Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.

HLA class-I expression is weak in embryonic stem cells but increases rapidly during lineage progression. It is unknown whether all three classical HLA class-I antigens follow the same developmental program. In the present study, we investigated allele-specific expression of HLA-A, -B, and -C at the...

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Autores principales: Adiba Isa, Jan O Nehlin, Hardee J Sabir, Tom E Andersen, Michael Gaster, Moustapha Kassem, Torben Barington
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Publicado: Public Library of Science (PLoS) 2010
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Acceso en línea:https://doaj.org/article/78cf091d47624af88eee8f8156bd0a49
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spelling oai:doaj.org-article:78cf091d47624af88eee8f8156bd0a492021-12-02T20:21:16ZImpaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.1932-620310.1371/journal.pone.0010900https://doaj.org/article/78cf091d47624af88eee8f8156bd0a492010-05-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20531935/?tool=EBIhttps://doaj.org/toc/1932-6203HLA class-I expression is weak in embryonic stem cells but increases rapidly during lineage progression. It is unknown whether all three classical HLA class-I antigens follow the same developmental program. In the present study, we investigated allele-specific expression of HLA-A, -B, and -C at the mRNA and protein levels on human mesenchymal stem cells from bone marrow and adipose tissue as well as striated muscle satellite cells and lymphocytes. Using multicolour flow cytometry, we found high cell surface expression of HLA-A on all stem cells and PBMC examined. Surprisingly, HLA-B was either undetectable or very weakly expressed on all stem cells protecting them from complement-dependent cytotoxicity (CDC) using relevant human anti-B and anti-Cw sera. IFNgamma stimulation for 48-72 h was required to induce full HLA-B protein expression. Quantitative real-time RT-PCR showed that IFNgamma induced a 9-42 fold increase of all six HLA-A,-B,-C gene transcripts. Interestingly, prior to stimulation, gene transcripts for all but two alleles were present in similar amounts suggesting that post-transcriptional mechanisms regulate the constitutive expression of HLA-A,-B, and -C. Locus-restricted expression of HLA-A, -B and -C challenges our current understanding of the function of these molecules as regulators of CD8(+) T-cell and NK-cell function and should lead to further inquiries into their expression on other cell types.Adiba IsaJan O NehlinHardee J SabirTom E AndersenMichael GasterMoustapha KassemTorben BaringtonPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 5, p e10900 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Adiba Isa
Jan O Nehlin
Hardee J Sabir
Tom E Andersen
Michael Gaster
Moustapha Kassem
Torben Barington
Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.
description HLA class-I expression is weak in embryonic stem cells but increases rapidly during lineage progression. It is unknown whether all three classical HLA class-I antigens follow the same developmental program. In the present study, we investigated allele-specific expression of HLA-A, -B, and -C at the mRNA and protein levels on human mesenchymal stem cells from bone marrow and adipose tissue as well as striated muscle satellite cells and lymphocytes. Using multicolour flow cytometry, we found high cell surface expression of HLA-A on all stem cells and PBMC examined. Surprisingly, HLA-B was either undetectable or very weakly expressed on all stem cells protecting them from complement-dependent cytotoxicity (CDC) using relevant human anti-B and anti-Cw sera. IFNgamma stimulation for 48-72 h was required to induce full HLA-B protein expression. Quantitative real-time RT-PCR showed that IFNgamma induced a 9-42 fold increase of all six HLA-A,-B,-C gene transcripts. Interestingly, prior to stimulation, gene transcripts for all but two alleles were present in similar amounts suggesting that post-transcriptional mechanisms regulate the constitutive expression of HLA-A,-B, and -C. Locus-restricted expression of HLA-A, -B and -C challenges our current understanding of the function of these molecules as regulators of CD8(+) T-cell and NK-cell function and should lead to further inquiries into their expression on other cell types.
format article
author Adiba Isa
Jan O Nehlin
Hardee J Sabir
Tom E Andersen
Michael Gaster
Moustapha Kassem
Torben Barington
author_facet Adiba Isa
Jan O Nehlin
Hardee J Sabir
Tom E Andersen
Michael Gaster
Moustapha Kassem
Torben Barington
author_sort Adiba Isa
title Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.
title_short Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.
title_full Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.
title_fullStr Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.
title_full_unstemmed Impaired cell surface expression of HLA-B antigens on mesenchymal stem cells and muscle cell progenitors.
title_sort impaired cell surface expression of hla-b antigens on mesenchymal stem cells and muscle cell progenitors.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/78cf091d47624af88eee8f8156bd0a49
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