Hyaluronic acid-based extracellular matrix triggers spontaneous M2-like polarity of monocyte/macrophage

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dc.contributor.authorKim, Hyebinko
dc.contributor.authorCha, Junghwako
dc.contributor.authorJang, Minjeongko
dc.contributor.authorKim, Pilnamko
dc.date.accessioned2019-07-23T06:21:23Z-
dc.date.available2019-07-23T06:21:23Z-
dc.date.created2019-07-23-
dc.date.created2019-07-23-
dc.date.issued2019-06-
dc.identifier.citationBIOMATERIALS SCIENCE, v.7, no.6, pp.2264 - 2271-
dc.identifier.issn2047-4830-
dc.identifier.urihttp://hdl.handle.net/10203/263749-
dc.description.abstractHyaluronic acid (HA) is found in various tumor tissues, and is considered tumor-associated extracellular matrix (ECM). Within this tumor-associated ECM, stromal cells, especially immune cells, are involved in tumor progression. However, the effects of tumor-associated ECM on the characteristics of immune cells remain unexplored. Therefore, we studied the triggering effect of HA on spontaneous M2-like polarity of monocytes/macrophages using HA-mixed collagen (HA-COL) matrix. In the presence of HA, expression of the HA receptor (CD44) and M2 polarity-related genes was upregulated in human monocytes (THP-1 cells). We confirmed the CD44-mediated activation of STAT3 in THP-1 cells cultured in an HA-rich environment. Furthermore, when we induced the THP-1 cells to differentiate into cells with M1 or M2 polarity within an HA-rich environment, the HA-rich environment influenced the direction of induction. Our findings might improve understanding of the crosstalk between immune cells and tumor-associated ECM, and facilitate development of tumor immunotherapy strategies.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleHyaluronic acid-based extracellular matrix triggers spontaneous M2-like polarity of monocyte/macrophage-
dc.typeArticle-
dc.identifier.wosid000474065900003-
dc.identifier.scopusid2-s2.0-85066633424-
dc.type.rimsART-
dc.citation.volume7-
dc.citation.issue6-
dc.citation.beginningpage2264-
dc.citation.endingpage2271-
dc.citation.publicationnameBIOMATERIALS SCIENCE-
dc.identifier.doi10.1039/c9bm00155g-
dc.contributor.localauthorKim, Pilnam-
dc.contributor.nonIdAuthorKim, Hyebin-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusTUMOR-ASSOCIATED MACROPHAGES-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusRECEPTORS-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusCD44-
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