Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia
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...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-08-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/22/16/8361 |
id |
doaj-2216c5080482403cba47ae664b51ca19 |
---|---|
record_format |
Article |
spelling |
doaj-2216c5080482403cba47ae664b51ca192021-08-26T13:51:06ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-08-01228361836110.3390/ijms22168361Zebrafish Motile Cilia as a Model for Primary Ciliary DyskinesiaAndreia L. Pinto0Margarida Rasteiro1Catarina Bota2Sara Pestana3Pedro Sampaio4Claire Hogg5Thomas Burgoyne6Susana S. Lopes7Paediatric Respiratory Medicine, Primary Ciliary Dyskinesia Centre, Royal Brompton & Harefield NHS Trust, London SW3 6NP, UKCEDOC, NOVA Medical School, Rua Câmara Pestana nº 6, 6-A, Edifício CEDOC II, 1150-082 Lisboa, PortugalCEDOC, NOVA Medical School, Rua Câmara Pestana nº 6, 6-A, Edifício CEDOC II, 1150-082 Lisboa, PortugalCEDOC, NOVA Medical School, Rua Câmara Pestana nº 6, 6-A, Edifício CEDOC II, 1150-082 Lisboa, PortugalCEDOC, NOVA Medical School, Rua Câmara Pestana nº 6, 6-A, Edifício CEDOC II, 1150-082 Lisboa, PortugalPaediatric Respiratory Medicine, Primary Ciliary Dyskinesia Centre, Royal Brompton & Harefield NHS Trust, London SW3 6NP, UKPaediatric Respiratory Medicine, Primary Ciliary Dyskinesia Centre, Royal Brompton & Harefield NHS Trust, London SW3 6NP, UKCEDOC, NOVA Medical School, Rua Câmara Pestana nº 6, 6-A, Edifício CEDOC II, 1150-082 Lisboa, PortugalZebrafish 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.https://www.mdpi.com/1422-0067/22/16/8361transmission electron microscopymotile cilialeft–right organizerolfactory pitelectron tomographyanimal model |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andreia L. Pinto Margarida Rasteiro Catarina Bota Sara Pestana Pedro Sampaio Claire Hogg Thomas Burgoyne Susana S. Lopes |
spellingShingle |
Andreia L. Pinto Margarida Rasteiro Catarina Bota Sara Pestana Pedro Sampaio Claire Hogg Thomas Burgoyne Susana S. Lopes Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia International Journal of Molecular Sciences transmission electron microscopy motile cilia left–right organizer olfactory pit electron tomography animal model |
author_facet |
Andreia L. Pinto Margarida Rasteiro Catarina Bota Sara Pestana Pedro Sampaio Claire Hogg Thomas Burgoyne Susana S. Lopes |
author_sort |
Andreia L. Pinto |
title |
Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia |
title_short |
Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia |
title_full |
Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia |
title_fullStr |
Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia |
title_full_unstemmed |
Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia |
title_sort |
zebrafish motile cilia as a model for primary ciliary dyskinesia |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2021-08-01 |
description |
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. |
topic |
transmission electron microscopy motile cilia left–right organizer olfactory pit electron tomography animal model |
url |
https://www.mdpi.com/1422-0067/22/16/8361 |
work_keys_str_mv |
AT andreialpinto zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT margaridarasteiro zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT catarinabota zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT sarapestana zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT pedrosampaio zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT clairehogg zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT thomasburgoyne zebrafishmotileciliaasamodelforprimaryciliarydyskinesia AT susanaslopes zebrafishmotileciliaasamodelforprimaryciliarydyskinesia |
_version_ |
1721192671093981184 |