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From a gene-centric to whole-proteome view of differentiation of T helper cell subsets

Proper differentiation of naïve T helper cells into functionally distinct subsets is of critical importance to human health. Consequently, the process is tightly controlled by a complex intracellular signalling network. To dissect the regulatory principles of this network, immunologists have early o...

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Detalles Bibliográficos
Autores principales: Lönnberg, Tapio, Chen, Zhi, Lahesmaa, Riitta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3838199/
https://www.ncbi.nlm.nih.gov/pubmed/24106101
http://dx.doi.org/10.1093/bfgp/elt033
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author Lönnberg, Tapio
Chen, Zhi
Lahesmaa, Riitta
author_facet Lönnberg, Tapio
Chen, Zhi
Lahesmaa, Riitta
author_sort Lönnberg, Tapio
collection PubMed
description Proper differentiation of naïve T helper cells into functionally distinct subsets is of critical importance to human health. Consequently, the process is tightly controlled by a complex intracellular signalling network. To dissect the regulatory principles of this network, immunologists have early on embraced system-wide transcriptomics tools, leading to identification of large panels of potential regulatory factors. In contrast, the use of proteomics approaches in T helper cell research has been notably rare, and to this date relatively few high-throughput datasets have been reported. Here, we discuss the importance of such research and envision the possibilities afforded by mass spectrometry-based proteomics in the near future.
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spelling pubmed-38381992013-11-23 From a gene-centric to whole-proteome view of differentiation of T helper cell subsets Lönnberg, Tapio Chen, Zhi Lahesmaa, Riitta Brief Funct Genomics Papers Proper differentiation of naïve T helper cells into functionally distinct subsets is of critical importance to human health. Consequently, the process is tightly controlled by a complex intracellular signalling network. To dissect the regulatory principles of this network, immunologists have early on embraced system-wide transcriptomics tools, leading to identification of large panels of potential regulatory factors. In contrast, the use of proteomics approaches in T helper cell research has been notably rare, and to this date relatively few high-throughput datasets have been reported. Here, we discuss the importance of such research and envision the possibilities afforded by mass spectrometry-based proteomics in the near future. Oxford University Press 2013-11 2013-10-06 /pmc/articles/PMC3838199/ /pubmed/24106101 http://dx.doi.org/10.1093/bfgp/elt033 Text en © The Author 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Papers
Lönnberg, Tapio
Chen, Zhi
Lahesmaa, Riitta
From a gene-centric to whole-proteome view of differentiation of T helper cell subsets
title From a gene-centric to whole-proteome view of differentiation of T helper cell subsets
title_full From a gene-centric to whole-proteome view of differentiation of T helper cell subsets
title_fullStr From a gene-centric to whole-proteome view of differentiation of T helper cell subsets
title_full_unstemmed From a gene-centric to whole-proteome view of differentiation of T helper cell subsets
title_short From a gene-centric to whole-proteome view of differentiation of T helper cell subsets
title_sort from a gene-centric to whole-proteome view of differentiation of t helper cell subsets
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3838199/
https://www.ncbi.nlm.nih.gov/pubmed/24106101
http://dx.doi.org/10.1093/bfgp/elt033
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