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Higher expression of BDNF receptor gp145trkB is associated with lower apoptosis intensity in T cell lines in multiple sclerosis.
- Source :
-
Journal of the neurological sciences [J Neurol Sci] 2009 Feb 15; Vol. 277 (1-2), pp. 65-70. Date of Electronic Publication: 2008 Nov 06. - Publication Year :
- 2009
-
Abstract
- Conflicting data exist on expression of gp145trkB, the high affinity receptor for brain-derived neurotrophic factor (BDNF), on peripheral blood immunocompetent cells in multiple sclerosis (MS). We analyzed expression of gp145trkB by western blotting and flow cytometry in myelin basic protein (MBP)- and ovalbumin (OVA)-T cell lines prepared from 12 patients with relapsing-remitting MS and 12 normal healthy subjects (NHS) and correlated it with activation-induced apoptosis. We found a higher percentage of gp145trkB-expressing MBP-T cells in MS patients than in NHS (p=0.011). gp145trkB was mainly expressed by CD8(+) T cells to a higher extent in MS patients than in NHS (p=0.04). MBP-T cell lines from MS patients showed significantly lower apoptosis intensity than those from NHS (p=0.011). We found also a significant negative correlation between gp145trkB expression and apoptosis intensity in MS patients only (p=0.02). OVA-T cell lines showed a gp145trkB expression similar to that of MBP-T cell lines, with a higher expression in MS patients than NHS, and similar correlations with apoptosis intensity in MS. These findings suggest that gp145trkB is mainly expressed on T cell lines from MS patients and that the BDNF/gp145trkB axis is involved in the regulation of peripheral T cell apoptosis in MS.
- Subjects :
- Adult
Blotting, Western
Brain-Derived Neurotrophic Factor metabolism
Cell Line
Cell Survival immunology
Female
Flow Cytometry
Humans
Male
T-Lymphocytes metabolism
Apoptosis immunology
Multiple Sclerosis genetics
Multiple Sclerosis immunology
Receptor, trkB genetics
T-Lymphocytes cytology
T-Lymphocytes physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0022-510X
- Volume :
- 277
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Journal of the neurological sciences
- Publication Type :
- Academic Journal
- Accession number :
- 18992902
- Full Text :
- https://doi.org/10.1016/j.jns.2008.10.006