http://purl.uniprot.org/citations/38194130 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/38194130 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundInterferon regulatory factors (IRF-1 and IRF-2) are transcription factors widely implicated in various cellular processes, including regulation of inflammatory responses to pathogens, cell proliferation, oncogenesis, differentiation, autophagy, and apoptosis.MethodsWe have studied the expression of IRF-1, IRF-2 mRNAs by RT-PCR, cellular localization of the proteins by immunofluorescence, and expression of mRNAs of genes regulated by IRF-1, IRF-2 by RT-PCR in mouse bone marrow cells (BMCs) and mesenchymal stem cells (MSCs).ResultsHigher level of IRF-1 mRNA was observed in BMCs and MSCs compared to that of IRF-2. Similarly, differential expression of IRF-1 and IRF-2 proteins was observed in BMCs and MSCs. IRF-1 was predominantly localized in the cytoplasm, whereas IRF-2 was localized in the nuclei of BMCs. MSCs showed nucleo-cytoplasmic distribution of IRF-1 and nuclear localization of IRF-2. Constitutive expression of IRF-1 and IRF-2 target genes: monocyte chemoattractant protein-1 (MCP-1), vascular cell adhesion molecule-1 (VCAM-1), cyclooxygenase-2 (COX-2), matrix metalloproteinase-9 (MMP-9), and caspase-1 was observed in both BMCs and MSCs. MSCs showed constitutive expression of the pluripotency-associated factors, Oct3/4 and Sox-2. Lipopolysaccharide (LPS)-treatment of MSCs induced prominent cellular localization of IRF-1 and IRF-2.ConclusionsOur results suggest that IRF-1 and IRF-2 exhibit differential expression of their mRNAs and subcellular localization of the proteins in BMCs and MSCs. These cells also show differential levels of constitutive expression of IRF-1 and IRF-2 target genes. This may regulate immune-responsive properties of BMCs and MSCs through IRF-1, IRF-2-dependent gene expression and protein-protein interaction. Regulating IRF-1 and IRF-2 may be helpful for immunomodulatory functions of MSCs for cell therapy and regenerative medicine."xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.org/dc/terms/identifier | "doi:10.1007/s11033-023-09025-9"xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/author | "Chaudhary J.K."xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/author | "Rath P.C."xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/author | "Ahamad N."xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/date | "2024"xsd:gYear |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/name | "Mol Biol Rep"xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/pages | "97"xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/title | "Mesenchymal stem cells (MSCs) from the mouse bone marrow show differential expression of interferon regulatory factors IRF-1 and IRF-2."xsd:string |
http://purl.uniprot.org/citations/38194130 | http://purl.uniprot.org/core/volume | "51"xsd:string |
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