Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus

© AlphaMed Press 2015. Airway epithelial cells generated from pluripotent stem cells (PSCs) represent a resource for research into a variety of human respiratory conditions, including those resulting from infection with common human pathogens. Using an NKX2.1-GFP reporter humanembryonic stem cell li...

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Main Authors: Jenny, R.A., Hirst, C., Lim, S.M., Goulburn, A.L., Micallef, S.J., Labonne, T., Kicic, Anthony, Ling, K.M., Stick, S.M., Ng, E.S., Trounson, A., Giudice, A., Elefanty, A.G., Stanley, E.G.
Format: Journal Article
Language:English
Published: ALPHAMED PRESS 2015
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/76816
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author Jenny, R.A.
Hirst, C.
Lim, S.M.
Goulburn, A.L.
Micallef, S.J.
Labonne, T.
Kicic, Anthony
Ling, K.M.
Stick, S.M.
Ng, E.S.
Trounson, A.
Giudice, A.
Elefanty, A.G.
Stanley, E.G.
author_facet Jenny, R.A.
Hirst, C.
Lim, S.M.
Goulburn, A.L.
Micallef, S.J.
Labonne, T.
Kicic, Anthony
Ling, K.M.
Stick, S.M.
Ng, E.S.
Trounson, A.
Giudice, A.
Elefanty, A.G.
Stanley, E.G.
author_sort Jenny, R.A.
building Curtin Institutional Repository
collection Online Access
description © AlphaMed Press 2015. Airway epithelial cells generated from pluripotent stem cells (PSCs) represent a resource for research into a variety of human respiratory conditions, including those resulting from infection with common human pathogens. Using an NKX2.1-GFP reporter humanembryonic stem cell line, wede-veloped a serum-free protocol for the generation of NKX2.1 < sup > + < /sup > endoderm that, when transplanted into immunodeficient mice, matured into respiratory cell types identified by expression of CC10, MUC5AC, and surfactant proteins. Gene profiling experiments indicated that day 10 NKX2.1 < sup > + < /sup > endo-derm expressed markers indicative of early foregut but lacked genes associated with later stages of respiratory epithelial cell differentiation. Nevertheless, NKX2.1 < sup > + < /sup > endoderm supported the infection and replication of the common respiratory pathogen human rhinovirus HRV1b. Moreover, NKX2.1 < sup > + < /sup > endoderm upregulated expression of IL-6, IL-8, and IL-1B in response to infection, a characteristic of human airway epithelial cells. Our experiments provide proof of principle for the use of PSC-derived respiratory epithelial cells in the study of cell-virus interactions.
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spelling curtin-20.500.11937-768162019-11-12T06:06:08Z Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus Jenny, R.A. Hirst, C. Lim, S.M. Goulburn, A.L. Micallef, S.J. Labonne, T. Kicic, Anthony Ling, K.M. Stick, S.M. Ng, E.S. Trounson, A. Giudice, A. Elefanty, A.G. Stanley, E.G. Science & Technology Life Sciences & Biomedicine Cell & Tissue Engineering Cell Biology Human embryonic stem cells NKX2.1 Respiratory endoderm Lung HRV Differentiation Rhinovirus GFP ANTERIOR FOREGUT ENDODERM TRANSCRIPTION FACTOR-I PDGF RECEPTOR-ALPHA DIRECTED DIFFERENTIATION DEFINITIVE ENDODERM LUNG MORPHOGENESIS PRIMITIVE STREAK AIRWAY EPITHELIA CYSTIC-FIBROSIS VITRO MODEL © AlphaMed Press 2015. Airway epithelial cells generated from pluripotent stem cells (PSCs) represent a resource for research into a variety of human respiratory conditions, including those resulting from infection with common human pathogens. Using an NKX2.1-GFP reporter humanembryonic stem cell line, wede-veloped a serum-free protocol for the generation of NKX2.1 < sup > + < /sup > endoderm that, when transplanted into immunodeficient mice, matured into respiratory cell types identified by expression of CC10, MUC5AC, and surfactant proteins. Gene profiling experiments indicated that day 10 NKX2.1 < sup > + < /sup > endo-derm expressed markers indicative of early foregut but lacked genes associated with later stages of respiratory epithelial cell differentiation. Nevertheless, NKX2.1 < sup > + < /sup > endoderm supported the infection and replication of the common respiratory pathogen human rhinovirus HRV1b. Moreover, NKX2.1 < sup > + < /sup > endoderm upregulated expression of IL-6, IL-8, and IL-1B in response to infection, a characteristic of human airway epithelial cells. Our experiments provide proof of principle for the use of PSC-derived respiratory epithelial cells in the study of cell-virus interactions. 2015 Journal Article http://hdl.handle.net/20.500.11937/76816 10.5966/sctm.2014-0274 English ALPHAMED PRESS restricted
spellingShingle Science & Technology
Life Sciences & Biomedicine
Cell & Tissue Engineering
Cell Biology
Human embryonic stem cells
NKX2.1
Respiratory endoderm
Lung
HRV
Differentiation
Rhinovirus
GFP
ANTERIOR FOREGUT ENDODERM
TRANSCRIPTION FACTOR-I
PDGF RECEPTOR-ALPHA
DIRECTED DIFFERENTIATION
DEFINITIVE ENDODERM
LUNG MORPHOGENESIS
PRIMITIVE STREAK
AIRWAY EPITHELIA
CYSTIC-FIBROSIS
VITRO MODEL
Jenny, R.A.
Hirst, C.
Lim, S.M.
Goulburn, A.L.
Micallef, S.J.
Labonne, T.
Kicic, Anthony
Ling, K.M.
Stick, S.M.
Ng, E.S.
Trounson, A.
Giudice, A.
Elefanty, A.G.
Stanley, E.G.
Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus
title Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus
title_full Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus
title_fullStr Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus
title_full_unstemmed Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus
title_short Productive infection of human embryonic stem cell-derived NKX2.1+ respiratory progenitors with human rhinovirus
title_sort productive infection of human embryonic stem cell-derived nkx2.1+ respiratory progenitors with human rhinovirus
topic Science & Technology
Life Sciences & Biomedicine
Cell & Tissue Engineering
Cell Biology
Human embryonic stem cells
NKX2.1
Respiratory endoderm
Lung
HRV
Differentiation
Rhinovirus
GFP
ANTERIOR FOREGUT ENDODERM
TRANSCRIPTION FACTOR-I
PDGF RECEPTOR-ALPHA
DIRECTED DIFFERENTIATION
DEFINITIVE ENDODERM
LUNG MORPHOGENESIS
PRIMITIVE STREAK
AIRWAY EPITHELIA
CYSTIC-FIBROSIS
VITRO MODEL
url http://hdl.handle.net/20.500.11937/76816