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Article: Epigenetic regulation in B-cell maturation and its dysregulation in autoimmunity

TitleEpigenetic regulation in B-cell maturation and its dysregulation in autoimmunity
Authors
KeywordsAutoimmunity
B cell
DNA methylation
Histone modification
MicroRNA
Issue Date2018
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/cmi/index.html
Citation
Cellular & Molecular Immunology, 2018, v. 15 n. 7, p. 676-684 How to Cite?
AbstractB cells have a critical role in the initiation and acceleration of autoimmune diseases, especially those mediated by autoantibodies. In the peripheral lymphoid system, mature B cells are activated by self or/and foreign antigens and signals from helper T cells for differentiating into either memory B cells or antibody-producing plasma cells. Accumulating evidence has shown that epigenetic regulations modulate somatic hypermutation and class switch DNA recombination during B-cell activation and differentiation. Any abnormalities in these complex regulatory processes may contribute to aberrant antibody production, resulting in autoimmune pathogenesis such as systemic lupus erythematosus. Newly generated knowledge from advanced modern technologies such as next-generation sequencing, single-cell sequencing and DNA methylation sequencing has enabled us to better understand B-cell biology and its role in autoimmune development. Thus this review aims to summarize current research progress in epigenetic modifications contributing to B-cell activation and differentiation, especially under autoimmune conditions such as lupus, rheumatoid arthritis and type 1 diabetes.
Persistent Identifierhttp://hdl.handle.net/10722/262541
ISSN
2023 Impact Factor: 21.8
2023 SCImago Journal Rankings: 4.838
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWu, H-
dc.contributor.authorDeng, Y-
dc.contributor.authorFeng, Y-
dc.contributor.authorLong, D-
dc.contributor.authorMa, K-
dc.contributor.authorWang, X-
dc.contributor.authorZhao, M-
dc.contributor.authorLu, L-
dc.contributor.authorLu, Q-
dc.date.accessioned2018-09-28T05:01:05Z-
dc.date.available2018-09-28T05:01:05Z-
dc.date.issued2018-
dc.identifier.citationCellular & Molecular Immunology, 2018, v. 15 n. 7, p. 676-684-
dc.identifier.issn1672-7681-
dc.identifier.urihttp://hdl.handle.net/10722/262541-
dc.description.abstractB cells have a critical role in the initiation and acceleration of autoimmune diseases, especially those mediated by autoantibodies. In the peripheral lymphoid system, mature B cells are activated by self or/and foreign antigens and signals from helper T cells for differentiating into either memory B cells or antibody-producing plasma cells. Accumulating evidence has shown that epigenetic regulations modulate somatic hypermutation and class switch DNA recombination during B-cell activation and differentiation. Any abnormalities in these complex regulatory processes may contribute to aberrant antibody production, resulting in autoimmune pathogenesis such as systemic lupus erythematosus. Newly generated knowledge from advanced modern technologies such as next-generation sequencing, single-cell sequencing and DNA methylation sequencing has enabled us to better understand B-cell biology and its role in autoimmune development. Thus this review aims to summarize current research progress in epigenetic modifications contributing to B-cell activation and differentiation, especially under autoimmune conditions such as lupus, rheumatoid arthritis and type 1 diabetes.-
dc.languageeng-
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/cmi/index.html-
dc.relation.ispartofCellular & Molecular Immunology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAutoimmunity-
dc.subjectB cell-
dc.subjectDNA methylation-
dc.subjectHistone modification-
dc.subjectMicroRNA-
dc.titleEpigenetic regulation in B-cell maturation and its dysregulation in autoimmunity-
dc.typeArticle-
dc.identifier.emailMa, K: kongyang@hku.hk-
dc.identifier.emailWang, X: xhwangxh@hku.hk-
dc.identifier.emailLu, L: liweilu@hku.hk-
dc.identifier.authorityWang, X=rp02664-
dc.identifier.authorityLu, L=rp00477-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/cmi.2017.133-
dc.identifier.pmid29375128-
dc.identifier.pmcidPMC6123482-
dc.identifier.scopuseid_2-s2.0-85048595159-
dc.identifier.hkuros292477-
dc.identifier.volume15-
dc.identifier.issue7-
dc.identifier.spage676-
dc.identifier.epage684-
dc.identifier.isiWOS:000448426600007-
dc.publisher.placeChina-
dc.identifier.f1000732580127-
dc.identifier.issnl1672-7681-

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