Matches in SemOpenAlex for { <https://semopenalex.org/work/W2080360768> ?p ?o ?g. }
- W2080360768 endingPage "1753" @default.
- W2080360768 startingPage "1733" @default.
- W2080360768 abstract "In vivo, cytokines noncovalently bind to the extracellular matrix (ECM), to facilitate intimate interactions with cellular receptors and potentiate biological activity. Development of a biomaterial that simulates this type of physiological binding and function is an exciting proposition for designing controlled advanced delivery systems for simulating in vivo conditions in vitro. We have decorated silk protein with sulfonated moieties through diazonium coupling reactions to noncovalently immobilize pro-inflammatory cytokines interleukin-1 beta (IL-1β) and tumor necrosis factor alpha (TNF-α) in such a biomimetic manner. After adsorption of the cytokines to the diazonium-modified silk matrix, constant release of cytokines up to at least 3 days was demonstrated, as an initial step to simulate an osteoarthritic (OA) microenvironment in vitro. Matrix-embedded cytokines induced the formation of multiple elongated processes in chondrocytes in vitro, akin to what is seen in OA cartilage in vivo. Gene expression profiles with this in vitro tissue model of OA showed significant similarities to profiles from explanted OA cartilage tissues collected from patients who underwent total knee replacement surgery. The common markers of OA, including COL, MMP, TIMP, ADAMTS, and metallothioneins, were upregulated at least 35-fold in the in vitro model when compared to the control-non-OA in vitro generated tissue-engineered cartilage. The microarray data were validated by reverse transcriptase-polymerase chain reaction. Mechanistically, protein interaction studies indicated that TNF-α and IL-1β synergistically controlled the equilibrium between MMPs and their inhibitors, TIMPs, resulting in ECM degradation through the MAPK pathway. This study offers a promising initial step toward establishing a relevant in vitro OA disease model, which can be further modified to assess signaling mechanisms, responses to cell or drug treatments and patient-specific features." @default.
- W2080360768 created "2016-06-24" @default.
- W2080360768 creator A5017091864 @default.
- W2080360768 creator A5022586568 @default.
- W2080360768 creator A5023614019 @default.
- W2080360768 creator A5034475246 @default.
- W2080360768 creator A5057871048 @default.
- W2080360768 creator A5072250764 @default.
- W2080360768 date "2013-08-01" @default.
- W2080360768 modified "2023-09-27" @default.
- W2080360768 title "Matrix-Embedded Cytokines to Simulate Osteoarthritis-Like Cartilage Microenvironments" @default.
- W2080360768 cites W1486180443 @default.
- W2080360768 cites W1605399752 @default.
- W2080360768 cites W1812173421 @default.
- W2080360768 cites W1971180693 @default.
- W2080360768 cites W1974873948 @default.
- W2080360768 cites W1976906604 @default.
- W2080360768 cites W1978772096 @default.
- W2080360768 cites W1984602372 @default.
- W2080360768 cites W1989045284 @default.
- W2080360768 cites W1990255645 @default.
- W2080360768 cites W1997669605 @default.
- W2080360768 cites W2002554431 @default.
- W2080360768 cites W2002963723 @default.
- W2080360768 cites W2004151551 @default.
- W2080360768 cites W2007470352 @default.
- W2080360768 cites W2009524387 @default.
- W2080360768 cites W2023669928 @default.
- W2080360768 cites W2024890586 @default.
- W2080360768 cites W2026245214 @default.
- W2080360768 cites W2029620160 @default.
- W2080360768 cites W2033592937 @default.
- W2080360768 cites W2042604054 @default.
- W2080360768 cites W2047703526 @default.
- W2080360768 cites W2059842158 @default.
- W2080360768 cites W2062522737 @default.
- W2080360768 cites W2062676485 @default.
- W2080360768 cites W2063045388 @default.
- W2080360768 cites W2066260702 @default.
- W2080360768 cites W2067853347 @default.
- W2080360768 cites W2067870418 @default.
- W2080360768 cites W2068864388 @default.
- W2080360768 cites W2070105244 @default.
- W2080360768 cites W2074549189 @default.
- W2080360768 cites W2074619002 @default.
- W2080360768 cites W2074676443 @default.
- W2080360768 cites W2074689848 @default.
- W2080360768 cites W2077766596 @default.
- W2080360768 cites W2078971015 @default.
- W2080360768 cites W2084368833 @default.
- W2080360768 cites W2084843851 @default.
- W2080360768 cites W2090748712 @default.
- W2080360768 cites W2091447263 @default.
- W2080360768 cites W2095319778 @default.
- W2080360768 cites W2101276590 @default.
- W2080360768 cites W2103919594 @default.
- W2080360768 cites W2109142422 @default.
- W2080360768 cites W2127940908 @default.
- W2080360768 cites W2129993616 @default.
- W2080360768 cites W2133465414 @default.
- W2080360768 cites W2135482856 @default.
- W2080360768 cites W2145506897 @default.
- W2080360768 cites W2145684243 @default.
- W2080360768 cites W2153192975 @default.
- W2080360768 cites W2155145299 @default.
- W2080360768 cites W2158305254 @default.
- W2080360768 cites W2160964180 @default.
- W2080360768 cites W2164982699 @default.
- W2080360768 cites W2167037356 @default.
- W2080360768 cites W2567898504 @default.
- W2080360768 cites W89635294 @default.
- W2080360768 doi "https://doi.org/10.1089/ten.tea.2012.0385" @default.
- W2080360768 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3700141" @default.
- W2080360768 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23470228" @default.
- W2080360768 hasPublicationYear "2013" @default.
- W2080360768 type Work @default.
- W2080360768 sameAs 2080360768 @default.
- W2080360768 citedByCount "35" @default.
- W2080360768 countsByYear W20803607682014 @default.
- W2080360768 countsByYear W20803607682015 @default.
- W2080360768 countsByYear W20803607682016 @default.
- W2080360768 countsByYear W20803607682017 @default.
- W2080360768 countsByYear W20803607682018 @default.
- W2080360768 countsByYear W20803607682019 @default.
- W2080360768 countsByYear W20803607682020 @default.
- W2080360768 countsByYear W20803607682021 @default.
- W2080360768 countsByYear W20803607682022 @default.
- W2080360768 countsByYear W20803607682023 @default.
- W2080360768 crossrefType "journal-article" @default.
- W2080360768 hasAuthorship W2080360768A5017091864 @default.
- W2080360768 hasAuthorship W2080360768A5022586568 @default.
- W2080360768 hasAuthorship W2080360768A5023614019 @default.
- W2080360768 hasAuthorship W2080360768A5034475246 @default.
- W2080360768 hasAuthorship W2080360768A5057871048 @default.
- W2080360768 hasAuthorship W2080360768A5072250764 @default.
- W2080360768 hasBestOaLocation W20803607682 @default.
- W2080360768 hasConcept C105702510 @default.
- W2080360768 hasConcept C106487976 @default.