Journal article

Intranasal administration of mesenchymoangioblast-derived mesenchymal stem cells abrogates airway fibrosis and airway hyperresponsiveness associated with chronic allergic airways disease

Simon G Royce, Siddharth Rele, Brad RS Broughton, Kilian Kelly, Chrishan S Samuel

FASEB JOURNAL | FEDERATION AMER SOC EXP BIOL | Published : 2017

Abstract

Structural changes known as airway remodeling (AWR) characterize chronic/severe asthma and contribute to lung dysfunction. Thus, we assessed the in vivo efficacy of induced pluripotent stem cell and mesenchymoangioblast-derived mesenchymal stem cells (MCA-MSCs) on AWR in a murine model of chronic allergic airways disease (AAD)/asthma. Female Balb/c mice were subjected to a 9-wk model of ovalbumin (Ova)-induced chronic AAD and treated intravenously or intranasally with MCA-MSCs from weeks 9 to 11. Changes in airway inflammation (AI), AWR, and airway hyperresponsiveness (AHR) were assessed. Ova-injured mice presented with AI, goblet cell metaplasia, epithelial thickening, increased airway TGF-..

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Grants

Awarded by National Health and Medical Research Council (NHMRC) of Australia


Funding Acknowledgements

The authors acknowledge the facilities and technical assistance of Monash Histology Platform (Department of Anatomy and Developmental Biology, Monash University). This work was supported by a National Health and Medical Research Council (NHMRC) of Australia Senior Research Fellowship (GNT1041766) to C.S.S., and by Cynata Therapeutics funding to C.S.S. and S.G.R. S.G.R., S.R., B.R.S.B., and C.S.S. are with the Cardiovascular Disease Program, Biomedicine Discovery Institute and Department of Pharmacology, Monash University. S.G.R. is also affiliated with the Central Clinical School, Monash University. K.K. is an employee and shareholder of Cynata Therapeutics Ltd., but was not involved with performing the experiments or analysis of data.