INT157466
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Furthermore, fractalkine and CX3CR1 mRNA overexpressions were associated with enhanced lymphocyte and macrophage infiltration. | |||||||||||||||
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CX3CR1, but not fractalkine, mRNA was overexpressed in CP. | |||||||||||||||
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In contrast, the protein levels of both CX3CR1 and fractalkine were upregulated. | |||||||||||||||
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It interacts with the unique receptor CX3CR1 that is expressed on monocytes, natural killer cells, and some T cells. | |||||||||||||||
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Soluble fractalkine/CX3CL1 is a potent chemoattractant for CX3CR1+ leukocytes. | |||||||||||||||
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Individual cell populations in PB, BKmig and BKnon were identified according to their surface expression levels of CD34 (Miltenyi), KDR (R&D systems), CXCR4 (BD), CD14 (Miltenyi), CD16 (BD), CX3CR1 (Caltag) by flow cytometry (Fig. | |||||||||||||||
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Individual cell populations in PB, BKmig and BKnon were identified according to their surface expression levels of CD34 (Miltenyi), KDR (R&D systems), CXCR4 (BD), CD14 (Miltenyi), CD16 (BD), CX3CR1 (Caltag) by flow cytometry (Fig. | |||||||||||||||
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No significant differences in co-expression of CX3CR1, CXCR4, or KDR were detected by comparing H vs. | |||||||||||||||
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The fractalkine receptor CX3CR1, previously associated with recruitment of pro-atherosclerotic cells and their retention in the vessel wall [15], was co-expressed on the majority of CD16pos monocyte subtypes and less frequent on CD14hiCD16neg monocytes, with no significant differences between H and T1D (Fig. 1B). | |||||||||||||||
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Most CXC and CC chemokine receptors mentioned above as well as XCR1 and CX3CR1 are expressed in the arthritic synovium [14,17,18].
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Upregulated fractalkine and CX3CR1 levels were present in the early stage of diabetic kidney disease in rats.28 The aforementioned data suggest that fractalkine and CX3CR1 have an important role in the progression of diabetic nephropathy, functioning as an arrest chemokine in monocyte/macrophage adhesion before migration into the kidney. | |||||||||||||||
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In this way, membrane-bound fractalkine contributes to the adhesion of CX3CR1-expressing leukocytes. | |||||||||||||||
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Furthermore, fractalkine and CX3CR1 mRNA overexpressions were associated with enhanced lymphocyte and macrophage infiltration. | |||||||||||||||
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These were CCR1, CCR2a, CCR5, CCR7, CCR9, CX3CR1, CXCR1, CXCR2, CXCR4, CXCR5, CXCR6 (STRL33) and Bob (Table 3). | |||||||||||||||
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Fractalkine levels have only been rarely determined in patients; however, it has been shown that Alzheimer patients express enhanced fractalkine levels, correlating with the Mini-Mental State Examination (MMSE) score.20 Another study also reported that fractalkine levels are enhanced in WegenerÂ’s granulomatosis.21 In patients with coronary artery disease fractalkine plasma levels were enhanced and then reduced after statin therapy.22 When CX3CR1 genotypes were analyzed in patients with acute coronary syndromes and healthy controls, CX3CR1-I249 heterozygosity was associated with a markedly reduced risk of acute coronary events, independent of established coronary risk factors such as smoking or diabetes.23,24 | |||||||||||||||
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Fractalkine levels have only been rarely determined in patients; however, it has been shown that Alzheimer patients express enhanced fractalkine levels, correlating with the Mini-Mental State Examination (MMSE) score.20 Another study also reported that fractalkine levels are enhanced in WegenerÂ’s granulomatosis.21 In patients with coronary artery disease fractalkine plasma levels were enhanced and then reduced after statin therapy.22 When CX3CR1 genotypes were analyzed in patients with acute coronary syndromes and healthy controls, CX3CR1-I249 heterozygosity was associated with a markedly reduced risk of acute coronary events, independent of established coronary risk factors such as smoking or diabetes.23,24 | |||||||||||||||
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express only select types of the numerous chemokine receptors (for example, CCR1, 2, 5, 7, and 8 as well as CX3CR1), representing a partially specific basis for prominent trafficking of monocyte/M? | |||||||||||||||
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It interacts with the unique receptor CX3CR1 that is expressed on monocytes, natural killer cells, and some T cells. | |||||||||||||||
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