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CD4 microglial expression correlates with spontaneous clinical improvement in the acute Lewis rat EAE model.
MedLine Citation:
PMID:  19246105     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
CD4 is a molecule commonly expressed on the surface of T-helper lymphocytes with a recognized critical role in the antigen presentation process that has also been reported in monocytes and macrophages, although its role in these cells remains unknown. The objective of the present study was to analyze whether experimental conditions involving a potent acquired immune component, as occurs in experimental autoimmune encephalomyelitis (EAE), are able to induce CD4 expression in the population of microglia/macrophages. Myelin Basic Protein (MBP) immunized female Lewis rats, were examined at different phases during the course of EAE according to their clinical score. Spinal cords were analyzed by flow cytometry for CD11b, CD4 and CD45, by histochemistry for NDPase and by immunohistochemistry for ED2, Iba1, CD45 and CD4. Flow cytometry analysis showed that EAE induced CD4 expression in macrophages (CD11b+/CD45(high)) and microglia (in both CD11b+/CD45(intermediate) and CD11b+/CD45(low) phenotypes). Noticeably, microglial CD4 expression was found during the recovery phase and was maintained until 40 days post-induction. In agreement, immunolabelled sections revealed CD4 expression in microglial cells with ramified morphology during the recovery and post-recovery phases. In conclusion, our results indicate that, in this EAE model, perivascular cells, microglia and macrophages showed different dynamics during the course of the disease in close relation with symptomatology and that microglial cells expressed CD4 interestingly during the recovery phase, suggesting a role of microglial CD4 expression in the resolution of the immune response.
Authors:
Beatriz Almolda; Manuela Costa; Maria Montoya; Berta González; Bernardo Castellano
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-02-26
Journal Detail:
Title:  Journal of neuroimmunology     Volume:  209     ISSN:  1872-8421     ISO Abbreviation:  J. Neuroimmunol.     Publication Date:  2009 Apr 
Date Detail:
Created Date:  2009-04-21     Completed Date:  2009-06-22     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8109498     Medline TA:  J Neuroimmunol     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  65-80     Citation Subset:  IM    
Affiliation:
Unit of Histology, Department of Cell Biology, Physiology and Immunology, Institute of Neuroscience, Faculty of Medicine, Universitat Autònoma de Barcelona, Bellaterra, Spain. beatriz.almolda@uab.es
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MeSH Terms
Descriptor/Qualifier:
Acute Disease
Animals
Antigens, CD11 / analysis,  metabolism
Antigens, CD4 / metabolism*
Antigens, CD45 / analysis,  metabolism
Antigens, Surface / analysis,  metabolism
Central Nervous System / immunology*,  metabolism,  physiopathology
Chemotaxis, Leukocyte / immunology
Disease Models, Animal
Encephalomyelitis, Autoimmune, Experimental / immunology*,  physiopathology
Female
Flow Cytometry
Gliosis / immunology,  physiopathology
Immunity, Innate / immunology
Macrophages / immunology
Microglia / immunology*
Rats
Rats, Inbred Lew
Recovery of Function / immunology*
Spinal Cord / immunology,  metabolism,  physiopathology
Chemical
Reg. No./Substance:
0/Antigens, CD11; 0/Antigens, CD4; 0/Antigens, Surface; EC 3.1.3.48/Antigens, CD45

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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