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Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis
Objective. Recent advances in molecular techniques have revealed that there is bi-directional transfer of cells between mother and child during pregnancy, and the presence of a mother's cells in her child has been termed maternal microchimerism (MMc). There is the potential for maternal cells t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354676/ https://www.ncbi.nlm.nih.gov/pubmed/22271755 http://dx.doi.org/10.1093/rheumatology/ker430 |
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author | Ye, Yi van Zyl, Berendine Varsani, Hemlata Wedderburn, Lucy R. Ramanan, Athimalaipet Gillespie, Kathleen M. |
author_facet | Ye, Yi van Zyl, Berendine Varsani, Hemlata Wedderburn, Lucy R. Ramanan, Athimalaipet Gillespie, Kathleen M. |
author_sort | Ye, Yi |
collection | PubMed |
description | Objective. Recent advances in molecular techniques have revealed that there is bi-directional transfer of cells between mother and child during pregnancy, and the presence of a mother's cells in her child has been termed maternal microchimerism (MMc). There is the potential for maternal cells to provoke inappropriate immune responses in the child, which could be a factor in autoimmunity including JDM. The aim of this study was to determine whether maternal (female) cells could be detected in frozen muscle sections from seven males (age range 3–13 years) with JDM participating in the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory Myopathies and sections of muscle controls (age range 2–12 years). Methods. At least 1000 cells from each section underwent FISH and confocal imaging through each nucleus. Concomitant IF for CD45 was used to determine whether MMc in muscle were lymphocytes. A non-parametric Mann–Whitney U-test was used to detect statistical differences. Results. The frequency of MMc was higher in JDM muscle (0.42–1.14%) than in controls (0.08–0.42%) P = 0.01. No CD45(+) MMc were observed. Conclusion. These data confirm an increased frequency of MMc in JDM. More detailed characterization of MMc is required, particularly using phenotypic markers, to explain the role of these cells in JDM. |
format | Online Article Text |
id | pubmed-3354676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33546762012-05-17 Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis Ye, Yi van Zyl, Berendine Varsani, Hemlata Wedderburn, Lucy R. Ramanan, Athimalaipet Gillespie, Kathleen M. Rheumatology (Oxford) Basic Science Objective. Recent advances in molecular techniques have revealed that there is bi-directional transfer of cells between mother and child during pregnancy, and the presence of a mother's cells in her child has been termed maternal microchimerism (MMc). There is the potential for maternal cells to provoke inappropriate immune responses in the child, which could be a factor in autoimmunity including JDM. The aim of this study was to determine whether maternal (female) cells could be detected in frozen muscle sections from seven males (age range 3–13 years) with JDM participating in the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory Myopathies and sections of muscle controls (age range 2–12 years). Methods. At least 1000 cells from each section underwent FISH and confocal imaging through each nucleus. Concomitant IF for CD45 was used to determine whether MMc in muscle were lymphocytes. A non-parametric Mann–Whitney U-test was used to detect statistical differences. Results. The frequency of MMc was higher in JDM muscle (0.42–1.14%) than in controls (0.08–0.42%) P = 0.01. No CD45(+) MMc were observed. Conclusion. These data confirm an increased frequency of MMc in JDM. More detailed characterization of MMc is required, particularly using phenotypic markers, to explain the role of these cells in JDM. Oxford University Press 2012-06 2012-01-23 /pmc/articles/PMC3354676/ /pubmed/22271755 http://dx.doi.org/10.1093/rheumatology/ker430 Text en © The Author(s) 2012. Published by Oxford University Press on behalf of The British Society for Rheumatology. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Science Ye, Yi van Zyl, Berendine Varsani, Hemlata Wedderburn, Lucy R. Ramanan, Athimalaipet Gillespie, Kathleen M. Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
title | Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
title_full | Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
title_fullStr | Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
title_full_unstemmed | Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
title_short | Maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
title_sort | maternal microchimerism in muscle biopsies from children with juvenile dermatomyositis |
topic | Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354676/ https://www.ncbi.nlm.nih.gov/pubmed/22271755 http://dx.doi.org/10.1093/rheumatology/ker430 |
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