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Hemangiosarcoma cells induce M2 polarization and PD-L1 expression in macrophages
Hemangiosarcoma (HSA) is a malignant tumor derived from endothelial cells. Tumor-associated macrophages are one of the major components of tumor microenvironment and crucial for cancer development. The presence and function of macrophages in HSA have not been studied because there is no syngeneic mo...
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Published in: | Scientific reports 2022-02, Vol.12 (1), p.2124-11, Article 2124 |
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description | Hemangiosarcoma (HSA) is a malignant tumor derived from endothelial cells. Tumor-associated macrophages are one of the major components of tumor microenvironment and crucial for cancer development. The presence and function of macrophages in HSA have not been studied because there is no syngeneic model for HSA. In this study, we evaluated two mouse HSA cell lines and one immortalized mouse endothelial cell line for their usefulness as syngeneic models for canine HSA. Our results showed that the ISOS-1 cell line developed tumors with similar morphology to canine HSA. ISOS-1 cells highly expressed KDM2B and had similar KDM2B target expression patterns with canine HSA. Moreover, we determined that in both ISOS-1 and canine HSA tumors, macrophages were present as a major constituent of the tumor microenvironment. These macrophages were positive for CD204, an M2 macrophage marker, and express PD-L1, an immune checkpoint molecule. Canine HSA with macrophages expressing PD-L1 had a smaller number of T-cells in tumor tissues than tumors with PD-L1 negative macrophages. ISOS-1-conditioned medium could induce M2 polarization and PD-L1 expression in RAW264.7 mouse macrophage cell line and mouse peritoneal macrophages. These results show that ISOS-1 can be used as a syngenic model for canine HSA and suggest that macrophages play an important role in immune evasion in HSA. Using the syngeneic mouse model for canine HSA, we can further study the role of immune cells in the pathology of HSA. |
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Tumor-associated macrophages are one of the major components of tumor microenvironment and crucial for cancer development. The presence and function of macrophages in HSA have not been studied because there is no syngeneic model for HSA. In this study, we evaluated two mouse HSA cell lines and one immortalized mouse endothelial cell line for their usefulness as syngeneic models for canine HSA. Our results showed that the ISOS-1 cell line developed tumors with similar morphology to canine HSA. ISOS-1 cells highly expressed KDM2B and had similar KDM2B target expression patterns with canine HSA. Moreover, we determined that in both ISOS-1 and canine HSA tumors, macrophages were present as a major constituent of the tumor microenvironment. These macrophages were positive for CD204, an M2 macrophage marker, and express PD-L1, an immune checkpoint molecule. Canine HSA with macrophages expressing PD-L1 had a smaller number of T-cells in tumor tissues than tumors with PD-L1 negative macrophages. ISOS-1-conditioned medium could induce M2 polarization and PD-L1 expression in RAW264.7 mouse macrophage cell line and mouse peritoneal macrophages. These results show that ISOS-1 can be used as a syngenic model for canine HSA and suggest that macrophages play an important role in immune evasion in HSA. Using the syngeneic mouse model for canine HSA, we can further study the role of immune cells in the pathology of HSA.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-022-06203-w</identifier><identifier>PMID: 35136176</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1798 ; 692/308/1426 ; Animal models ; Animals ; Cell Line, Tumor ; Cytology ; Dogs ; Endothelial cells ; Hemangiosarcoma - immunology ; Hemangiosarcoma - veterinary ; Humanities and Social Sciences ; Immune checkpoint ; Lymphocytes T ; Macrophages ; Macrophages - physiology ; Mice ; multidisciplinary ; PD-L1 protein ; Polarization ; Science ; Science (multidisciplinary) ; Splenic Neoplasms - immunology ; Splenic Neoplasms - veterinary ; Tumor Escape ; Tumor Microenvironment ; Tumors</subject><ispartof>Scientific reports, 2022-02, Vol.12 (1), p.2124-11, Article 2124</ispartof><rights>The Author(s) 2022</rights><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c650t-77038be8fdf84476653df7b868370f22cb48d11e56216f1a01a9c4414ec2efd43</citedby><cites>FETCH-LOGICAL-c650t-77038be8fdf84476653df7b868370f22cb48d11e56216f1a01a9c4414ec2efd43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2626565375/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2626565375?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35136176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gulay, Kevin Christian M.</creatorcontrib><creatorcontrib>Aoshima, Keisuke</creatorcontrib><creatorcontrib>Maekawa, Naoya</creatorcontrib><creatorcontrib>Suzuki, Tamami</creatorcontrib><creatorcontrib>Konnai, Satoru</creatorcontrib><creatorcontrib>Kobayashi, Atsushi</creatorcontrib><creatorcontrib>Kimura, Takashi</creatorcontrib><title>Hemangiosarcoma cells induce M2 polarization and PD-L1 expression in macrophages</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Hemangiosarcoma (HSA) is a malignant tumor derived from endothelial cells. 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Canine HSA with macrophages expressing PD-L1 had a smaller number of T-cells in tumor tissues than tumors with PD-L1 negative macrophages. ISOS-1-conditioned medium could induce M2 polarization and PD-L1 expression in RAW264.7 mouse macrophage cell line and mouse peritoneal macrophages. These results show that ISOS-1 can be used as a syngenic model for canine HSA and suggest that macrophages play an important role in immune evasion in HSA. 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Tumor-associated macrophages are one of the major components of tumor microenvironment and crucial for cancer development. The presence and function of macrophages in HSA have not been studied because there is no syngeneic model for HSA. In this study, we evaluated two mouse HSA cell lines and one immortalized mouse endothelial cell line for their usefulness as syngeneic models for canine HSA. Our results showed that the ISOS-1 cell line developed tumors with similar morphology to canine HSA. ISOS-1 cells highly expressed KDM2B and had similar KDM2B target expression patterns with canine HSA. Moreover, we determined that in both ISOS-1 and canine HSA tumors, macrophages were present as a major constituent of the tumor microenvironment. These macrophages were positive for CD204, an M2 macrophage marker, and express PD-L1, an immune checkpoint molecule. Canine HSA with macrophages expressing PD-L1 had a smaller number of T-cells in tumor tissues than tumors with PD-L1 negative macrophages. ISOS-1-conditioned medium could induce M2 polarization and PD-L1 expression in RAW264.7 mouse macrophage cell line and mouse peritoneal macrophages. These results show that ISOS-1 can be used as a syngenic model for canine HSA and suggest that macrophages play an important role in immune evasion in HSA. Using the syngeneic mouse model for canine HSA, we can further study the role of immune cells in the pathology of HSA.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>35136176</pmid><doi>10.1038/s41598-022-06203-w</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/67/1798 692/308/1426 Animal models Animals Cell Line, Tumor Cytology Dogs Endothelial cells Hemangiosarcoma - immunology Hemangiosarcoma - veterinary Humanities and Social Sciences Immune checkpoint Lymphocytes T Macrophages Macrophages - physiology Mice multidisciplinary PD-L1 protein Polarization Science Science (multidisciplinary) Splenic Neoplasms - immunology Splenic Neoplasms - veterinary Tumor Escape Tumor Microenvironment Tumors |
title | Hemangiosarcoma cells induce M2 polarization and PD-L1 expression in macrophages |
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