Higher expression of BDNF receptor gp145trkB is associated with lower apoptosis intensity in T cell lines in multiple sclerosis

被引:23
作者
De Santi, Lorenzo [1 ]
Cantalupo, Loredana [1 ]
Tassi, Maristella [2 ]
Raspadori, Donatella [2 ]
Cioni, Chiara [1 ]
Annunziata, Pasquale [1 ]
机构
[1] Univ Siena, Dept Neurol & Behav Sci, I-53100 Siena, Italy
[2] Univ Siena, Hematol & Transplants Unit, I-53100 Siena, Italy
关键词
Apoptosis; Brain-derived neurotrophic factor; gp145trkB; Multiple sclerosis; Neurotrophins; T cells; NEUROTROPHIC FACTOR; GLATIRAMER ACETATE; PERIPHERAL-BLOOD; NERVOUS-SYSTEM; BRAIN-LESIONS; IMMUNE-SYSTEM; IN-VITRO; B-CELLS; TRKB; PRODUCE;
D O I
10.1016/j.jns.2008.10.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
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-Tcell 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. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:65 / 70
页数:6
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