2013
DOI: 10.1016/j.imlet.2013.01.007
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Intestinal dendritic cells: Their role in intestinal inflammation, manipulation by the gut microbiota and differences between mice and men

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Cited by 88 publications
(93 citation statements)
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“…85,107,118,[202][203][204][205] However many phenotypic markers of the myeloid lineage including CD11b, F4/80 and CD11c…”
Section: Human Intestinal Macrophagesmentioning
confidence: 99%
See 1 more Smart Citation
“…85,107,118,[202][203][204][205] However many phenotypic markers of the myeloid lineage including CD11b, F4/80 and CD11c…”
Section: Human Intestinal Macrophagesmentioning
confidence: 99%
“…5 CD163 or CD206 are also expressed by most mature m in humans, but they express low amounts of CD14, which is found at high levels on classical monocytes and immature m . 85,107,118,[202][203][204][205] Using markers of this kind, it can be shown that a monocyte-m "waterfall" 142 Indeed, there appear to be several differences in how responsiveness to pattern recognition receptors is regulated in human and murine m in general. 206 As in mice however, IL-10 plays an essential role in controlling the pro-inflammatory potential of human intestinal m and non-functional mutations in the IL-10R lead to severe, early onset IBD.…”
Section: Human Intestinal Macrophagesmentioning
confidence: 99%
“…In the proximal gut segments, even under homeostasis, where the microbiota is rare, some commensal bacteria can be in close contact with the epithelial cells. The IS scavenges these bacteria and generates primary T-cell responses, either immunogenic or tolerogenic (24). However, this concept, validated in healthy subjects and in patients with inflammatory bowel disease, has to be reconsidered in metabolic diseases, because gut dysbiosis can be induced within a few days or weeks by a diet change (25), allowing pathogens to penetrate the body without being destroyed by the innate and specific adaptive ISs, through a nucleotide-binding oligomerization domain 1-and LPS-cluster of differentiation 14-dependent translocation mechanism, which, when hampered, improves insulin sensitivity (26).…”
mentioning
confidence: 99%
“…Interestingly, however, the expression of CX3CR1 + in macrophages that were isolated from colon differs considerably from those isolated from the duodenum, jejunum and ileum, suggesting that the instructions that macrophages receive from these regions are variable. This makes it clear that distinct commensal populations in different regions of the intestine give signals to these cells, influencing their profiles [86] . The role of gut microbiota in macrophage and DC development is not clear.…”
Section: Cx3cr1mentioning
confidence: 99%