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Ginkgo biloba Induces Thrombomodulin Expression and Tissue-Type Plasminogen Activator Secretion via the Activation of Krüppel-Like Factor 2 within Endothelial Cells.

Identifieur interne : 000238 ( Main/Exploration ); précédent : 000237; suivant : 000239

Ginkgo biloba Induces Thrombomodulin Expression and Tissue-Type Plasminogen Activator Secretion via the Activation of Krüppel-Like Factor 2 within Endothelial Cells.

Auteurs : Yi-Lin Chiu [République populaire de Chine] ; Wei-Che Tsai [République populaire de Chine] ; Chih-Hsien Wu [République populaire de Chine] ; Chun-Hsien Wu [République populaire de Chine] ; Cheng-Chung Cheng [République populaire de Chine] ; Wei-Shing Lin [République populaire de Chine] ; Tsung-Neng Tsai [République populaire de Chine] ; Lian-Shan Wu [République populaire de Chine]

Source :

RBID : pubmed:32108493

Descripteurs français

English descriptors

Abstract

The effects of thrombo-prevention, such as antiplatelet and anticoagulant activity, have been reported with the usage of Ginkgo biloba extract (GbE); however, the detailed mechanism has not yet been fully investigated, especially the role of Krüppel-like factor 2 (KLF2). This study aimed to investigate whether GbE can activate KLF2 and then induce thrombomodulin (TM) and tissue-type plasminogen activator (t-PA) secretion to enhance the effects of thrombo-prevention. Different concentrations of GbE were incubated with human umbilical vein endothelial cells (HUVECs) to evaluate its effect on endothelial cells. We found that KLF2 expression is correlated to the risk of atherosclerosis and venous thromboembolism in clinical practice. In the HUVEC cell model, GbE stimulated the expression of KLF2 in a dose-dependent manner. Moreover, TM and t-PA secretion increased when the cells were cultured with GbE. Both the expressions and activities of TM and t-PA in the GbE-treated cells declined after KLF2 was blocked by shKLF2. In sum, with GbE treatment, KLF2 expression in human endothelial cells was significantly activated, which in turn induced an increase in the protein expression and activity of TM and t-PA. After shRNA inhibited the KLF2 expression, GbE stopped inducing the expression and activity of TM and t-PA. These findings suggest that GbE exerts an antithrombotic effect on endothelial cells by increasing the TM expression and t-PA secretion; further, KLF2 is a key factor in this mechanism.

DOI: 10.1142/S0192415X20500184
PubMed: 32108493


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<term>Kruppel-Like Transcription Factors (genetics)</term>
<term>Kruppel-Like Transcription Factors (metabolism)</term>
<term>Plant Extracts (pharmacology)</term>
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<term>Facteurs de transcription Krüppel-like</term>
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<div type="abstract" xml:lang="en">The effects of thrombo-prevention, such as antiplatelet and anticoagulant activity, have been reported with the usage of Ginkgo biloba extract (GbE); however, the detailed mechanism has not yet been fully investigated, especially the role of Krüppel-like factor 2 (KLF2). This study aimed to investigate whether GbE can activate KLF2 and then induce thrombomodulin (TM) and tissue-type plasminogen activator (t-PA) secretion to enhance the effects of thrombo-prevention. Different concentrations of GbE were incubated with human umbilical vein endothelial cells (HUVECs) to evaluate its effect on endothelial cells. We found that KLF2 expression is correlated to the risk of atherosclerosis and venous thromboembolism in clinical practice. In the HUVEC cell model, GbE stimulated the expression of KLF2 in a dose-dependent manner. Moreover, TM and t-PA secretion increased when the cells were cultured with GbE. Both the expressions and activities of TM and t-PA in the GbE-treated cells declined after KLF2 was blocked by shKLF2. In sum, with GbE treatment, KLF2 expression in human endothelial cells was significantly activated, which in turn induced an increase in the protein expression and activity of TM and t-PA. After shRNA inhibited the KLF2 expression, GbE stopped inducing the expression and activity of TM and t-PA. These findings suggest that GbE exerts an antithrombotic effect on endothelial cells by increasing the TM expression and t-PA secretion; further, KLF2 is a key factor in this mechanism.</div>
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Induces Thrombomodulin Expression and Tissue-Type Plasminogen Activator Secretion via the Activation of Krüppel-Like Factor 2 within Endothelial Cells.</ArticleTitle>
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<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D018180">Thrombomodulin</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>19FUJ2C58T</RegistryNumber>
<NameOfSubstance UI="C063170">Ginkgo biloba extract</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 3.4.21.68</RegistryNumber>
<NameOfSubstance UI="D010959">Tissue Plasminogen Activator</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D002478" MajorTopicYN="N">Cells, Cultured</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D042783" MajorTopicYN="N">Endothelial Cells</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015870" MajorTopicYN="N">Gene Expression</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D051741" MajorTopicYN="N">Kruppel-Like Transcription Factors</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010936" MajorTopicYN="N">Plant Extracts</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018180" MajorTopicYN="N">Thrombomodulin</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010959" MajorTopicYN="N">Tissue Plasminogen Activator</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Endothelial Cells</Keyword>
<Keyword MajorTopicYN="N">Ginkgo Biloba Extract</Keyword>
<Keyword MajorTopicYN="N">Krüppel-Like Factor 2</Keyword>
<Keyword MajorTopicYN="N">Thrombomodulin</Keyword>
<Keyword MajorTopicYN="N">Thrombosis</Keyword>
<Keyword MajorTopicYN="N">Tissue-Type Plasminogen Activator</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>2</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2020</Year>
<Month>8</Month>
<Day>28</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2020</Year>
<Month>2</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">32108493</ArticleId>
<ArticleId IdType="doi">10.1142/S0192415X20500184</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
</country>
</list>
<tree>
<country name="République populaire de Chine">
<noRegion>
<name sortKey="Chiu, Yi Lin" sort="Chiu, Yi Lin" uniqKey="Chiu Y" first="Yi-Lin" last="Chiu">Yi-Lin Chiu</name>
</noRegion>
<name sortKey="Cheng, Cheng Chung" sort="Cheng, Cheng Chung" uniqKey="Cheng C" first="Cheng-Chung" last="Cheng">Cheng-Chung Cheng</name>
<name sortKey="Lin, Wei Shing" sort="Lin, Wei Shing" uniqKey="Lin W" first="Wei-Shing" last="Lin">Wei-Shing Lin</name>
<name sortKey="Tsai, Tsung Neng" sort="Tsai, Tsung Neng" uniqKey="Tsai T" first="Tsung-Neng" last="Tsai">Tsung-Neng Tsai</name>
<name sortKey="Tsai, Tsung Neng" sort="Tsai, Tsung Neng" uniqKey="Tsai T" first="Tsung-Neng" last="Tsai">Tsung-Neng Tsai</name>
<name sortKey="Tsai, Wei Che" sort="Tsai, Wei Che" uniqKey="Tsai W" first="Wei-Che" last="Tsai">Wei-Che Tsai</name>
<name sortKey="Wu, Chih Hsien" sort="Wu, Chih Hsien" uniqKey="Wu C" first="Chih-Hsien" last="Wu">Chih-Hsien Wu</name>
<name sortKey="Wu, Chun Hsien" sort="Wu, Chun Hsien" uniqKey="Wu C" first="Chun-Hsien" last="Wu">Chun-Hsien Wu</name>
<name sortKey="Wu, Lian Shan" sort="Wu, Lian Shan" uniqKey="Wu L" first="Lian-Shan" last="Wu">Lian-Shan Wu</name>
</country>
</tree>
</affiliations>
</record>

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