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Mitochondria Activity and CXCR4 Collaboratively Promote the Differentiation of CD11c+ B Cells Induced by TLR9 in Lupus
Lupus is characterized by the autoantibodies against nuclear Ags, underscoring the importance of identifying the B cell subsets driving autoimmunity. Our research focused on the mitochondrial activity and CXCR4 expression in CD11c B cells from lupus patients after stimulation with a TLR9 agonist, Cp...
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Published in: | Immune network 2024-08, Vol.24 (4), p.9-22 |
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container_title | Immune network |
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creator | Jang, Sung Hoon Shim, Joo Sung Kim, Jieun Shin, Eun Gyeol Yoon, Jong Hwi Lee, Lucy Eunju Kwon, Ho-Keun Song, Jason Jungsik |
description | Lupus is characterized by the autoantibodies against nuclear Ags, underscoring the importance of identifying the B cell subsets driving autoimmunity. Our research focused on the mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients after
stimulation with a TLR9 agonist, CpG-oligodeoxyribonucleotide (ODN). We also evaluated the response of CD11c
B cells in ODN-injected mice. Post-
ODN stimulation, we observed an increase in the proportion of CD11c
cells, with elevated mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients.
experiments showed similar patterns, with TLR9 stimulation enhancing mitochondrial and CXCR4 activities in CD11c
B cells, leading to the generation of anti-dsDNA plasmablasts. The CXCR4 inhibitor AMD3100 and the mitochondrial complex I inhibitor IM156 significantly reduced the proportion of CD11c
B cells and autoreactive plasmablasts. These results underscore the pivotal roles of mitochondria and CXCR4 in the production of autoreactive plasmablasts. |
doi_str_mv | 10.4110/in.2024.24.e25 |
format | article |
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B cells from lupus patients after
stimulation with a TLR9 agonist, CpG-oligodeoxyribonucleotide (ODN). We also evaluated the response of CD11c
B cells in ODN-injected mice. Post-
ODN stimulation, we observed an increase in the proportion of CD11c
cells, with elevated mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients.
experiments showed similar patterns, with TLR9 stimulation enhancing mitochondrial and CXCR4 activities in CD11c
B cells, leading to the generation of anti-dsDNA plasmablasts. The CXCR4 inhibitor AMD3100 and the mitochondrial complex I inhibitor IM156 significantly reduced the proportion of CD11c
B cells and autoreactive plasmablasts. These results underscore the pivotal roles of mitochondria and CXCR4 in the production of autoreactive plasmablasts.</description><identifier>ISSN: 1598-2629</identifier><identifier>EISSN: 2092-6685</identifier><identifier>DOI: 10.4110/in.2024.24.e25</identifier><identifier>PMID: 39246618</identifier><language>eng</language><publisher>Korea (South): 대한면역학회</publisher><ispartof>Immune network, 2024-08, Vol.24 (4), p.9-22</ispartof><rights>Copyright © 2024. The Korean Association of Immunologists.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c250t-e332f26b2125fc4b0c5ccab47f317e3a0b89a8469391a719ca409b0686dbbaee3</cites><orcidid>0000-0002-3756-0189 ; 0000-0003-3175-0376 ; 0000-0003-0662-7704</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39246618$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jang, Sung Hoon</creatorcontrib><creatorcontrib>Shim, Joo Sung</creatorcontrib><creatorcontrib>Kim, Jieun</creatorcontrib><creatorcontrib>Shin, Eun Gyeol</creatorcontrib><creatorcontrib>Yoon, Jong Hwi</creatorcontrib><creatorcontrib>Lee, Lucy Eunju</creatorcontrib><creatorcontrib>Kwon, Ho-Keun</creatorcontrib><creatorcontrib>Song, Jason Jungsik</creatorcontrib><title>Mitochondria Activity and CXCR4 Collaboratively Promote the Differentiation of CD11c+ B Cells Induced by TLR9 in Lupus</title><title>Immune network</title><addtitle>Immune Netw</addtitle><description>Lupus is characterized by the autoantibodies against nuclear Ags, underscoring the importance of identifying the B cell subsets driving autoimmunity. Our research focused on the mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients after
stimulation with a TLR9 agonist, CpG-oligodeoxyribonucleotide (ODN). We also evaluated the response of CD11c
B cells in ODN-injected mice. Post-
ODN stimulation, we observed an increase in the proportion of CD11c
cells, with elevated mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients.
experiments showed similar patterns, with TLR9 stimulation enhancing mitochondrial and CXCR4 activities in CD11c
B cells, leading to the generation of anti-dsDNA plasmablasts. The CXCR4 inhibitor AMD3100 and the mitochondrial complex I inhibitor IM156 significantly reduced the proportion of CD11c
B cells and autoreactive plasmablasts. These results underscore the pivotal roles of mitochondria and CXCR4 in the production of autoreactive plasmablasts.</description><issn>1598-2629</issn><issn>2092-6685</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kE1rGzEQhkVpaRy31x6LLoVAWEdfq10dk7WTBtykBBd6WyTtLFFZS460a_C_j4LdwMAc3mdehgehb5QsBKXkyvkFI0ws8gArP6AZI4oVUtblRzSjpaoLJpk6Q-cp_SNECl6Vn9EZV0xISesZ2v9yY7DPwXfRaXxtR7d34wFr3-Hmb_MkcBOGQZsQdU5gOODfMWzDCHh8Brx0fQ8R_OhyGjwOPW6WlNpLfIMbGIaE7303WeiwOeDN-klh5_F62k3pC_rU6yHB19Oeoz-3q03zs1g_3t031-vCspKMBXDOeiYNo6zsrTDEltZqI6qe0wq4JqZWuhZScUV1RZXVgihDZC07YzQAn6OLY-8uhpcJ0thuXbL5Ne0hTKnllDBSMS54RhdH1MaQUoS-3UW31fHQUtK-uW6db99ct3my63zw_dQ9mS107_h_uRn4cQT8lCPonH5nHh6XK0pVqSQj_BV2uIXc</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Jang, Sung Hoon</creator><creator>Shim, Joo Sung</creator><creator>Kim, Jieun</creator><creator>Shin, Eun Gyeol</creator><creator>Yoon, Jong Hwi</creator><creator>Lee, Lucy Eunju</creator><creator>Kwon, Ho-Keun</creator><creator>Song, Jason Jungsik</creator><general>대한면역학회</general><scope>DBRKI</scope><scope>TDB</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3756-0189</orcidid><orcidid>https://orcid.org/0000-0003-3175-0376</orcidid><orcidid>https://orcid.org/0000-0003-0662-7704</orcidid></search><sort><creationdate>20240801</creationdate><title>Mitochondria Activity and CXCR4 Collaboratively Promote the Differentiation of CD11c+ B Cells Induced by TLR9 in Lupus</title><author>Jang, Sung Hoon ; Shim, Joo Sung ; Kim, Jieun ; Shin, Eun Gyeol ; Yoon, Jong Hwi ; Lee, Lucy Eunju ; Kwon, Ho-Keun ; Song, Jason Jungsik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c250t-e332f26b2125fc4b0c5ccab47f317e3a0b89a8469391a719ca409b0686dbbaee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jang, Sung Hoon</creatorcontrib><creatorcontrib>Shim, Joo Sung</creatorcontrib><creatorcontrib>Kim, Jieun</creatorcontrib><creatorcontrib>Shin, Eun Gyeol</creatorcontrib><creatorcontrib>Yoon, Jong Hwi</creatorcontrib><creatorcontrib>Lee, Lucy Eunju</creatorcontrib><creatorcontrib>Kwon, Ho-Keun</creatorcontrib><creatorcontrib>Song, Jason Jungsik</creatorcontrib><collection>DBPIA - 디비피아</collection><collection>DBPIA</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Immune network</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jang, Sung Hoon</au><au>Shim, Joo Sung</au><au>Kim, Jieun</au><au>Shin, Eun Gyeol</au><au>Yoon, Jong Hwi</au><au>Lee, Lucy Eunju</au><au>Kwon, Ho-Keun</au><au>Song, Jason Jungsik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondria Activity and CXCR4 Collaboratively Promote the Differentiation of CD11c+ B Cells Induced by TLR9 in Lupus</atitle><jtitle>Immune network</jtitle><addtitle>Immune Netw</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>24</volume><issue>4</issue><spage>9</spage><epage>22</epage><pages>9-22</pages><issn>1598-2629</issn><eissn>2092-6685</eissn><abstract>Lupus is characterized by the autoantibodies against nuclear Ags, underscoring the importance of identifying the B cell subsets driving autoimmunity. Our research focused on the mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients after
stimulation with a TLR9 agonist, CpG-oligodeoxyribonucleotide (ODN). We also evaluated the response of CD11c
B cells in ODN-injected mice. Post-
ODN stimulation, we observed an increase in the proportion of CD11c
cells, with elevated mitochondrial activity and CXCR4 expression in CD11c
B cells from lupus patients.
experiments showed similar patterns, with TLR9 stimulation enhancing mitochondrial and CXCR4 activities in CD11c
B cells, leading to the generation of anti-dsDNA plasmablasts. The CXCR4 inhibitor AMD3100 and the mitochondrial complex I inhibitor IM156 significantly reduced the proportion of CD11c
B cells and autoreactive plasmablasts. These results underscore the pivotal roles of mitochondria and CXCR4 in the production of autoreactive plasmablasts.</abstract><cop>Korea (South)</cop><pub>대한면역학회</pub><pmid>39246618</pmid><doi>10.4110/in.2024.24.e25</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-3756-0189</orcidid><orcidid>https://orcid.org/0000-0003-3175-0376</orcidid><orcidid>https://orcid.org/0000-0003-0662-7704</orcidid><oa>free_for_read</oa></addata></record> |
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title | Mitochondria Activity and CXCR4 Collaboratively Promote the Differentiation of CD11c+ B Cells Induced by TLR9 in Lupus |
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