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  • Poster presentation
  • Open Access

Towards gene therapy for primary ciliary dyskinesia

Cilia20121 (Suppl 1) :P109

https://doi.org/10.1186/2046-2530-1-S1-P109

  • Published:

Keywords

  • Gene Therapy
  • Human Bronchial Epithelial Cell
  • Primary Ciliary Dyskinesia
  • Mammalian Expression Vector
  • Rare Genetic Disorder

Primary ciliary dyskinesia (PCD) describes a family of rare genetic disorders affecting ciliary motility in several organ systems. The respiratory defects that can lead to lung failure, however, are most concerning. New treatments for PCD are needed that prevent progressive lung damage and we aim to develop gene therapy to achieve this. DNAH5 is the gene most frequently mutated in PCD. It encodes a large 500kDa structural protein with ATPase activity that powers ciliary movement. PCD rarity, the shortage of genotyped patient samples and lack of suitable animal models means that better model systems are needed in which to study gene therapies. A further challenge is that gene transfer of DNAH5 will require an efficient non-viral delivery vector capable of packaging this gene, which is too large for commonly used viral vectors. To model PCD we have used RNA interference to silence DNAH5 in normal human bronchial epithelial cells grown in air-liquid interface cultures. Cells were transduced with a lentivirus expressing an shRNA for DNAH5. Silencing of DNAH5 expression was demonstrated and preliminary evidence that the cilia were immotile. We have cloned DNAH5 from mRNA of human ciliated cells into a mammalian expression vector and sequenced it. The DNAH5 clone expressed both mRNA and protein in transfected cells. Transfections were performed with a nanocomplex formulation comprising liposomes and targeting peptides that we have developed for DNAH5 gene transfer to the respiratory epithelium. We are now able to investigate PCD gene therapy using these models, DNAH5 constructs and vector delivery system.

Authors’ Affiliations

(1)
UCL Institute of Child Health, UK
(2)
University of Leicester, UK

Copyright

© Munye et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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