INT176892
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
When necessary, for example, in case of degenerative MR or ruptured chordae tendineae with wide prolapse, a second clip can be implanted (Figure 3). | |||||||||||||||
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All the hazards associated with diagnostic MR also apply to interventional procedures. | |||||||||||||||
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MR is a common finding in heart failure patients. | |||||||||||||||
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The specificity of MR CRD47-Fc binding to DV sE was further examined by blot overlay. | |||||||||||||||
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Terminal fucose is a reported ligand of MR and as such is the likely ligand on this source of DV antigen. | |||||||||||||||
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To further evaluate MR as a potential DV receptor, we examined binding of DV to human MR-transfected 3T3 cells (3T3.hMR). | |||||||||||||||
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We showed that MR can bind in ELISA to Japanese encephalitis virus and tick-borne encephalitis virus, both of which are reported to have glycosylated envelope proteins. | |||||||||||||||
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This, combined with the observation that MDDC express both DC-SIGN and MR [22], and our demonstration that the presence of MR alone is sufficient to confer DV binding to transfected cells, suggest that glycosylation at Asn-67 may be relevant for mediating MR binding, in addition to that of DC-SIGN. | |||||||||||||||
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Given the interaction of DV with MR described above, it was important to characterise the glycans on the human cellproduced sE, especially since we are unaware of any similar analysis in the literature. | |||||||||||||||
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We expanded our study of the interaction of MR with DV by demonstrating binding of CRD4-7-Fc to all four serotypes of DV. | |||||||||||||||
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These receptors recognize major histocompatibility complex class I (MHC-I) antigens, which inhibit cytotoxicity against MHC-I-expressing target cells. | |||||||||||||||
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In this study we show that MR binds to DV grown in mosquito cells and to recombinant mammalian cellproduced DV envelope glycoprotein. | |||||||||||||||
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To our knowledge, we show for the first time that the MØ mannose receptor (MR) binds to all four serotypes of DV and specifically to the envelope glycoprotein. | |||||||||||||||
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ELISA data showed that both CRD47-Fc and MR-HA both bound to Japanese encephalitis virus (inactivated vaccine antigen) and tick-borne encephalitis virus (inactivated, mouse brain-grown) (data not shown). | |||||||||||||||
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Glycan analysis, ELISA, and blot overlay assays demonstrate that MR binds via its carbohydrate recognition domains to mosquito and human cellproduced DV antigen. | |||||||||||||||
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Detection of MR fusion protein binding to DV antigen ELISA. | |||||||||||||||
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Fig. 12A patient with myeloma after bone marrow transplantation: The bone marrow of the lumbar spine shows a diffuse hypointense signal intensity on both plain T1-weighted (left) and fat-saturated T2-weighted (right) MR images | |||||||||||||||
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After the conditioning therapy for allogenic marrow transplantation, the patients reach complete aplasia, are usually isolated on a bone marrow transplantation unit and should only undergo MR imaging for vital indications. | |||||||||||||||
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Additional patients with hematologic malignancies may undergo MR imaging for evaluations of other pathologies, outside the bone marrow. | |||||||||||||||
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A recombinant MR fusion protein (CRD47-Fc) was shown to recognize DV envelope (E) protein in ELISA and blot overlays, and binding was inhibited by mannose, fucose and EDTA. | |||||||||||||||
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