Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.

Primary Ciliary Dyskinesia is a heterogeneous genetic disease that is characterized by cilia dysfunction of the epithelial cells lining the respiratory tracts, resulting in recurrent respiratory tract infections. Despite lifelong physiological therapy and antibiotics, the lungs of affected patients...

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Main Authors: Brigitte Chhin, Didier Negre, Olivier Merrot, Jacqueline Pham, Yves Tourneur, Denis Ressnikoff, Martine Jaspers, Mark Jorissen, François-Loïc Cosset, Patrice Bouvagnet
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-03-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC2650261?pdf=render
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spelling doaj-e8f41bd193c146f399e80d50febdcbf92020-11-25T02:01:10ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042009-03-0153e100042210.1371/journal.pgen.1000422Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.Brigitte ChhinDidier NegreOlivier MerrotJacqueline PhamYves TourneurDenis RessnikoffMartine JaspersMark JorissenFrançois-Loïc CossetPatrice BouvagnetPrimary Ciliary Dyskinesia is a heterogeneous genetic disease that is characterized by cilia dysfunction of the epithelial cells lining the respiratory tracts, resulting in recurrent respiratory tract infections. Despite lifelong physiological therapy and antibiotics, the lungs of affected patients are progressively destroyed, leading to respiratory insufficiency. Recessive mutations in Dynein Axonemal Intermediate chain type 1 (DNAI1) gene have been described in 10% of cases of Primary Ciliary Dyskinesia. Our goal was to restore normal ciliary beating in DNAI1-deficient human airway epithelial cells. A lentiviral vector based on Simian Immunodeficiency Virus pseudotyped with Vesicular Stomatitis Virus Glycoprotein was used to transduce cultured human airway epithelial cells with a cDNA of DNAI1 driven by the Elongation Factor 1 promoter. Transcription and translation of the transduced gene were tested by RT-PCR and western blot, respectively. Human airway epithelial cells that were DNAI1-deficient due to compound heterozygous mutations, and consequently had immotile cilia and no outer dynein arm, were transduced by the lentivirus. Cilia beating was recorded and electron microscopy of the cilia was performed. Transcription and translation of the transduced DNAI1 gene were detected in human cells treated with the lentivirus. In addition, immotile cilia recovered a normal beat and outer dynein arms reappeared. We demonstrated that it is possible to obtain a normalization of ciliary beat frequency of deficient human airway epithelial cells by using a lentivirus to transduce cells with the therapeutic gene. This preliminary step constitutes a conceptual proof that is indispensable in the perspective of Primary Ciliary Dyskinesia's in vivo gene therapy. This is the first time that recovery of cilia beating is demonstrated in this disease.http://europepmc.org/articles/PMC2650261?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Brigitte Chhin
Didier Negre
Olivier Merrot
Jacqueline Pham
Yves Tourneur
Denis Ressnikoff
Martine Jaspers
Mark Jorissen
François-Loïc Cosset
Patrice Bouvagnet
spellingShingle Brigitte Chhin
Didier Negre
Olivier Merrot
Jacqueline Pham
Yves Tourneur
Denis Ressnikoff
Martine Jaspers
Mark Jorissen
François-Loïc Cosset
Patrice Bouvagnet
Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
PLoS Genetics
author_facet Brigitte Chhin
Didier Negre
Olivier Merrot
Jacqueline Pham
Yves Tourneur
Denis Ressnikoff
Martine Jaspers
Mark Jorissen
François-Loïc Cosset
Patrice Bouvagnet
author_sort Brigitte Chhin
title Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
title_short Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
title_full Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
title_fullStr Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
title_full_unstemmed Ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
title_sort ciliary beating recovery in deficient human airway epithelial cells after lentivirus ex vivo gene therapy.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2009-03-01
description Primary Ciliary Dyskinesia is a heterogeneous genetic disease that is characterized by cilia dysfunction of the epithelial cells lining the respiratory tracts, resulting in recurrent respiratory tract infections. Despite lifelong physiological therapy and antibiotics, the lungs of affected patients are progressively destroyed, leading to respiratory insufficiency. Recessive mutations in Dynein Axonemal Intermediate chain type 1 (DNAI1) gene have been described in 10% of cases of Primary Ciliary Dyskinesia. Our goal was to restore normal ciliary beating in DNAI1-deficient human airway epithelial cells. A lentiviral vector based on Simian Immunodeficiency Virus pseudotyped with Vesicular Stomatitis Virus Glycoprotein was used to transduce cultured human airway epithelial cells with a cDNA of DNAI1 driven by the Elongation Factor 1 promoter. Transcription and translation of the transduced gene were tested by RT-PCR and western blot, respectively. Human airway epithelial cells that were DNAI1-deficient due to compound heterozygous mutations, and consequently had immotile cilia and no outer dynein arm, were transduced by the lentivirus. Cilia beating was recorded and electron microscopy of the cilia was performed. Transcription and translation of the transduced DNAI1 gene were detected in human cells treated with the lentivirus. In addition, immotile cilia recovered a normal beat and outer dynein arms reappeared. We demonstrated that it is possible to obtain a normalization of ciliary beat frequency of deficient human airway epithelial cells by using a lentivirus to transduce cells with the therapeutic gene. This preliminary step constitutes a conceptual proof that is indispensable in the perspective of Primary Ciliary Dyskinesia's in vivo gene therapy. This is the first time that recovery of cilia beating is demonstrated in this disease.
url http://europepmc.org/articles/PMC2650261?pdf=render
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