B-cell lymphoma 6 promotes proliferation and survival of trophoblastic cells
Preeclampsia is one of the leading causes of maternal and perinatal mortality and morbidity and its pathogenesis is not fully understood. B-cell lymphoma 6 (BCL6), a key regulator of B-lymphocyte development, is altered in preeclamptic placentas. We show here that BCL6 is present in all 3 studied tr...
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creator | Muschol-Steinmetz, Cornelia Jasmer, Britta Nina-Naomi Kreis Steinhäuser, Kerstin Ritter, Andreas Rolle, Udo Juping Yuan Louwen, Frank |
description | Preeclampsia is one of the leading causes of maternal and perinatal mortality and morbidity and its pathogenesis is not fully understood. B-cell lymphoma 6 (BCL6), a key regulator of B-lymphocyte development, is altered in preeclamptic placentas. We show here that BCL6 is present in all 3 studied trophoblast cell lines and it is predominantly expressed in trophoblastic HTR-8/SVneo cells derived from a 1st trimester placenta, suggestive of its involvement in trophoblast expansion in the early stage of placental development. BCL6 is strongly stabilized upon stress stimulation. Inhibition of BCL6, by administrating either small interfering RNA or a specific small molecule inhibitor 79–6, reduces proliferation and induces apoptosis in trophoblastic cells. Intriguingly, depletion of BCL6 in HTR-8/SVneo cells results in a mitotic arrest associated with mitotic defects in centrosome integrity, indicative of its involvement in mitotic progression. Thus, like in haematopoietic cells and breast cancer cells, BCL6 promotes proliferation and facilitates survival of trophoblasts under stress situation. Further studies are required to decipher its molecular roles in differentiation, migration and the fusion process of trophoblasts. Whether increased BCL6 observed in preeclamptic placentas is one of the causes or the consequences of preeclampsia warrants further investigations in vivo and in vitro. |
doi_str_mv | 10.6084/m9.figshare.3142297 |
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B-cell lymphoma 6 (BCL6), a key regulator of B-lymphocyte development, is altered in preeclamptic placentas. We show here that BCL6 is present in all 3 studied trophoblast cell lines and it is predominantly expressed in trophoblastic HTR-8/SVneo cells derived from a 1st trimester placenta, suggestive of its involvement in trophoblast expansion in the early stage of placental development. BCL6 is strongly stabilized upon stress stimulation. Inhibition of BCL6, by administrating either small interfering RNA or a specific small molecule inhibitor 79–6, reduces proliferation and induces apoptosis in trophoblastic cells. Intriguingly, depletion of BCL6 in HTR-8/SVneo cells results in a mitotic arrest associated with mitotic defects in centrosome integrity, indicative of its involvement in mitotic progression. Thus, like in haematopoietic cells and breast cancer cells, BCL6 promotes proliferation and facilitates survival of trophoblasts under stress situation. Further studies are required to decipher its molecular roles in differentiation, migration and the fusion process of trophoblasts. Whether increased BCL6 observed in preeclamptic placentas is one of the causes or the consequences of preeclampsia warrants further investigations in vivo and in vitro.</description><identifier>DOI: 10.6084/m9.figshare.3142297</identifier><language>eng</language><publisher>Taylor & Francis</publisher><subject>Biological Sciences not elsewhere classified ; Cancer ; Cell Biology ; Developmental Biology ; FOS: Biological sciences ; FOS: Clinical medicine ; FOS: Health sciences ; Hematology ; Immunology ; Infectious Diseases</subject><creationdate>2016</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1887</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.3142297$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Muschol-Steinmetz, Cornelia</creatorcontrib><creatorcontrib>Jasmer, Britta</creatorcontrib><creatorcontrib>Nina-Naomi Kreis</creatorcontrib><creatorcontrib>Steinhäuser, Kerstin</creatorcontrib><creatorcontrib>Ritter, Andreas</creatorcontrib><creatorcontrib>Rolle, Udo</creatorcontrib><creatorcontrib>Juping Yuan</creatorcontrib><creatorcontrib>Louwen, Frank</creatorcontrib><title>B-cell lymphoma 6 promotes proliferation and survival of trophoblastic cells</title><description>Preeclampsia is one of the leading causes of maternal and perinatal mortality and morbidity and its pathogenesis is not fully understood. B-cell lymphoma 6 (BCL6), a key regulator of B-lymphocyte development, is altered in preeclamptic placentas. We show here that BCL6 is present in all 3 studied trophoblast cell lines and it is predominantly expressed in trophoblastic HTR-8/SVneo cells derived from a 1st trimester placenta, suggestive of its involvement in trophoblast expansion in the early stage of placental development. BCL6 is strongly stabilized upon stress stimulation. Inhibition of BCL6, by administrating either small interfering RNA or a specific small molecule inhibitor 79–6, reduces proliferation and induces apoptosis in trophoblastic cells. Intriguingly, depletion of BCL6 in HTR-8/SVneo cells results in a mitotic arrest associated with mitotic defects in centrosome integrity, indicative of its involvement in mitotic progression. Thus, like in haematopoietic cells and breast cancer cells, BCL6 promotes proliferation and facilitates survival of trophoblasts under stress situation. Further studies are required to decipher its molecular roles in differentiation, migration and the fusion process of trophoblasts. Whether increased BCL6 observed in preeclamptic placentas is one of the causes or the consequences of preeclampsia warrants further investigations in vivo and in vitro.</description><subject>Biological Sciences not elsewhere classified</subject><subject>Cancer</subject><subject>Cell Biology</subject><subject>Developmental Biology</subject><subject>FOS: Biological sciences</subject><subject>FOS: Clinical medicine</subject><subject>FOS: Health sciences</subject><subject>Hematology</subject><subject>Immunology</subject><subject>Infectious Diseases</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2016</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNqdjr0OgjAURrs4GPUJXO4LgPwFZdVoHBzdmyu0cJNbStpKwtsrCb6A0_ct5-QIsU-TuExOxcFUsabWd-hUnKdFllXHtXico1oxA09m6KxBKGFw1tig_HyYtHIYyPaAfQP-7UYakcFqCM5-iRejD1TDLPFbsdLIXu2W3Yj8dn1e7lGDAWsKSg6ODLpJpomcm6Sp5K9JLk35f9QH7TNK7w</recordid><startdate>20160331</startdate><enddate>20160331</enddate><creator>Muschol-Steinmetz, Cornelia</creator><creator>Jasmer, Britta</creator><creator>Nina-Naomi Kreis</creator><creator>Steinhäuser, Kerstin</creator><creator>Ritter, Andreas</creator><creator>Rolle, Udo</creator><creator>Juping Yuan</creator><creator>Louwen, Frank</creator><general>Taylor & Francis</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20160331</creationdate><title>B-cell lymphoma 6 promotes proliferation and survival of trophoblastic cells</title><author>Muschol-Steinmetz, Cornelia ; Jasmer, Britta ; Nina-Naomi Kreis ; Steinhäuser, Kerstin ; Ritter, Andreas ; Rolle, Udo ; Juping Yuan ; Louwen, Frank</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_31422973</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biological Sciences not elsewhere classified</topic><topic>Cancer</topic><topic>Cell Biology</topic><topic>Developmental Biology</topic><topic>FOS: Biological sciences</topic><topic>FOS: Clinical medicine</topic><topic>FOS: Health sciences</topic><topic>Hematology</topic><topic>Immunology</topic><topic>Infectious Diseases</topic><toplevel>online_resources</toplevel><creatorcontrib>Muschol-Steinmetz, Cornelia</creatorcontrib><creatorcontrib>Jasmer, Britta</creatorcontrib><creatorcontrib>Nina-Naomi Kreis</creatorcontrib><creatorcontrib>Steinhäuser, Kerstin</creatorcontrib><creatorcontrib>Ritter, Andreas</creatorcontrib><creatorcontrib>Rolle, Udo</creatorcontrib><creatorcontrib>Juping Yuan</creatorcontrib><creatorcontrib>Louwen, Frank</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Muschol-Steinmetz, Cornelia</au><au>Jasmer, Britta</au><au>Nina-Naomi Kreis</au><au>Steinhäuser, Kerstin</au><au>Ritter, Andreas</au><au>Rolle, Udo</au><au>Juping Yuan</au><au>Louwen, Frank</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>B-cell lymphoma 6 promotes proliferation and survival of trophoblastic cells</title><date>2016-03-31</date><risdate>2016</risdate><abstract>Preeclampsia is one of the leading causes of maternal and perinatal mortality and morbidity and its pathogenesis is not fully understood. B-cell lymphoma 6 (BCL6), a key regulator of B-lymphocyte development, is altered in preeclamptic placentas. We show here that BCL6 is present in all 3 studied trophoblast cell lines and it is predominantly expressed in trophoblastic HTR-8/SVneo cells derived from a 1st trimester placenta, suggestive of its involvement in trophoblast expansion in the early stage of placental development. BCL6 is strongly stabilized upon stress stimulation. Inhibition of BCL6, by administrating either small interfering RNA or a specific small molecule inhibitor 79–6, reduces proliferation and induces apoptosis in trophoblastic cells. Intriguingly, depletion of BCL6 in HTR-8/SVneo cells results in a mitotic arrest associated with mitotic defects in centrosome integrity, indicative of its involvement in mitotic progression. Thus, like in haematopoietic cells and breast cancer cells, BCL6 promotes proliferation and facilitates survival of trophoblasts under stress situation. Further studies are required to decipher its molecular roles in differentiation, migration and the fusion process of trophoblasts. Whether increased BCL6 observed in preeclamptic placentas is one of the causes or the consequences of preeclampsia warrants further investigations in vivo and in vitro.</abstract><pub>Taylor & Francis</pub><doi>10.6084/m9.figshare.3142297</doi><oa>free_for_read</oa></addata></record> |
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subjects | Biological Sciences not elsewhere classified Cancer Cell Biology Developmental Biology FOS: Biological sciences FOS: Clinical medicine FOS: Health sciences Hematology Immunology Infectious Diseases |
title | B-cell lymphoma 6 promotes proliferation and survival of trophoblastic cells |
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