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- Title
Spinal cord injury induces expression of RGS7 in microglia/macrophages in rats.
- Authors
Hausmann, Oliver N.; Hu, Wen‐Hui; Keren‐Raifman, Tal; Witherow, D. Scott; Wang, Qiang; Levay, Konstantin; Frydel, Beata; Z. Slepak, Vladlen; R. Bethea, John
- Abstract
Abstract RGS proteins regulate G protein-mediated signalling pathways through direct interaction with the Gα subunits and facilitation of GTP hydrolysis. An RGS subfamily consisting of RGS 6, 7, 9, and 11 also interacts with the G protein β subunit Gβ5 via a characteristic Gγ-like domain. Thus far, these complexes were found only in neurons, with RGS7 being the most widely distributed in the brain. Here we confirm the expression of RGS7 in spinal neurons and show as a novel finding that following an experimental spinal cord injury in rats, expression of RGS7 is induced in a subpopulation of other cells. Immunofluorescent confocal microscopy using a series of cell specific antibodies identified these RGS7 positive cells as activated microglia and/or invading peripheral macrophages. To rule out interference from the adjacent neurons and confirm the presence of RGS7-Gβ5 complex in inflammatory cells, we performed immunocytochemistry, RT-PCR, Western blot, and immunoprecipitation using microglial (BV2) and peripheral macrophage (RAW) cell lines. Expression of RGS7 mRNA and protein are nearly undetectable in non-stimulated BV2 and RAW cells, but remarkably increased after stimulation with LPS or TNF-α In addition, RGS7-positive cells were also found in the perinodular rim in the rat spleen. Our findings show that RGS7-Gβ5 complex is expressed in immunocompetent cells such as resident microglia and peripheral macrophages following spinal cord injury. This expression might contribute to the post-traumatic inflammatory responses in the central nervous system.
- Subjects
SPINAL cord injuries; MICROGLIA; MACROPHAGES; PROTEINS
- Publication
European Journal of Neuroscience, 2002, Vol 15, Issue 4, p602
- ISSN
0953-816X
- Publication type
Article
- DOI
10.1046/j.1460-9568.2002.01916.x