4.7 Article

Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia

期刊

出版社

MDPI
DOI: 10.3390/ijms22168361

关键词

transmission electron microscopy; motile cilia; left-right organizer; olfactory pit; electron tomography; animal model; zebrafish

资金

  1. European Union Horizon 2020 research and innovation [811087]
  2. Fundacao para a Ciencia e tecnologia [PTDC/BEX-BID/1411/2014, PD/BD/136927/2018, SFRH/BD/111611/2015, SFRH/BD/141034/2018]
  3. FCT CEEC-IND 2018
  4. Fundação para a Ciência e a Tecnologia [SFRH/BD/141034/2018, PD/BD/136927/2018, SFRH/BD/111611/2015, PTDC/BEX-BID/1411/2014] Funding Source: FCT

向作者/读者索取更多资源

Zebrafish, a widely used vertebrate teleost in research, presents unique advantages such as sustained transparency for at least 48 hours post fertilization. This study validates zebrafish motile cilia as organelles for Primary Ciliary Dyskinesia (PCD) research and characterizes different types of cilia in the olfactory pit and left-right organizer. The findings demonstrate the potential of zebrafish as a model organism for understanding human diseases and highlight the importance of considering specific physical differences for accurate interpretation of research results.
Zebrafish is a vertebrate teleost widely used in many areas of research. As embryos, they develop quickly and provide unique opportunities for research studies owing to their transparency for at least 48 h post fertilization. Zebrafish have many ciliated organs that include primary cilia as well as motile cilia. Using zebrafish as an animal model helps to better understand human diseases such as Primary Ciliary Dyskinesia (PCD), an autosomal recessive disorder that affects cilia motility, currently associated with more than 50 genes. The aim of this study was to validate zebrafish motile cilia, both in mono and multiciliated cells, as organelles for PCD research. For this purpose, we obtained systematic high-resolution data in both the olfactory pit (OP) and the left-right organizer (LRO), a superficial organ and a deep organ embedded in the tail of the embryo, respectively. For the analysis of their axonemal ciliary structure, we used conventional transmission electron microscopy (TEM) and electron tomography (ET). We characterised the wild-type OP cilia and showed, for the first time in zebrafish, the presence of motile cilia (9 + 2) in the periphery of the pit and the presence of immotile cilia (still 9 + 2), with absent outer dynein arms, in the centre of the pit. In addition, we reported that a central pair of microtubules in the LRO motile cilia is common in zebrafish, contrary to mouse embryos, but it is not observed in all LRO cilia from the same embryo. We further showed that the outer dynein arms of the microtubular doublet of both the OP and LRO cilia are structurally similar in dimensions to the human respiratory cilia at the resolution of TEM and ET. We conclude that zebrafish is a good model organism for PCD research but investigators need to be aware of the specific physical differences to correctly interpret their results.

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