Lahaye, Clement et al. published their research in Journal of Trace Elements in Medicine and Biology in 2021 |CAS: 2358-84-1

The Article related to human iron overload metabolic syndrome macrophage polarization, dysmetabolic iron overload syndrome, ferritin, inflammation, macrophage polarization, metabolic syndrome, Placeholder for records without volume info and other aspects.Category: esters-buliding-blocks

On September 30, 2021, Lahaye, Clement; Gladine, Cecile; Pereira, Bruno; Berger, Juliette; Chinetti-Gbaguidi, Giulia; Laine, Fabrice; Mazur, Andrzej; Ruivard, Marc published an article.Category: esters-buliding-blocks The title of the article was Does iron overload in metabolic syndrome affect macrophage profile? A case control study. And the article contained the following:

Dysmetabolic iron overload syndrome (DIOS) is common but the clin. relevance of iron overload is not understood. Macrophages are central cells in iron homeostasis and inflammation. We hypothesized that iron overload in DIOS could affect the phenotype of monocytes and impair macrophage gene expression. This study compared 20 subjects with DIOS to 20 subjects with metabolic syndrome (MetS) without iron overload, and 20 healthy controls. Monocytes were phenotyped by Fluorescence-Activated Cell Sorting (FACS) and differentiated into anti-inflammatory M2 macrophages in the presence of IL-4. The expression of 38 genes related to inflammation, iron metabolism and M2 phenotype was assessed by real-time PCR. FACS showed no difference between monocytes across the three groups. The macrophagic response to IL-4-driven differentiation was altered in four of the five genes of M2 phenotype (MRC1, F13A1, ABCA1, TGM2 but not FABP4), in DIOS vs Mets and controls demonstrating an impaired M2 polarization. The expression profile of inflammatory genes was not different in DIOS vs MetS. Several genes of iron metabolism presented a higher expression in DIOS vs MetS: SCL11A2 (a free iron transporter, +76%, p = 0.04), SOD1 (an antioxidant enzyme, +27%, p = 0.02), and TFRC (the receptor 1 of transferrin, +59%, p = 0.003). In DIOS, macrophage polarization toward the M2 alternative phenotype is impaired but not associated with a pro-inflammatory profile. The up regulation of transferrin receptor 1 (TFRC) in DIOS macrophages suggests an adaptive role that may limit iron toxicity in DIOS. The experimental process involved the reaction of Oxybis(ethane-2,1-diyl) bis(2-methylacrylate)(cas: 2358-84-1).Category: esters-buliding-blocks

The Article related to human iron overload metabolic syndrome macrophage polarization, dysmetabolic iron overload syndrome, ferritin, inflammation, macrophage polarization, metabolic syndrome, Placeholder for records without volume info and other aspects.Category: esters-buliding-blocks

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