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J Exp Med ; 215(11): 2725-2736, 2018 11 05.
Article in English | MEDLINE | ID: mdl-30355614

ABSTRACT

Monocytes are crucial immune cells involved in regulation of inflammation either directly or via differentiation into macrophages in tissues. However, many aspects of how their function is controlled in health and disease are not understood. Here we show that human blood monocytes activate high levels of the cytokine TGFß, a pathway that is not evident in mouse monocytes. Human CD14+, but not CD16+, monocytes activate TGFß via expression of the integrin αvß8 and matrix metalloproteinase 14, which dampens their production of TNFα in response to LPS. Additionally, when monocytes differentiate into macrophages, integrin expression and TGFß-activating ability are maintained in anti-inflammatory macrophages but down-regulated in pro-inflammatory macrophages. In the healthy human intestine, integrin αvß8 is highly expressed on mature tissue macrophages, with these cells and their integrin expression being significantly reduced in active inflammatory bowel disease. Thus, our data suggest that integrin αvß8-mediated TGFß activation plays a key role in regulation of monocyte inflammatory responses and intestinal macrophage homeostasis.


Subject(s)
Immune Tolerance , Inflammatory Bowel Diseases/immunology , Integrins/immunology , Macrophages/immunology , Monocytes/immunology , Transforming Growth Factor beta/immunology , Adolescent , Adult , Aged , Female , Humans , Inflammatory Bowel Diseases/pathology , Intestines/immunology , Intestines/pathology , Macrophages/pathology , Male , Middle Aged , Monocytes/pathology , Tumor Necrosis Factor-alpha/immunology
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