EXPRESSION OF TRANSFORMING GROWTH FACTOR-ALPHA IN MIDGESTATION HUMAN FETAL LUNG

被引:27
|
作者
STRANDJORD, TP
CLARK, JG
HODSON, WA
SCHMIDT, RA
MADTES, DK
机构
[1] UNIV WASHINGTON,DEPT MED,DIV PULM & CRIT CARE MED,SEATTLE,WA 98195
[2] UNIV WASHINGTON,DEPT PATHOL,SEATTLE,WA 98195
[3] FRED HUTCHINSON CANC RES CTR,SEATTLE,WA 98104
关键词
D O I
10.1165/ajrcmb/8.3.266
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming growth factor-alpha (TGF-alpha), a member of the epidermal growth factor (EGF) family, is a potent mitogen for several cell types. To investigate the possible role of TGF-alpha in the development of mid-gestation human fetal lung, we studied its distribution with immunohistochemistry and determined levels of steady-state TGF-alpha mRNA by Northern analysis of cellular RNA isolates from lung. Lung was obtained from fetuses at 10 to 22 wk of gestation (n = 14) and immunostained for TGF-alpha. TGF-alpha was localized in epithelial cells at all gestational ages examined. Immunostaining was particularly prominent in bronchiolar epithelial cells. TGF-alpha immunoreactivity was also associated with arterial smooth muscle cells, as well as with nerves. Occasional chondrocytes were also associated with TGF-alpha immunoreactivity. Total cellular RNA was isolated from lung tissue obtained from additional fetuses at gestational ages 10 to 24 wk (n = 22). TGF-alpha mRNA was present in RNA extracts of all fetal lungs studied. We conclude that TGF-alpha is probably produced in human fetal lung during mid-gestation. The prominent immunostaining of bronchiolar epithelial cells for TGF-alpha is consistent with its playing a role in distal airway formation.
引用
收藏
页码:266 / 272
页数:7
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