EXPRESSION OF TRANSFORMING GROWTH FACTORS-ALPHA AND BETA(1) MESSENGER-RNA AND PRODUCT BY EOSINOPHILS IN NASAL POLYPS

被引:123
作者
ELOVIC, A
WONG, DTW
WELLER, PF
MATOSSIAN, K
GALLI, SJ
机构
[1] HARVARD UNIV,SCH DENT MED,DEPT ORAL MED & DIAGNOST SCI,DIV ORAL PATHOL,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA
[3] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
[4] BETH ISRAEL HOSP,BOSTON,MA
关键词
NASAL POLYPS; EOSINOPHILS; TGF-ALPHA; TGF-BETA(1); MESSENGER-RNA; CYTOKINES;
D O I
10.1016/0091-6749(94)90379-4
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Nasal polyps are thought to develop as a manifestation of a chronic inflammatory process involving the upper airways. The eosinophil characteristically represents a prominent component of the inflammatory cell infiltrate of these lesions. However, the major clinical problem associated with nasal polyps, nasal obstruction, reflects the proliferation of die stromal and epithelial elements, which constitute the bulk of these lesions. We recently reported that blood eosinophils of patients with hypereosinophilia can produce the cytokines transforming growth factors-alpha (TGF-alpha) and beta(1) (TGF-beta(1)). These cytokines have many biologic activities, which include the regulation of epithelial proliferation, the promotion of extracellular matrix formation, and the induction of angiogenesis. We therefore used in situ hybridization to determine whether the eosinophils that infiltrate nasal polyps express TGF-alpha and/or TGF-beta(1) messenger RNA and used immunohistochemistry to determine whether these eosinophils also express TGF-alpha and TGF-beta(1) proteins. We found that eosinophils represented a major source of both transforming growth factors in each case of nasal polyposis examined and that in most cases the majority of all eosinophils expressed both TGF-alpha and TGF-beta(1). These results suggest that production of TGF-alpha and TGF-beta(1) by the infiltrating eosinophils may contribute to some of the pathologic changes observed in nasal polyposis, such as thickening of the epithelial basement membrane, stromal fibrosis, angiogenesis, and epithelial and glandular hyperplasia.
引用
收藏
页码:864 / 869
页数:6
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