2.50
Hdl Handle:
http://hdl.handle.net/10547/604697
Title:
Tissue-derived hedgehog proteins modulate Th differentiation and disease
Authors:
Furmanski, Anna L.; Saldana, Jose Ignacio; Ono, Masahiro; Sahni, Hemant; Paschalidis, Nikolaos; D'Acquisto, Fulvio; Crompton, Tessa ( 0000-0002-8973-4021 )
Abstract:
Genome-wide association studies of complex immune-mediated diseases have indicated that many genetic factors, each with individual low risk, contribute to overall disease. It is therefore timely and important to characterize how immune responses may be subtly modified by tissue context. In this article, we explore the role of tissue-derived molecules in influencing the function of T cells, which, owing to their migratory nature, come into contact with many different microenvironments through their lifespan. Hedgehog (Hh) proteins act as secreted morphogens, providing concentration-dependent positional and temporal cell-fate specification in solid tissues. Hh signaling is required for embryogenesis and is important in postnatal tissue renewal and in malignancy. However, the function of Hh in dynamic, fluid systems, such as in mammalian immunity, is largely unknown. In this article, we show that Hh-dependent transcription in T cells promoted Th2 transcriptional programs and differentiation, exacerbating allergic disease. Of interest, expression of Sonic Hh increased in lung epithelial cells following the induction of allergic disease, and lung T cells upregulated Hh target gene expression, indicating that T cells respond to locally secreted Hh ligands in vivo. We show that Il4, the key Th2 cytokine, is a novel transcriptional target of Hh signals in T cells, providing one mechanism for the role of Hh in Th differentiation. We propose that Hh, secreted from inflamed, remodeling, or malignant tissue, can modulate local T cell function. Our data present an unexpected and novel role for tissue-derived morphogens in the regulation of fluid immune responses, with implications for allergy and tumor responses, suggesting new uses for anti-Hh therapeutics.
Affiliation:
University College London
Citation:
Furmanski AL, Saldana JI, Ono M, Sahni H, Paschalidis N, D'Acquisto F, Crompton T. (2013) 'Tissue-Derived Hedgehog Proteins Modulate Th Differentiation and Disease', The Journal of Immunology 190 (6):2641
Publisher:
American Association for Immunologists
Journal:
The Journal of Immunology
Issue Date:
13-Feb-2013
URI:
http://hdl.handle.net/10547/604697
DOI:
10.4049/jimmunol.1202541
PubMed ID:
23408837
PubMed Central ID:
PMC3672981
Additional Links:
http://www.jimmunol.org/cgi/doi/10.4049/jimmunol.1202541; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672981/
Type:
Article
Language:
en
ISSN:
0022-1767; 1550-6606
Sponsors:
This work was supported by the Wellcome Trust, the Biotechnology and Biological Sciences Research Council, and the Medical Research Council; A.L.F. is supported by Great Ormond Street Hospital/Institute of Child Health Biomedical Research Centre, funded by the Department of Health’s National Institute for Health Research’s Biomedical Research Centres scheme; M.O. by a Human Frontier Science Program Long Term Fellowship; and H.S. by a University College London Child Health Research Appeal Trust studentship.
Appears in Collections:
Biomedical Science

Full metadata record

DC FieldValue Language
dc.contributor.authorFurmanski, Anna L.en
dc.contributor.authorSaldana, Jose Ignacioen
dc.contributor.authorOno, Masahiroen
dc.contributor.authorSahni, Hemanten
dc.contributor.authorPaschalidis, Nikolaosen
dc.contributor.authorD'Acquisto, Fulvioen
dc.contributor.authorCrompton, Tessaen
dc.date.accessioned2016-04-07T08:54:21Zen
dc.date.available2016-04-07T08:54:21Zen
dc.date.issued2013-02-13en
dc.identifier.citationFurmanski AL, Saldana JI, Ono M, Sahni H, Paschalidis N, D'Acquisto F, Crompton T. (2013) 'Tissue-Derived Hedgehog Proteins Modulate Th Differentiation and Disease', The Journal of Immunology 190 (6):2641en
dc.identifier.issn0022-1767en
dc.identifier.issn1550-6606en
dc.identifier.pmid23408837en
dc.identifier.doi10.4049/jimmunol.1202541en
dc.identifier.urihttp://hdl.handle.net/10547/604697en
dc.description.abstractGenome-wide association studies of complex immune-mediated diseases have indicated that many genetic factors, each with individual low risk, contribute to overall disease. It is therefore timely and important to characterize how immune responses may be subtly modified by tissue context. In this article, we explore the role of tissue-derived molecules in influencing the function of T cells, which, owing to their migratory nature, come into contact with many different microenvironments through their lifespan. Hedgehog (Hh) proteins act as secreted morphogens, providing concentration-dependent positional and temporal cell-fate specification in solid tissues. Hh signaling is required for embryogenesis and is important in postnatal tissue renewal and in malignancy. However, the function of Hh in dynamic, fluid systems, such as in mammalian immunity, is largely unknown. In this article, we show that Hh-dependent transcription in T cells promoted Th2 transcriptional programs and differentiation, exacerbating allergic disease. Of interest, expression of Sonic Hh increased in lung epithelial cells following the induction of allergic disease, and lung T cells upregulated Hh target gene expression, indicating that T cells respond to locally secreted Hh ligands in vivo. We show that Il4, the key Th2 cytokine, is a novel transcriptional target of Hh signals in T cells, providing one mechanism for the role of Hh in Th differentiation. We propose that Hh, secreted from inflamed, remodeling, or malignant tissue, can modulate local T cell function. Our data present an unexpected and novel role for tissue-derived morphogens in the regulation of fluid immune responses, with implications for allergy and tumor responses, suggesting new uses for anti-Hh therapeutics.en
dc.description.sponsorshipThis work was supported by the Wellcome Trust, the Biotechnology and Biological Sciences Research Council, and the Medical Research Council; A.L.F. is supported by Great Ormond Street Hospital/Institute of Child Health Biomedical Research Centre, funded by the Department of Health’s National Institute for Health Research’s Biomedical Research Centres scheme; M.O. by a Human Frontier Science Program Long Term Fellowship; and H.S. by a University College London Child Health Research Appeal Trust studentship.en
dc.language.isoenen
dc.publisherAmerican Association for Immunologistsen
dc.relation.urlhttp://www.jimmunol.org/cgi/doi/10.4049/jimmunol.1202541en
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672981/en
dc.rightsArchived with thanks to The Journal of Immunologyen
dc.rightsAn error occurred on the license name.*
dc.rights.uriAn error occurred getting the license - uri.*
dc.subjecthedgehog proteinsen
dc.subjectC550 Immunologyen
dc.subjectTh differentiationen
dc.subjectT cellen
dc.titleTissue-derived hedgehog proteins modulate Th differentiation and diseaseen
dc.typeArticleen
dc.contributor.departmentUniversity College Londonen
dc.identifier.journalThe Journal of Immunologyen
dc.identifier.pmcidPMC3672981en

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