Regular immunohistochemical localization of endothelin-1 and endothelin-B receptor in normal, hyperplastic and neoplastic human adrenocortical cells

被引:25
作者
Hiraki, H
Hoshi, N
Hasegawa, H
Tanigawa, T
Emura, I
Seito, T
Yamaki, T
Fukuda, T
Watanabe, K
Suzuki, T
机构
[1] FUKUSHIMA MED COLL,DEPT PATHOL,FUKUSHIMA 96012,JAPAN
[2] NIIGATA UNIV,SCH MED,DEPT SURG PATHOL,NIIGATA,JAPAN
[3] IMMUNOBIOL LABS,GUNMA,JAPAN
[4] NIIGATA UNIV,SCH MED,DEPT SURG PATHOL,NIIGATA,JAPAN
关键词
adrenocortical cells; endothelin; endothelin receptor; immunohistochemistry;
D O I
10.1111/j.1440-1827.1997.tb03730.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The localization of endothelin (ET)-1/big ET-1, ET-3/big ET-3, ET-A and ET-B receptor was immunohistochemically examined in human adrenal glands composed of 36 normal cases, nine hyperplasia, 70 adenomas and seven carcinomas of cortical cells. In normal adrenals, ET-1/big ET-1 and ET-B receptor were regularly detected in the cortical cells, especially in the zona fasciculata for ET-1 and zona glomerulosa for ET-B receptor but not in the medulla, while ET-A receptor localized occasionally in endothelial cells or rarely in cortical cells and ET-3/big ET-3 was very limited in the cortical cells. In hyperplasia, adenoma and carcinoma, ET-1/big ET-1 and ET-B receptor showed frequent localization, although focal distribution of the ET-B receptor was rather predominant in these groups. ET-A receptor and ET-3/big ET-3 were very infrequently expressed. Functioning versus non-functioning and hypertensive versus normotensive cases revealed no significant differences in the frequency of positive cells for ET-1/big ET-1, ET-3/big ET-3, ET-A receptor or ET-B receptor. Alternatively, the frequency of immunoreactivity to ET-1/big ET-1 or ET-B receptor significantly decreased in hyperplasia, adenoma and carcinoma, when compared with that of normal adrenal cortex. The present study, therefore, indicates that ET-1/big ET-1 and ET-B receptor are a prevalent ligand-receptor system in normal and hyperplastic/neoplastic adrenocortical cells, even with a malignant profile, and may contribute in maintaining adrenocortical cell function or cell viability but not cell growth or systemic hypertension.
引用
收藏
页码:117 / 125
页数:9
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