1999
DOI: 10.1053/gast.1999.0029900359
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Chemokine receptor expression by human intestinal epithelial cells

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Cited by 203 publications
(174 citation statements)
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References 62 publications
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“…4h), but not on the enterocytes of adjacent villi. The two chemokine receptors, how- ever, were expressed in the crypts of the small intestine, as already reported in the colon (21).…”
Section: X4 and Galcer-specific Antibodies Prevent Infection Of Caco2supporting
confidence: 74%
See 1 more Smart Citation
“…4h), but not on the enterocytes of adjacent villi. The two chemokine receptors, how- ever, were expressed in the crypts of the small intestine, as already reported in the colon (21).…”
Section: X4 and Galcer-specific Antibodies Prevent Infection Of Caco2supporting
confidence: 74%
“…Initial infection with HIV-1 is usually transmitted with R5 viruses (20). Several epithelial cell lines and intestinal crypts and villi express various chemokine receptors including CXCR4 and CCR5 (21).…”
mentioning
confidence: 99%
“…14,15 Colonic epithelium shows upregulation of RANTES (regulated upon activation normal T-cell expressed and secreted), which is the natural ligand for the chemokine receptor CCR5. 16 During episodes of intestinal inflammation, CCR5 is upregulated on activated Th1-type intestinal lamina propria and intraepithelial lymphocytes as well as dendritic cells, supporting a role for this chemokine in lymphocyte recruitment to the gut. 17 CCR5 may also play a role in lymphocyte recruitment and immune responses within the liver.…”
Section: Introductionmentioning
confidence: 94%
“…CCR5 has been shown to be abundantly expressed in colon epithelial cell lines and regulate proinflammatory chemokine production. 32 A naturally occurring variant of CCR5 exists, where a 32-bp deletion results in synthesis of a non-functional receptor due to generation of a premature stop codon. This D32 variant was first identified in individuals resistant to HIV-1 infection, and was subsequently associated with reduced risk of asthma, 22 possibly pointing to less liability to chronic inflammation.…”
Section: European Journal Of Human Geneticsmentioning
confidence: 99%