Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription

Beside its classical role as a serum effector system of innate immunity, evidence is accumulating that complement has an intracellular repertoire of components that provides not only immune defense, but also functions to maintain cellular homeostasis. While complement proteins, mainly the central co...

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Main Authors: Mariann Kremlitzka, Alicja A. Nowacka, Frida C. Mohlin, Pradeep Bompada, Yang De Marinis, Anna M. Blom
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-03-01
Series:Frontiers in Immunology
Subjects:
DNA
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.00493/full
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spelling doaj-a0473d06864c4573af5b8e8eac0ce8332020-11-24T22:07:52ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-03-011010.3389/fimmu.2019.00493447094Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene TranscriptionMariann Kremlitzka0Alicja A. Nowacka1Frida C. Mohlin2Pradeep Bompada3Yang De Marinis4Anna M. Blom5Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, SwedenDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, SwedenDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, SwedenGenomics, Diabetes and Endocrinology, Department of Clinical Sciences Malmö, Lund University, Malmö, SwedenGenomics, Diabetes and Endocrinology, Department of Clinical Sciences Malmö, Lund University, Malmö, SwedenDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, SwedenBeside its classical role as a serum effector system of innate immunity, evidence is accumulating that complement has an intracellular repertoire of components that provides not only immune defense, but also functions to maintain cellular homeostasis. While complement proteins, mainly the central component C3, have been detected in B cells, their exact function and source remain largely unexplored. In this study, we investigated the expression and origin of intracellular C3 in human B cells together with its role in B cell homeostasis. Our data provide evidence that endogenous expression of C3 is very low in human B cells and, in accordance with the recent publication, the main origin of intracellular C3 is the serum. Interestingly, we found that both serum-derived and purified C3 are able to enter the nucleus of viable B cells, suggesting its potential involvement in regulation of gene transcription. ELISA, gel shift assay, confocal microscopy, and chromatin immunoprecipitation proved that C3 and C3a strongly bind to nuclear DNA, and among the interacting genes there are key factors of lymphocyte development and differentiation. The strong interaction of C3 with histone proteins and its potential ability to induce chromatin rearrangement suggest that C3/C3a might regulate DNA transcription via chromatin remodeling. Our data reveal a novel, hitherto undescribed role of C3 in immune cell homeostasis, which further extends the repertoire how complement links innate and adaptive immunity and regulates basic processes of the cells.https://www.frontiersin.org/article/10.3389/fimmu.2019.00493/fullcomplement C3internalizationDNAhistonesgene transcription
collection DOAJ
language English
format Article
sources DOAJ
author Mariann Kremlitzka
Alicja A. Nowacka
Frida C. Mohlin
Pradeep Bompada
Yang De Marinis
Anna M. Blom
spellingShingle Mariann Kremlitzka
Alicja A. Nowacka
Frida C. Mohlin
Pradeep Bompada
Yang De Marinis
Anna M. Blom
Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription
Frontiers in Immunology
complement C3
internalization
DNA
histones
gene transcription
author_facet Mariann Kremlitzka
Alicja A. Nowacka
Frida C. Mohlin
Pradeep Bompada
Yang De Marinis
Anna M. Blom
author_sort Mariann Kremlitzka
title Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription
title_short Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription
title_full Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription
title_fullStr Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription
title_full_unstemmed Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells—A Potential Involvement in Regulation of Gene Transcription
title_sort interaction of serum-derived and internalized c3 with dna in human b cells—a potential involvement in regulation of gene transcription
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-03-01
description Beside its classical role as a serum effector system of innate immunity, evidence is accumulating that complement has an intracellular repertoire of components that provides not only immune defense, but also functions to maintain cellular homeostasis. While complement proteins, mainly the central component C3, have been detected in B cells, their exact function and source remain largely unexplored. In this study, we investigated the expression and origin of intracellular C3 in human B cells together with its role in B cell homeostasis. Our data provide evidence that endogenous expression of C3 is very low in human B cells and, in accordance with the recent publication, the main origin of intracellular C3 is the serum. Interestingly, we found that both serum-derived and purified C3 are able to enter the nucleus of viable B cells, suggesting its potential involvement in regulation of gene transcription. ELISA, gel shift assay, confocal microscopy, and chromatin immunoprecipitation proved that C3 and C3a strongly bind to nuclear DNA, and among the interacting genes there are key factors of lymphocyte development and differentiation. The strong interaction of C3 with histone proteins and its potential ability to induce chromatin rearrangement suggest that C3/C3a might regulate DNA transcription via chromatin remodeling. Our data reveal a novel, hitherto undescribed role of C3 in immune cell homeostasis, which further extends the repertoire how complement links innate and adaptive immunity and regulates basic processes of the cells.
topic complement C3
internalization
DNA
histones
gene transcription
url https://www.frontiersin.org/article/10.3389/fimmu.2019.00493/full
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