PRDM1 expression via human parvovirus B19 infection plays a role in the pathogenesis of Hashimoto thyroiditis

Summary Ectopic lymphoid follicle infiltration is a key event in Hashimoto thyroiditis (HT). Positive regulatory domain zinc finger protein 1 (PRDM1), which is induced by antigen stimulation, can regulate all lymphocyte lineages. Several groups independently demonstrated that human parvovirus B19 (P...

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Veröffentlicht in:Human pathology 2015-12, Vol.46 (12), p.1913-1921
Hauptverfasser: Wang, Lu, MD, Zhang, Wei-Ping, MD, Yao, Li, MSc, Zhang, Wei, MD, Zhu, Jin, MD, Zhang, Wei-Chen, MSc, Zhang, Yue-Hua, MSc, Wang, Zhe, MD, Yan, Qing-Guo, MD, Guo, Ying, MD, Fan, Lin-Ni, MD, Liu, Yi-Xiong, MSc, Huang, Gao-Sheng, MD
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container_end_page 1921
container_issue 12
container_start_page 1913
container_title Human pathology
container_volume 46
creator Wang, Lu, MD
Zhang, Wei-Ping, MD
Yao, Li, MSc
Zhang, Wei, MD
Zhu, Jin, MD
Zhang, Wei-Chen, MSc
Zhang, Yue-Hua, MSc
Wang, Zhe, MD
Yan, Qing-Guo, MD
Guo, Ying, MD
Fan, Lin-Ni, MD
Liu, Yi-Xiong, MSc
Huang, Gao-Sheng, MD
description Summary Ectopic lymphoid follicle infiltration is a key event in Hashimoto thyroiditis (HT). Positive regulatory domain zinc finger protein 1 (PRDM1), which is induced by antigen stimulation, can regulate all lymphocyte lineages. Several groups independently demonstrated that human parvovirus B19 (PVB19) is closely associated with HT. Hence, we determined whether PRDM1 is expressed in HT thyroid tissue and whether there is any correlation between PRDM1 expression and PVB19 in the pathogenesis of HT. We detected PRDM1 expression in HT (n = 86), normal thyroid tissue (n = 30), and nontoxic nodular goiter (n = 20) samples using immunohistochemistry. We also detected PVB19 protein in HT samples in a double-blind manner and analyzed the correlation between the 2 proteins using immunofluorescence confocal detection and coimmunoprecipitation. Furthermore, we detected changes of the expression levels of PRDM1 and PVB19 in transfected primary thyroid follicular epithelial cells using real-time quantitative polymerase chain reaction. We found that PRDM1 protein is significantly highly expressed in the injured follicular epithelial cells in HT (83/86 cases) than in normal thyroid cells (0/30 cases) or in nontoxic nodular goiter cells (0/20 cases) ( P < .001). In HT, the PRDM1 expression pattern was the same as that of PVB19, whereas PRDM1 and PVB19 were coexistent in the involved epithelial cells. Statistical analysis showed a significant correlation between PRDM1 and PVB19 ( P < .001). In addition, primary thyroid epithelial cells also showed PRDM1 up-regulation after PVB19 NS1 transfection. Our findings suggest a previously unrecognized role of PRDM1 and PVB19 in the pathogenesis of HT.
doi_str_mv 10.1016/j.humpath.2015.08.009
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Positive regulatory domain zinc finger protein 1 (PRDM1), which is induced by antigen stimulation, can regulate all lymphocyte lineages. Several groups independently demonstrated that human parvovirus B19 (PVB19) is closely associated with HT. Hence, we determined whether PRDM1 is expressed in HT thyroid tissue and whether there is any correlation between PRDM1 expression and PVB19 in the pathogenesis of HT. We detected PRDM1 expression in HT (n = 86), normal thyroid tissue (n = 30), and nontoxic nodular goiter (n = 20) samples using immunohistochemistry. We also detected PVB19 protein in HT samples in a double-blind manner and analyzed the correlation between the 2 proteins using immunofluorescence confocal detection and coimmunoprecipitation. Furthermore, we detected changes of the expression levels of PRDM1 and PVB19 in transfected primary thyroid follicular epithelial cells using real-time quantitative polymerase chain reaction. We found that PRDM1 protein is significantly highly expressed in the injured follicular epithelial cells in HT (83/86 cases) than in normal thyroid cells (0/30 cases) or in nontoxic nodular goiter cells (0/20 cases) ( P &lt; .001). In HT, the PRDM1 expression pattern was the same as that of PVB19, whereas PRDM1 and PVB19 were coexistent in the involved epithelial cells. Statistical analysis showed a significant correlation between PRDM1 and PVB19 ( P &lt; .001). In addition, primary thyroid epithelial cells also showed PRDM1 up-regulation after PVB19 NS1 transfection. Our findings suggest a previously unrecognized role of PRDM1 and PVB19 in the pathogenesis of HT.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2015.08.009</identifier><identifier>PMID: 26475096</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Antigens ; Binding sites ; Cloning ; Deoxyribonucleic acid ; DNA ; Ectopic lymphoid tissue ; Female ; Fluorescent Antibody Technique ; Gene expression ; Hashimoto Disease - immunology ; Hashimoto Disease - pathology ; Hashimoto Disease - virology ; Hashimoto's thyroiditis ; Hospitals ; Human parvovirus B19 ; Humans ; Immunohistochemistry ; Immunoprecipitation ; Infections ; Methods ; Microscopy, Confocal ; Middle Aged ; Parvoviridae Infections - immunology ; Parvoviridae Infections - metabolism ; Parvovirus B19, Human ; Pathogenesis ; Pathology ; Polymerase chain reaction ; Positive Regulatory Domain I-Binding Factor 1 ; Positive regulatory domain zinc finger protein 1 ; Proteins ; Real-Time Polymerase Chain Reaction ; Repressor Proteins - biosynthesis ; Retrospective Studies ; Tissue Array Analysis ; Viral infections ; Young Adult</subject><ispartof>Human pathology, 2015-12, Vol.46 (12), p.1913-1921</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Dec 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-36d7efdcedb055a9e29fccb3558a79a3270cd3a64b90608403f67995b29e90e33</citedby><cites>FETCH-LOGICAL-c448t-36d7efdcedb055a9e29fccb3558a79a3270cd3a64b90608403f67995b29e90e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.humpath.2015.08.009$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26475096$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Lu, MD</creatorcontrib><creatorcontrib>Zhang, Wei-Ping, MD</creatorcontrib><creatorcontrib>Yao, Li, MSc</creatorcontrib><creatorcontrib>Zhang, Wei, MD</creatorcontrib><creatorcontrib>Zhu, Jin, MD</creatorcontrib><creatorcontrib>Zhang, Wei-Chen, MSc</creatorcontrib><creatorcontrib>Zhang, Yue-Hua, MSc</creatorcontrib><creatorcontrib>Wang, Zhe, MD</creatorcontrib><creatorcontrib>Yan, Qing-Guo, MD</creatorcontrib><creatorcontrib>Guo, Ying, MD</creatorcontrib><creatorcontrib>Fan, Lin-Ni, MD</creatorcontrib><creatorcontrib>Liu, Yi-Xiong, MSc</creatorcontrib><creatorcontrib>Huang, Gao-Sheng, MD</creatorcontrib><title>PRDM1 expression via human parvovirus B19 infection plays a role in the pathogenesis of Hashimoto thyroiditis</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Summary Ectopic lymphoid follicle infiltration is a key event in Hashimoto thyroiditis (HT). Positive regulatory domain zinc finger protein 1 (PRDM1), which is induced by antigen stimulation, can regulate all lymphocyte lineages. Several groups independently demonstrated that human parvovirus B19 (PVB19) is closely associated with HT. Hence, we determined whether PRDM1 is expressed in HT thyroid tissue and whether there is any correlation between PRDM1 expression and PVB19 in the pathogenesis of HT. We detected PRDM1 expression in HT (n = 86), normal thyroid tissue (n = 30), and nontoxic nodular goiter (n = 20) samples using immunohistochemistry. We also detected PVB19 protein in HT samples in a double-blind manner and analyzed the correlation between the 2 proteins using immunofluorescence confocal detection and coimmunoprecipitation. Furthermore, we detected changes of the expression levels of PRDM1 and PVB19 in transfected primary thyroid follicular epithelial cells using real-time quantitative polymerase chain reaction. We found that PRDM1 protein is significantly highly expressed in the injured follicular epithelial cells in HT (83/86 cases) than in normal thyroid cells (0/30 cases) or in nontoxic nodular goiter cells (0/20 cases) ( P &lt; .001). In HT, the PRDM1 expression pattern was the same as that of PVB19, whereas PRDM1 and PVB19 were coexistent in the involved epithelial cells. Statistical analysis showed a significant correlation between PRDM1 and PVB19 ( P &lt; .001). In addition, primary thyroid epithelial cells also showed PRDM1 up-regulation after PVB19 NS1 transfection. 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Zhang, Wei-Ping, MD ; Yao, Li, MSc ; Zhang, Wei, MD ; Zhu, Jin, MD ; Zhang, Wei-Chen, MSc ; Zhang, Yue-Hua, MSc ; Wang, Zhe, MD ; Yan, Qing-Guo, MD ; Guo, Ying, MD ; Fan, Lin-Ni, MD ; Liu, Yi-Xiong, MSc ; Huang, Gao-Sheng, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-36d7efdcedb055a9e29fccb3558a79a3270cd3a64b90608403f67995b29e90e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antigens</topic><topic>Binding sites</topic><topic>Cloning</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Ectopic lymphoid tissue</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Gene expression</topic><topic>Hashimoto Disease - immunology</topic><topic>Hashimoto Disease - pathology</topic><topic>Hashimoto Disease - virology</topic><topic>Hashimoto's thyroiditis</topic><topic>Hospitals</topic><topic>Human parvovirus B19</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunoprecipitation</topic><topic>Infections</topic><topic>Methods</topic><topic>Microscopy, Confocal</topic><topic>Middle Aged</topic><topic>Parvoviridae Infections - immunology</topic><topic>Parvoviridae Infections - metabolism</topic><topic>Parvovirus B19, Human</topic><topic>Pathogenesis</topic><topic>Pathology</topic><topic>Polymerase chain reaction</topic><topic>Positive Regulatory Domain I-Binding Factor 1</topic><topic>Positive regulatory domain zinc finger protein 1</topic><topic>Proteins</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Repressor Proteins - biosynthesis</topic><topic>Retrospective Studies</topic><topic>Tissue Array Analysis</topic><topic>Viral infections</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Lu, MD</creatorcontrib><creatorcontrib>Zhang, Wei-Ping, MD</creatorcontrib><creatorcontrib>Yao, Li, MSc</creatorcontrib><creatorcontrib>Zhang, Wei, MD</creatorcontrib><creatorcontrib>Zhu, Jin, MD</creatorcontrib><creatorcontrib>Zhang, Wei-Chen, MSc</creatorcontrib><creatorcontrib>Zhang, Yue-Hua, MSc</creatorcontrib><creatorcontrib>Wang, Zhe, MD</creatorcontrib><creatorcontrib>Yan, Qing-Guo, MD</creatorcontrib><creatorcontrib>Guo, Ying, MD</creatorcontrib><creatorcontrib>Fan, Lin-Ni, MD</creatorcontrib><creatorcontrib>Liu, Yi-Xiong, MSc</creatorcontrib><creatorcontrib>Huang, Gao-Sheng, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Lu, MD</au><au>Zhang, Wei-Ping, MD</au><au>Yao, Li, MSc</au><au>Zhang, Wei, MD</au><au>Zhu, Jin, MD</au><au>Zhang, Wei-Chen, MSc</au><au>Zhang, Yue-Hua, MSc</au><au>Wang, Zhe, MD</au><au>Yan, Qing-Guo, MD</au><au>Guo, Ying, MD</au><au>Fan, Lin-Ni, MD</au><au>Liu, Yi-Xiong, MSc</au><au>Huang, Gao-Sheng, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PRDM1 expression via human parvovirus B19 infection plays a role in the pathogenesis of Hashimoto thyroiditis</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>46</volume><issue>12</issue><spage>1913</spage><epage>1921</epage><pages>1913-1921</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Summary Ectopic lymphoid follicle infiltration is a key event in Hashimoto thyroiditis (HT). Positive regulatory domain zinc finger protein 1 (PRDM1), which is induced by antigen stimulation, can regulate all lymphocyte lineages. Several groups independently demonstrated that human parvovirus B19 (PVB19) is closely associated with HT. Hence, we determined whether PRDM1 is expressed in HT thyroid tissue and whether there is any correlation between PRDM1 expression and PVB19 in the pathogenesis of HT. We detected PRDM1 expression in HT (n = 86), normal thyroid tissue (n = 30), and nontoxic nodular goiter (n = 20) samples using immunohistochemistry. We also detected PVB19 protein in HT samples in a double-blind manner and analyzed the correlation between the 2 proteins using immunofluorescence confocal detection and coimmunoprecipitation. Furthermore, we detected changes of the expression levels of PRDM1 and PVB19 in transfected primary thyroid follicular epithelial cells using real-time quantitative polymerase chain reaction. We found that PRDM1 protein is significantly highly expressed in the injured follicular epithelial cells in HT (83/86 cases) than in normal thyroid cells (0/30 cases) or in nontoxic nodular goiter cells (0/20 cases) ( P &lt; .001). In HT, the PRDM1 expression pattern was the same as that of PVB19, whereas PRDM1 and PVB19 were coexistent in the involved epithelial cells. Statistical analysis showed a significant correlation between PRDM1 and PVB19 ( P &lt; .001). In addition, primary thyroid epithelial cells also showed PRDM1 up-regulation after PVB19 NS1 transfection. Our findings suggest a previously unrecognized role of PRDM1 and PVB19 in the pathogenesis of HT.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26475096</pmid><doi>10.1016/j.humpath.2015.08.009</doi><tpages>9</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Antigens
Binding sites
Cloning
Deoxyribonucleic acid
DNA
Ectopic lymphoid tissue
Female
Fluorescent Antibody Technique
Gene expression
Hashimoto Disease - immunology
Hashimoto Disease - pathology
Hashimoto Disease - virology
Hashimoto's thyroiditis
Hospitals
Human parvovirus B19
Humans
Immunohistochemistry
Immunoprecipitation
Infections
Methods
Microscopy, Confocal
Middle Aged
Parvoviridae Infections - immunology
Parvoviridae Infections - metabolism
Parvovirus B19, Human
Pathogenesis
Pathology
Polymerase chain reaction
Positive Regulatory Domain I-Binding Factor 1
Positive regulatory domain zinc finger protein 1
Proteins
Real-Time Polymerase Chain Reaction
Repressor Proteins - biosynthesis
Retrospective Studies
Tissue Array Analysis
Viral infections
Young Adult
title PRDM1 expression via human parvovirus B19 infection plays a role in the pathogenesis of Hashimoto thyroiditis
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