Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas

Follicular dendritic cells (FDC) show homo- and heterocellular metabolic coupling through connexin 43 (Cx43) gap junctions and support B cell selection and maturation in germinal centers. In follicular lymphomas B cells escape apoptosis while FDC develop abnormally. Here we tested Cx43 channels in r...

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Main Authors: Hajnalka Rajnai, Ivett Teleki, Gergo Kiszner, Nora Meggyesházi, Peter Balla, Tamas Vancsik, Gyorgyi Muzes, Judit Csomor, Andras Matolcsy, Tibor Krenacs
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2015/528098
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author Hajnalka Rajnai
Ivett Teleki
Gergo Kiszner
Nora Meggyesházi
Peter Balla
Tamas Vancsik
Gyorgyi Muzes
Judit Csomor
Andras Matolcsy
Tibor Krenacs
author_facet Hajnalka Rajnai
Ivett Teleki
Gergo Kiszner
Nora Meggyesházi
Peter Balla
Tamas Vancsik
Gyorgyi Muzes
Judit Csomor
Andras Matolcsy
Tibor Krenacs
author_sort Hajnalka Rajnai
collection DOAJ
description Follicular dendritic cells (FDC) show homo- and heterocellular metabolic coupling through connexin 43 (Cx43) gap junctions and support B cell selection and maturation in germinal centers. In follicular lymphomas B cells escape apoptosis while FDC develop abnormally. Here we tested Cx43 channels in reactive FDC development and follicular lymphomas. In culture, the treatment of FDC-B cell clusters (resembling to “ex vivo” germinal centers) with Gap27 peptide, mimicking the 2nd extracellular loop of Cx43 protein, significantly impaired FDC-B cell cluster formation and cell survival. In untreated cultures of intact clusters, cell proliferation showed a moderate reduction. In tissues, Cx43 protein levels run parallel with the density of FDC both in reactive germinal centers and in malformed follicles of follicular lymphomas and showed strong upregulation in newly generated and/or degrading bi-/multinuclear FDC of rudimentary processes. However, the inverse correlation between Cx43 expression and B cell proliferation seen in reactive germinal centers was not detected in follicular lymphomas. Furthermore, Cx43 levels were not associated with either lymphoma grade or bone marrow involvement. Our results suggest that Cx43 channels are critical in FDC and “ex vivo” germinal center development and in the persistence of FDC in follicular lymphomas but do not affect tumor progression.
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spelling doaj-art-9775284888564a0aa1d0f2461de065b22025-02-03T01:01:51ZengWileyJournal of Immunology Research2314-88612314-71562015-01-01201510.1155/2015/528098528098Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular LymphomasHajnalka Rajnai0Ivett Teleki1Gergo Kiszner2Nora Meggyesházi3Peter Balla4Tamas Vancsik5Gyorgyi Muzes6Judit Csomor7Andras Matolcsy8Tibor Krenacs91st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary2nd Department of Internal Medicine, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, Hungary1st Department of Pathology and Experimental Cancer Research, 1085 Budapest, HungaryFollicular dendritic cells (FDC) show homo- and heterocellular metabolic coupling through connexin 43 (Cx43) gap junctions and support B cell selection and maturation in germinal centers. In follicular lymphomas B cells escape apoptosis while FDC develop abnormally. Here we tested Cx43 channels in reactive FDC development and follicular lymphomas. In culture, the treatment of FDC-B cell clusters (resembling to “ex vivo” germinal centers) with Gap27 peptide, mimicking the 2nd extracellular loop of Cx43 protein, significantly impaired FDC-B cell cluster formation and cell survival. In untreated cultures of intact clusters, cell proliferation showed a moderate reduction. In tissues, Cx43 protein levels run parallel with the density of FDC both in reactive germinal centers and in malformed follicles of follicular lymphomas and showed strong upregulation in newly generated and/or degrading bi-/multinuclear FDC of rudimentary processes. However, the inverse correlation between Cx43 expression and B cell proliferation seen in reactive germinal centers was not detected in follicular lymphomas. Furthermore, Cx43 levels were not associated with either lymphoma grade or bone marrow involvement. Our results suggest that Cx43 channels are critical in FDC and “ex vivo” germinal center development and in the persistence of FDC in follicular lymphomas but do not affect tumor progression.http://dx.doi.org/10.1155/2015/528098
spellingShingle Hajnalka Rajnai
Ivett Teleki
Gergo Kiszner
Nora Meggyesházi
Peter Balla
Tamas Vancsik
Gyorgyi Muzes
Judit Csomor
Andras Matolcsy
Tibor Krenacs
Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas
Journal of Immunology Research
title Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas
title_full Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas
title_fullStr Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas
title_full_unstemmed Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas
title_short Connexin 43 Communication Channels in Follicular Dendritic Cell Development and in Follicular Lymphomas
title_sort connexin 43 communication channels in follicular dendritic cell development and in follicular lymphomas
url http://dx.doi.org/10.1155/2015/528098
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