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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chelvam, Venkatesh | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:33:04Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:33:04Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Shen, J., Chelvam, V., Cresswell, G., & Low, P. S. (2013). Use of folate-conjugated imaging agents to target alternatively activated macrophages in a murine model of asthma. Molecular Pharmaceutics, 10(5), 1918-1927. doi:10.1021/mp3006962 | en_US |
dc.identifier.issn | 1543-8384 | - |
dc.identifier.other | EID(2-s2.0-84877274683) | - |
dc.identifier.uri | https://doi.org/10.1021/mp3006962 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9438 | - |
dc.description.abstract | Pro-inflammatory macrophages play a prominent role in such autoimmune diseases as rheumatoid arthritis, Crohn's disease, psoriasis, sarcoidosis, and atherosclerosis. Because pro-inflammatory macrophages have also been shown to overexpress a receptor for the vitamin folic acid (i.e., folate receptor beta; FR-β), folate-linked drugs have been explored for use in imaging and treatment of these same diseases. To determine whether allergic inflammatory disorders might be similarly targeted with folate-linked drugs, we have examined the characteristics of macrophages that are prominent in the pathogenesis of asthma. We report here that macrophages from the lungs of mice with experimental allergic asthma express FR-β. We further document that these FR-β+ macrophages coexpress markers of alternatively activated (M2-type) macrophages, including the mannose receptor and arginase-1. Finally, we demonstrate that folate-conjugated fluorescent dyes and radioimaging agents can be specifically targeted to these asthmatic lung macrophages, with little uptake by macrophages present in healthy lung tissue. These data suggest strategies for the development of novel diagnostic agents for the imaging of asthma and other diseases involving alternatively activated macrophages. © 2013 American Chemical Society. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.source | Molecular Pharmaceutics | en_US |
dc.subject | arginase 1 | en_US |
dc.subject | ec 20 | en_US |
dc.subject | etarfolatide tc 99m | en_US |
dc.subject | fluorescent dye | en_US |
dc.subject | folate receptor 2 | en_US |
dc.subject | folic acid | en_US |
dc.subject | mannose receptor | en_US |
dc.subject | radiopharmaceutical agent | en_US |
dc.subject | technetium 99m | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | Arg1 protein, mouse | en_US |
dc.subject | arginase | en_US |
dc.subject | cell surface receptor | en_US |
dc.subject | EC20 folate peptide | en_US |
dc.subject | fluorescent dye | en_US |
dc.subject | folate receptor 2 | en_US |
dc.subject | folic acid | en_US |
dc.subject | lectin | en_US |
dc.subject | mannose binding lectin | en_US |
dc.subject | mannose receptor | en_US |
dc.subject | oligopeptide | en_US |
dc.subject | radiopharmaceutical agent | en_US |
dc.subject | technetium | en_US |
dc.subject | allergic asthma | en_US |
dc.subject | animal cell | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | animal tissue | en_US |
dc.subject | antiinflammatory activity | en_US |
dc.subject | article | en_US |
dc.subject | controlled study | en_US |
dc.subject | drug conjugation | en_US |
dc.subject | drug delivery system | en_US |
dc.subject | drug formulation | en_US |
dc.subject | drug targeting | en_US |
dc.subject | female | en_US |
dc.subject | lung alveolus macrophage | en_US |
dc.subject | lung parenchyma | en_US |
dc.subject | macrophage activation | en_US |
dc.subject | mouse | en_US |
dc.subject | nonhuman | en_US |
dc.subject | pathogenesis | en_US |
dc.subject | priority journal | en_US |
dc.subject | protein expression | en_US |
dc.subject | protein function | en_US |
dc.subject | radiography | en_US |
dc.subject | analogs and derivatives | en_US |
dc.subject | animal | en_US |
dc.subject | asthma | en_US |
dc.subject | Bagg albino mouse | en_US |
dc.subject | diagnostic imaging | en_US |
dc.subject | diagnostic use | en_US |
dc.subject | disease model | en_US |
dc.subject | human | en_US |
dc.subject | immunology | en_US |
dc.subject | lung | en_US |
dc.subject | macrophage | en_US |
dc.subject | metabolism | en_US |
dc.subject | procedures | en_US |
dc.subject | scintiscanning | en_US |
dc.subject | Animals | en_US |
dc.subject | Arginase | en_US |
dc.subject | Asthma | en_US |
dc.subject | Diagnostic Imaging | en_US |
dc.subject | Disease Models, Animal | en_US |
dc.subject | Female | en_US |
dc.subject | Fluorescent Dyes | en_US |
dc.subject | Folate Receptor 2 | en_US |
dc.subject | Folic Acid | en_US |
dc.subject | Humans | en_US |
dc.subject | Lectins, C-Type | en_US |
dc.subject | Lung | en_US |
dc.subject | Macrophage Activation | en_US |
dc.subject | Macrophages | en_US |
dc.subject | Mannose-Binding Lectins | en_US |
dc.subject | Mice | en_US |
dc.subject | Mice, Inbred BALB C | en_US |
dc.subject | Oligopeptides | en_US |
dc.subject | Radiopharmaceuticals | en_US |
dc.subject | Receptors, Cell Surface | en_US |
dc.subject | Technetium | en_US |
dc.title | Use of folate-conjugated imaging agents to target alternatively activated macrophages in a murine model of asthma | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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