(CSF)的循环,这对中枢神经系统的发育和稳态至关重要,气道组织通过纤毛驱动的黏膜在气道上皮上方流动来保护免受外部污染物的侵害。
先前的研究报告称,Ribc2 蛋白的减少会导致多纤毛细胞的纤毛搏动紊乱。然而,目前对 Ribc2 分子功能的了解有限,因此目前的可用信息也有限。因此,我们评估了参与与 Ribc2 相互作用的蛋白质在纤毛搏动过程中的重要性。
进行免疫沉淀和质谱分析以发现与 Ribc2 相互作用的蛋白质。通过注射反义形态发生素抑制靶基因的表达,并使用荧光珠测量 Xenopus 胚胎表皮上的流体流动,以检查多纤毛的纤毛搏动。此外,通过注射 mRNA 表达 Flag 标记的蛋白质,并通过免疫染色和 Western blot 分析测量纤毛中蛋白质定位的变化,以分析多纤毛中 Ribc2 与 Ribc2 结合蛋白之间的分子相互作用。
IP/MS 分析鉴定出 Ckb 和 Ybx2 是 Ribc2 结合蛋白,我们的结果表明 Ckb 和 Ybx2 的定位都发生在 Xenopus laevis 胚胎上皮的多纤毛轴突上。此外,我们的研究结果证实,Ckb 或 Ybx2 的敲低会导致多纤毛的纤毛搏动异常和纤毛驱动的流体流动减少。此外,在 Ribc2 耗尽的多纤毛中观察到 Ckb 或 Ybx2 在纤毛轴突中的定位显著减少。
Ckb 和 Ybx2 参与与 Ribc2 的相互作用,是多纤毛纤毛搏动所必需的。