Serveur d'exploration sur les récepteurs immunitaires végétaux

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Receptor and signaling pathway involved in bovine lymphocyte activation by Atractylodis macrocephalae polysaccharides.

Identifieur interne : 000072 ( Main/Exploration ); précédent : 000071; suivant : 000073

Receptor and signaling pathway involved in bovine lymphocyte activation by Atractylodis macrocephalae polysaccharides.

Auteurs : Wei Xu [République populaire de Chine] ; Sijia Fang [République populaire de Chine] ; Yong Wang [République populaire de Chine] ; Xiaoqing Chi [République populaire de Chine] ; Xiaodan Ma [République populaire de Chine] ; Tao Zhang [République populaire de Chine] ; Songhua Hu [République populaire de Chine]

Source :

RBID : pubmed:32070525

Descripteurs français

English descriptors

Abstract

The present study was to investigate the molecular mechanism underlying lymphocyte activation by total polysaccharides from Atractylodis macrocephalae (RAMPtp). The results showed that RAMPtp significantly promoted the secretions of cytokines (IFN-γ, IL-1α, IL-21, IFN-α, CCL4, CXCL9 and CXCL10), increased the proportions of CD4+ and CD8+ subpopulations, and enhanced the expressions of c-JUN, NFAT4, STAT1 and STAT3. microRNA sequencing identified 67 differentially expressed miRNAs (DEMs) in RAMPtp-stimulated SMLN lymphocytes, including 55 up-regulated and 12 down-regulated. GO and KEGG enrichment analyses of the predicted DEMs-targeted genes indicated that they were associated with immune system pathways, including PI3K-Akt, MAPKs, Jak-STAT and Calcium signaling pathways, which were confirmed by western blot and pathway inhibition assays. RAMPtp was further observed to favor immunostimulatory effect on both T and B lymphocytes via binding to TCR and membrane Ig individually. These findings might explain the immunomodulatory mechanism of RAMPtp in ameliorating the bovine intramammary infection.

DOI: 10.1016/j.carbpol.2020.115906
PubMed: 32070525


Affiliations:


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Le document en format XML

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<term>B-Lymphocytes (drug effects)</term>
<term>Cattle (MeSH)</term>
<term>Computational Biology (MeSH)</term>
<term>Cytokines (biosynthesis)</term>
<term>Lymphocyte Activation (drug effects)</term>
<term>Particle Size (MeSH)</term>
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<term>Animaux (MeSH)</term>
<term>Atractylodes (composition chimique)</term>
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<term>Bovins (MeSH)</term>
<term>Cytokines (biosynthèse)</term>
<term>Lymphocytes B (effets des médicaments et des substances chimiques)</term>
<term>Lymphocytes T (effets des médicaments et des substances chimiques)</term>
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<term>Polyosides (isolement et purification)</term>
<term>Polyosides (pharmacologie)</term>
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<div type="abstract" xml:lang="en">The present study was to investigate the molecular mechanism underlying lymphocyte activation by total polysaccharides from Atractylodis macrocephalae (RAMPtp). The results showed that RAMPtp significantly promoted the secretions of cytokines (IFN-γ, IL-1α, IL-21, IFN-α, CCL4, CXCL9 and CXCL10), increased the proportions of CD4
<sup>+</sup>
and CD8
<sup>+</sup>
subpopulations, and enhanced the expressions of c-JUN, NFAT4, STAT1 and STAT3. microRNA sequencing identified 67 differentially expressed miRNAs (DEMs) in RAMPtp-stimulated SMLN lymphocytes, including 55 up-regulated and 12 down-regulated. GO and KEGG enrichment analyses of the predicted DEMs-targeted genes indicated that they were associated with immune system pathways, including PI3K-Akt, MAPKs, Jak-STAT and Calcium signaling pathways, which were confirmed by western blot and pathway inhibition assays. RAMPtp was further observed to favor immunostimulatory effect on both T and B lymphocytes via binding to TCR and membrane Ig individually. These findings might explain the immunomodulatory mechanism of RAMPtp in ameliorating the bovine intramammary infection.</div>
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<AbstractText>The present study was to investigate the molecular mechanism underlying lymphocyte activation by total polysaccharides from Atractylodis macrocephalae (RAMPtp). The results showed that RAMPtp significantly promoted the secretions of cytokines (IFN-γ, IL-1α, IL-21, IFN-α, CCL4, CXCL9 and CXCL10), increased the proportions of CD4
<sup>+</sup>
and CD8
<sup>+</sup>
subpopulations, and enhanced the expressions of c-JUN, NFAT4, STAT1 and STAT3. microRNA sequencing identified 67 differentially expressed miRNAs (DEMs) in RAMPtp-stimulated SMLN lymphocytes, including 55 up-regulated and 12 down-regulated. GO and KEGG enrichment analyses of the predicted DEMs-targeted genes indicated that they were associated with immune system pathways, including PI3K-Akt, MAPKs, Jak-STAT and Calcium signaling pathways, which were confirmed by western blot and pathway inhibition assays. RAMPtp was further observed to favor immunostimulatory effect on both T and B lymphocytes via binding to TCR and membrane Ig individually. These findings might explain the immunomodulatory mechanism of RAMPtp in ameliorating the bovine intramammary infection.</AbstractText>
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<DescriptorName UI="D019295" MajorTopicYN="N">Computational Biology</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016207" MajorTopicYN="N">Cytokines</DescriptorName>
<QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008213" MajorTopicYN="N">Lymphocyte Activation</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010316" MajorTopicYN="N">Particle Size</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D011134" MajorTopicYN="N">Polysaccharides</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D015398" MajorTopicYN="N">Signal Transduction</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013499" MajorTopicYN="N">Surface Properties</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013601" MajorTopicYN="N">T-Lymphocytes</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D051197" MajorTopicYN="N">Toll-Like Receptor 4</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Atractylodis macrocephalae polysaccharides</Keyword>
<Keyword MajorTopicYN="N">Bovine lymphocytes</Keyword>
<Keyword MajorTopicYN="N">Immunomodulation</Keyword>
<Keyword MajorTopicYN="N">Receptor</Keyword>
<Keyword MajorTopicYN="N">Signaling pathway</Keyword>
<Keyword MajorTopicYN="N">miRNAs</Keyword>
</KeywordList>
<CoiStatement>Declaration of Competing Interest The authors declared no competing interests.</CoiStatement>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2019</Year>
<Month>11</Month>
<Day>07</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2019</Year>
<Month>12</Month>
<Day>30</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2020</Year>
<Month>01</Month>
<Day>20</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2020</Year>
<Month>2</Month>
<Day>20</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>2</Month>
<Day>20</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2020</Year>
<Month>10</Month>
<Day>22</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">32070525</ArticleId>
<ArticleId IdType="pii">S0144-8617(20)30080-1</ArticleId>
<ArticleId IdType="doi">10.1016/j.carbpol.2020.115906</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
</country>
<region>
<li>Zhejiang</li>
</region>
<settlement>
<li>Hangzhou</li>
</settlement>
<orgName>
<li>Université de Zhejiang</li>
</orgName>
</list>
<tree>
<country name="République populaire de Chine">
<region name="Zhejiang">
<name sortKey="Xu, Wei" sort="Xu, Wei" uniqKey="Xu W" first="Wei" last="Xu">Wei Xu</name>
</region>
<name sortKey="Chi, Xiaoqing" sort="Chi, Xiaoqing" uniqKey="Chi X" first="Xiaoqing" last="Chi">Xiaoqing Chi</name>
<name sortKey="Fang, Sijia" sort="Fang, Sijia" uniqKey="Fang S" first="Sijia" last="Fang">Sijia Fang</name>
<name sortKey="Hu, Songhua" sort="Hu, Songhua" uniqKey="Hu S" first="Songhua" last="Hu">Songhua Hu</name>
<name sortKey="Ma, Xiaodan" sort="Ma, Xiaodan" uniqKey="Ma X" first="Xiaodan" last="Ma">Xiaodan Ma</name>
<name sortKey="Wang, Yong" sort="Wang, Yong" uniqKey="Wang Y" first="Yong" last="Wang">Yong Wang</name>
<name sortKey="Zhang, Tao" sort="Zhang, Tao" uniqKey="Zhang T" first="Tao" last="Zhang">Tao Zhang</name>
</country>
</tree>
</affiliations>
</record>

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