Glutathione S -transferases promote proinflammatory astrocyte-microglia communication during brain inflammation
Astrocytes and microglia play critical roles in brain inflammation. Here, we report that glutathione -transferases (GSTs), particularly GSTM1, promote proinflammatory signaling in astrocytes and contribute to astrocyte-mediated microglia activation during brain inflammation. In vivo, astrocyte-speci...
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Veröffentlicht in: | Science signaling 2019-02, Vol.12 (569) |
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creator | Kano, Shin-Ichi Choi, Eric Y Dohi, Eisuke Agarwal, Swati Chang, Daniel J Wilson, Ashley M Lo, Brian D Rose, Indigo V L Gonzalez, Santiago Imai, Takashi Sawa, Akira |
description | Astrocytes and microglia play critical roles in brain inflammation. Here, we report that glutathione
-transferases (GSTs), particularly GSTM1, promote proinflammatory signaling in astrocytes and contribute to astrocyte-mediated microglia activation during brain inflammation. In vivo, astrocyte-specific knockdown of GSTM1 in the prefrontal cortex attenuated microglia activation in brain inflammation induced by systemic injection of lipopolysaccharides (LPS). Knocking down GSTM1 in astrocytes also attenuated LPS-induced production of the proinflammatory cytokine tumor necrosis factor-α (TNF-α) by microglia when the two cell types were cocultured. In astrocytes, GSTM1 was required for the activation of nuclear factor κB (NF-κB) and the production of proinflammatory mediators, such as granulocyte-macrophage colony-stimulating factor (GM-CSF) and C-C motif chemokine ligand 2 (CCL2), both of which enhance microglia activation. Our study suggests that GSTs play a proinflammatory role in priming astrocytes and enhancing microglia activation in a microglia-astrocyte positive feedback loop during brain inflammation. |
doi_str_mv | 10.1126/scisignal.aar2124 |
format | Article |
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-transferases (GSTs), particularly GSTM1, promote proinflammatory signaling in astrocytes and contribute to astrocyte-mediated microglia activation during brain inflammation. In vivo, astrocyte-specific knockdown of GSTM1 in the prefrontal cortex attenuated microglia activation in brain inflammation induced by systemic injection of lipopolysaccharides (LPS). Knocking down GSTM1 in astrocytes also attenuated LPS-induced production of the proinflammatory cytokine tumor necrosis factor-α (TNF-α) by microglia when the two cell types were cocultured. In astrocytes, GSTM1 was required for the activation of nuclear factor κB (NF-κB) and the production of proinflammatory mediators, such as granulocyte-macrophage colony-stimulating factor (GM-CSF) and C-C motif chemokine ligand 2 (CCL2), both of which enhance microglia activation. Our study suggests that GSTs play a proinflammatory role in priming astrocytes and enhancing microglia activation in a microglia-astrocyte positive feedback loop during brain inflammation.</description><identifier>ISSN: 1945-0877</identifier><identifier>EISSN: 1937-9145</identifier><identifier>DOI: 10.1126/scisignal.aar2124</identifier><identifier>PMID: 30783009</identifier><language>eng</language><publisher>United States: The American Association for the Advancement of Science</publisher><subject>Activation ; Animals ; Animals, Newborn ; Astrocytes ; Astrocytes - cytology ; Astrocytes - metabolism ; Brain ; Cells, Cultured ; Cerebrospinal fluid ; Chemokines ; Coculture Techniques ; Colony-stimulating factor ; Cytokines - genetics ; Cytokines - metabolism ; Encephalitis - genetics ; Encephalitis - metabolism ; Encephalitis - pathology ; Feedback loops ; Female ; Glutathione ; Glutathione Transferase - genetics ; Glutathione Transferase - metabolism ; Granulocyte-macrophage colony stimulating factor ; GSTM1 protein ; HEK293 Cells ; Humans ; Inflammation ; Lipopolysaccharides ; Lipopolysaccharides - pharmacology ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Microglia ; Microglia - cytology ; Microglia - metabolism ; Monocyte chemoattractant protein 1 ; NF-κB protein ; Positive feedback ; Prefrontal cortex ; Priming ; RNA Interference ; Signal Transduction - drug effects ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α ; Vaccines</subject><ispartof>Science signaling, 2019-02, Vol.12 (569)</ispartof><rights>Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.</rights><rights>Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-92c7f6726d204cbf15be3c9781e6d5a6ce320fb46331416e0f2f1ede02d728683</citedby><cites>FETCH-LOGICAL-c427t-92c7f6726d204cbf15be3c9781e6d5a6ce320fb46331416e0f2f1ede02d728683</cites><orcidid>0000-0001-9049-8102 ; 0000-0002-5171-3436 ; 0000-0003-3991-7978 ; 0000-0002-5365-4900 ; 0000-0002-9389-3658 ; 0000-0002-1762-6670</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,2885,2886,27925,27926</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30783009$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kano, Shin-Ichi</creatorcontrib><creatorcontrib>Choi, Eric Y</creatorcontrib><creatorcontrib>Dohi, Eisuke</creatorcontrib><creatorcontrib>Agarwal, Swati</creatorcontrib><creatorcontrib>Chang, Daniel J</creatorcontrib><creatorcontrib>Wilson, Ashley M</creatorcontrib><creatorcontrib>Lo, Brian D</creatorcontrib><creatorcontrib>Rose, Indigo V L</creatorcontrib><creatorcontrib>Gonzalez, Santiago</creatorcontrib><creatorcontrib>Imai, Takashi</creatorcontrib><creatorcontrib>Sawa, Akira</creatorcontrib><title>Glutathione S -transferases promote proinflammatory astrocyte-microglia communication during brain inflammation</title><title>Science signaling</title><addtitle>Sci Signal</addtitle><description>Astrocytes and microglia play critical roles in brain inflammation. Here, we report that glutathione
-transferases (GSTs), particularly GSTM1, promote proinflammatory signaling in astrocytes and contribute to astrocyte-mediated microglia activation during brain inflammation. In vivo, astrocyte-specific knockdown of GSTM1 in the prefrontal cortex attenuated microglia activation in brain inflammation induced by systemic injection of lipopolysaccharides (LPS). Knocking down GSTM1 in astrocytes also attenuated LPS-induced production of the proinflammatory cytokine tumor necrosis factor-α (TNF-α) by microglia when the two cell types were cocultured. In astrocytes, GSTM1 was required for the activation of nuclear factor κB (NF-κB) and the production of proinflammatory mediators, such as granulocyte-macrophage colony-stimulating factor (GM-CSF) and C-C motif chemokine ligand 2 (CCL2), both of which enhance microglia activation. Our study suggests that GSTs play a proinflammatory role in priming astrocytes and enhancing microglia activation in a microglia-astrocyte positive feedback loop during brain inflammation.</description><subject>Activation</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Astrocytes</subject><subject>Astrocytes - cytology</subject><subject>Astrocytes - metabolism</subject><subject>Brain</subject><subject>Cells, Cultured</subject><subject>Cerebrospinal fluid</subject><subject>Chemokines</subject><subject>Coculture Techniques</subject><subject>Colony-stimulating factor</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>Encephalitis - genetics</subject><subject>Encephalitis - metabolism</subject><subject>Encephalitis - pathology</subject><subject>Feedback loops</subject><subject>Female</subject><subject>Glutathione</subject><subject>Glutathione Transferase - genetics</subject><subject>Glutathione Transferase - metabolism</subject><subject>Granulocyte-macrophage colony stimulating factor</subject><subject>GSTM1 protein</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Microglia</subject><subject>Microglia - cytology</subject><subject>Microglia - metabolism</subject><subject>Monocyte chemoattractant protein 1</subject><subject>NF-κB protein</subject><subject>Positive feedback</subject><subject>Prefrontal cortex</subject><subject>Priming</subject><subject>RNA Interference</subject><subject>Signal Transduction - drug effects</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><subject>Vaccines</subject><issn>1945-0877</issn><issn>1937-9145</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU9P3DAQxa2qqFDoB-ilitRLLwH_i51ckBBqKRISB-BsOc54MYrtre1U2m-Pt7tdtZzG0rz3PDM_hD4TfE4IFRfZuOxWQc_nWidKKH-HTsjAZDsQ3r3fvnnX4l7KY_Qx5xeMBaF0-ICOGZY9w3g4QfFmXoouzy4GaB6atiQdsoWkM-RmnaKPBbbVBTtr73WJadPoXFI0mwKtdybF1ex0Y6L3S3BGlxrVTEtyYdWMSbvQHLy1c4aOrJ4zfNrXU_T04_vj9c_27v7m9vrqrjWcytIO1EgrJBUTxdyMlnQjMDPInoCYOi0MMIrtyAVjhBMB2FJLYAJMJ0l70bNTdLnLXS-jh8lAqJvNap2c12mjonbq_05wz2oVfyshmCSC14Bv-4AUfy2Qi_IuG5hnHSAuWVHSc1Jn_fPX1zfSl7ikimWn6jgXXVdVZKeqF8s5gT0MQ7Da4lQHnGqPs3q-_LvFwfGXH3sF7dOi5Q</recordid><startdate>20190219</startdate><enddate>20190219</enddate><creator>Kano, Shin-Ichi</creator><creator>Choi, Eric Y</creator><creator>Dohi, Eisuke</creator><creator>Agarwal, Swati</creator><creator>Chang, Daniel J</creator><creator>Wilson, Ashley M</creator><creator>Lo, Brian D</creator><creator>Rose, Indigo V L</creator><creator>Gonzalez, Santiago</creator><creator>Imai, Takashi</creator><creator>Sawa, Akira</creator><general>The American Association for the Advancement of Science</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JQ2</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9049-8102</orcidid><orcidid>https://orcid.org/0000-0002-5171-3436</orcidid><orcidid>https://orcid.org/0000-0003-3991-7978</orcidid><orcidid>https://orcid.org/0000-0002-5365-4900</orcidid><orcidid>https://orcid.org/0000-0002-9389-3658</orcidid><orcidid>https://orcid.org/0000-0002-1762-6670</orcidid></search><sort><creationdate>20190219</creationdate><title>Glutathione S -transferases promote proinflammatory astrocyte-microglia communication during brain inflammation</title><author>Kano, Shin-Ichi ; Choi, Eric Y ; Dohi, Eisuke ; Agarwal, Swati ; Chang, Daniel J ; Wilson, Ashley M ; Lo, Brian D ; Rose, Indigo V L ; Gonzalez, Santiago ; Imai, Takashi ; Sawa, Akira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-92c7f6726d204cbf15be3c9781e6d5a6ce320fb46331416e0f2f1ede02d728683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Activation</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Astrocytes</topic><topic>Astrocytes - cytology</topic><topic>Astrocytes - metabolism</topic><topic>Brain</topic><topic>Cells, Cultured</topic><topic>Cerebrospinal fluid</topic><topic>Chemokines</topic><topic>Coculture Techniques</topic><topic>Colony-stimulating factor</topic><topic>Cytokines - genetics</topic><topic>Cytokines - metabolism</topic><topic>Encephalitis - genetics</topic><topic>Encephalitis - metabolism</topic><topic>Encephalitis - pathology</topic><topic>Feedback loops</topic><topic>Female</topic><topic>Glutathione</topic><topic>Glutathione Transferase - genetics</topic><topic>Glutathione Transferase - metabolism</topic><topic>Granulocyte-macrophage colony stimulating factor</topic><topic>GSTM1 protein</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Lipopolysaccharides</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Microglia</topic><topic>Microglia - cytology</topic><topic>Microglia - metabolism</topic><topic>Monocyte chemoattractant protein 1</topic><topic>NF-κB protein</topic><topic>Positive feedback</topic><topic>Prefrontal cortex</topic><topic>Priming</topic><topic>RNA Interference</topic><topic>Signal Transduction - drug effects</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kano, Shin-Ichi</creatorcontrib><creatorcontrib>Choi, Eric Y</creatorcontrib><creatorcontrib>Dohi, Eisuke</creatorcontrib><creatorcontrib>Agarwal, Swati</creatorcontrib><creatorcontrib>Chang, Daniel J</creatorcontrib><creatorcontrib>Wilson, Ashley M</creatorcontrib><creatorcontrib>Lo, Brian D</creatorcontrib><creatorcontrib>Rose, Indigo V L</creatorcontrib><creatorcontrib>Gonzalez, Santiago</creatorcontrib><creatorcontrib>Imai, Takashi</creatorcontrib><creatorcontrib>Sawa, Akira</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Science signaling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kano, Shin-Ichi</au><au>Choi, Eric Y</au><au>Dohi, Eisuke</au><au>Agarwal, Swati</au><au>Chang, Daniel J</au><au>Wilson, Ashley M</au><au>Lo, Brian D</au><au>Rose, Indigo V L</au><au>Gonzalez, Santiago</au><au>Imai, Takashi</au><au>Sawa, Akira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glutathione S -transferases promote proinflammatory astrocyte-microglia communication during brain inflammation</atitle><jtitle>Science signaling</jtitle><addtitle>Sci Signal</addtitle><date>2019-02-19</date><risdate>2019</risdate><volume>12</volume><issue>569</issue><issn>1945-0877</issn><eissn>1937-9145</eissn><abstract>Astrocytes and microglia play critical roles in brain inflammation. Here, we report that glutathione
-transferases (GSTs), particularly GSTM1, promote proinflammatory signaling in astrocytes and contribute to astrocyte-mediated microglia activation during brain inflammation. In vivo, astrocyte-specific knockdown of GSTM1 in the prefrontal cortex attenuated microglia activation in brain inflammation induced by systemic injection of lipopolysaccharides (LPS). Knocking down GSTM1 in astrocytes also attenuated LPS-induced production of the proinflammatory cytokine tumor necrosis factor-α (TNF-α) by microglia when the two cell types were cocultured. In astrocytes, GSTM1 was required for the activation of nuclear factor κB (NF-κB) and the production of proinflammatory mediators, such as granulocyte-macrophage colony-stimulating factor (GM-CSF) and C-C motif chemokine ligand 2 (CCL2), both of which enhance microglia activation. Our study suggests that GSTs play a proinflammatory role in priming astrocytes and enhancing microglia activation in a microglia-astrocyte positive feedback loop during brain inflammation.</abstract><cop>United States</cop><pub>The American Association for the Advancement of Science</pub><pmid>30783009</pmid><doi>10.1126/scisignal.aar2124</doi><orcidid>https://orcid.org/0000-0001-9049-8102</orcidid><orcidid>https://orcid.org/0000-0002-5171-3436</orcidid><orcidid>https://orcid.org/0000-0003-3991-7978</orcidid><orcidid>https://orcid.org/0000-0002-5365-4900</orcidid><orcidid>https://orcid.org/0000-0002-9389-3658</orcidid><orcidid>https://orcid.org/0000-0002-1762-6670</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Activation Animals Animals, Newborn Astrocytes Astrocytes - cytology Astrocytes - metabolism Brain Cells, Cultured Cerebrospinal fluid Chemokines Coculture Techniques Colony-stimulating factor Cytokines - genetics Cytokines - metabolism Encephalitis - genetics Encephalitis - metabolism Encephalitis - pathology Feedback loops Female Glutathione Glutathione Transferase - genetics Glutathione Transferase - metabolism Granulocyte-macrophage colony stimulating factor GSTM1 protein HEK293 Cells Humans Inflammation Lipopolysaccharides Lipopolysaccharides - pharmacology Male Mice, Inbred C57BL Mice, Knockout Mice, Transgenic Microglia Microglia - cytology Microglia - metabolism Monocyte chemoattractant protein 1 NF-κB protein Positive feedback Prefrontal cortex Priming RNA Interference Signal Transduction - drug effects Tumor necrosis factor-TNF Tumor necrosis factor-α Vaccines |
title | Glutathione S -transferases promote proinflammatory astrocyte-microglia communication during brain inflammation |
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