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J Comp Neurol


Title:"Neuronal expression of Cd36, Cd44, and Cd83 antigen transcripts maps to distinct and specific murine brain circuits"
Author(s):Glezer I; Bittencourt JC; Rivest S;
Address:"Department of Anatomy and Physiology, Laval University, Quebec, Canada G1V 4G2. iglezer@usp.br"
Journal Title:J Comp Neurol
Year:2009
Volume:517
Issue:6
Page Number:906 - 924
DOI: 10.1002/cne.22185
ISSN/ISBN:1096-9861 (Electronic) 0021-9967 (Linking)
Abstract:"Cells recruited by the innate immune response rely on surface-expressed molecules in order to receive signals from the local environment and to perform phagocytosis, cell adhesion, and others processes linked to host defense. Hundreds of surface antigens designated through a cluster of differentiation (CD) number have been used to identify particular populations of leukocytes. Surprisingly, we verified that the genes that encode Cd36 and Cd83 are constitutively expressed in specific neuronal cells. For instance, Cd36 mRNA is expressed in some regions related to circuitry involved in pheromone responses and reproductive behavior. Cd44 expression, reanalyzed and detailed here, is associated with the laminar formation and midline thalamic nuclei in addition to striatum, extended amygdala, and a few hypothalamic, cortical, and hippocampal regions. A systemic immune challenge was able to increase Cd44 expression quickly in the area postrema and motor nucleus of the vagus but not in regions presenting expressive constitutive expression. In contrast to Cd36 and Cd44, Cd83 message was widely distributed from the olfactory bulb to the brain stem reticular formation, sparing the striatopallidum, olivary region, and cerebellum. Its pattern of expression nevertheless remained strongly associated with hypothalamic, thalamic, and hindbrain nuclei. Unlike the other transcripts, Cd83 mRNA was rapidly modulated by restraint stress. Our results indicate that these molecules might play a role in specific neural circuits and present functions other than those attributed to leukocyte biology. The data also suggest that these surface proteins, or their associated mRNA, could be used to label neurons in specific circuits/regions"
Keywords:"Animals Antigens, CD/*metabolism Brain/*physiology CD36 Antigens/*metabolism Hyaluronan Receptors/*metabolism Immunoglobulins/*metabolism Inflammation/chemically induced/metabolism Lipopolysaccharides/toxicity Male Membrane Glycoproteins/*metabolism Mice;"
Notes:"MedlineGlezer, Isaias Bittencourt, Jackson C Rivest, Serge eng FRN12594/Canadian Institutes of Health Research/Canada Research Support, Non-U.S. Gov't 2009/10/22 J Comp Neurol. 2009 Dec 20; 517(6):906-24. doi: 10.1002/cne.22185"

 
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