Immunohistochemical analysis of Bcl-2, Bax and Bak expression in thyroid glands from patients with Graves' disease

被引:12
作者
Hiromatsu, Y
Kaku, H
Mukai, T
Miyake, T
Fukutani, T
Koga, M
Shoji, S
Toda, S
Koike, N
机构
[1] Kurume Univ, Sch Med, Dept Med, Div Endocrinol & Metab, Kurume, Fukuoka 8300011, Japan
[2] Saga Univ, Fac Med, Dept Pathol & Biodef, Div Cellular & Mol Pathol, Saga 8498501, Japan
[3] Koike Hosp, Saga 8400862, Japan
关键词
apoptosis; Bcl-2; Bax; Bak; Graves' disease; n;
D O I
10.1507/endocrj.51.399
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
In order to clarify the role of apoptosis and the expression of Bcl-2 family proteins in the pathology of Graves' disease (GD), we evaluated the apoptosis by in situ end-labeling of fragmented DNA and the expression of Bcl-2, Bax and Bak by immunohistochemistry in thyroid tissues from 20 patients with GD and in normal thyroid tissues from 6 patients with follicular adenoma (N). Apoptotic nuclei were found in thyrocytes and in germinal center of lymphoid follicles. Bcl-2 was strongly expressed in both GD and N thyrocytes. Bax was not expressed in either GD or N thyrocytes. Bak was expressed in thyrocytes From 5 of 20 patients with GD, while it was detected in all N thyrocytes. In lymphoid follicles Bcl-2 was expressed in the mantle zone, while Bax and Bak were both expressed in the germinal center. The percentage of apoptotic nuclei in GD thyrocytes was low (0similar to3.6%), and negatively correlated with the weight of the thyroid glands resected (rs = -0.43, P<0.05). It was greater in Bak-positive GD thyrocytes than in Bak-negative ones (mean +/- SD; 1.7 +/- 0.7% vs. 0.7 +/- 0.9%, P<0.05). These findings suggest that the differential expression of Bcl-2 family proteins in both thyrocytes and lymphoid follicles may be involved in the pathology of GD.
引用
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页码:399 / 405
页数:7
相关论文
共 33 条
[1]
Apoptosis and thyroiditis [J].
Arscott, PL ;
Baker, JR .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 87 (03) :207-217
[2]
Expression of bcl-2 and bax in regenerating rat renal tubules following ischemic injury [J].
Basile, DP ;
Liapis, H ;
Hammerman, MR .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1997, 272 (05) :F640-F647
[3]
Expression of the cell death-inducing gene bax in carcinomas developed from the follicular cells of the thyroid gland [J].
Branet, F ;
Brousset, P ;
Krajewski, S ;
Schlaifer, D ;
Selves, J ;
Reed, JC ;
Caron, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (07) :2726-2730
[4]
Apoptosis and autoimmune thyroid disease: following a TRAIL to thyroid destruction? [J].
Bretz, JD ;
Baker, JR .
CLINICAL ENDOCRINOLOGY, 2001, 55 (01) :1-11
[5]
Brocker M, 1996, EXP CLIN ENDOCR DIAB, V104, P20
[6]
Altered expression of bcl-2, bcl-X, bax, and c-fos colocalizes with DNA fragmentation and ischemic cell damage following middle cerebral artery occlusion in rats [J].
Gillardon, F ;
Lenz, C ;
Waschke, KF ;
Krajewski, S ;
Reed, JC ;
Zimmermann, M ;
Kuschinsky, W .
MOLECULAR BRAIN RESEARCH, 1996, 40 (02) :254-260
[7]
Differential regulation of Fas-mediated apoptosis in both thyrocyte and lymphocyte cellular compartments correlates with opposite phenotypic manifestations of autoimmune thyroid disease [J].
Giordano, C ;
Richiusa, P ;
Bagnasco, M ;
Pizzolanti, G ;
Di Blasi, F ;
Sbriglia, MS ;
Mattina, A ;
Pesce, G ;
Montagna, P ;
Capone, F ;
Misiano, G ;
Scorsone, A ;
Pugliese, A ;
Galluzzo, A .
THYROID, 2001, 11 (03) :233-244
[8]
Potential involvement of fas and its ligand in the pathogenesis of Hashimoto's thyroiditis [J].
Giordano, C ;
Stassi, G ;
DeMaria, R ;
Todaro, M ;
Richiusa, P ;
Papoff, G ;
Ruberti, G ;
Bagnasco, M ;
Testi, R ;
Galluzzo, A .
SCIENCE, 1997, 275 (5302) :960-963
[9]
Hammond LJ, 1997, J PATHOL, V182, P138, DOI 10.1002/(SICI)1096-9896(199706)182:2<138::AID-PATH810>3.0.CO
[10]
2-F