REGULATION OF SURFACTANT PROTEIN-D EXPRESSION BY GLUCOCORTICOIDS IN-VITRO AND IN-VIVO

被引:43
作者
DETERDING, RR
SHIMIZU, H
FISHER, JH
SHANNON, JM
机构
[1] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT MED,DENVER,CO 80206
[2] UNIV COLORADO,HLTH SCI CTR,DEPT MED,DIV PULM & CRIT CARE MED,DENVER,CO 80262
关键词
D O I
10.1165/ajrcmb.10.1.8292379
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
SP-D is a recently described lung-associated protein that is produced by alveolar type II cells and may function in pulmonary host defenses. Since little is known regarding the hormonal regulation of SP-D, and since the other surfactant proteins (SP-A, SP-B, and SP-C) am known to be regulated by glucocorticoids, we sought to determine the effects of glucocorticoids on SP-D mRNA and protein expression, both in vitro and in vivo, in the fetal rat lung. In vitro experiments were performed on lung explants from fetuses on gestational day 15 or 18. Explants were cultured in serum-free conditions with or without hydrocortisone for 3 days. SP-D mRNA expression was evaluated by Northern blot analysis. SP-D protein expression was analyzed using a polyclonal antibody against SP-D and standard immunohistochemical techniques. The expression of SP-D mRNA increased in fetal day 15 explants but remained unchanged in fetal day 18 explants cultured without the addition of hydrocortisone, compared with in vivo controls. The addition of hydrocortisone resulted in increases in SP-D mRNA expression at both gestational ages. This pattern of SP-D mRNA expression was compared with the expression of the other surfactant proteins and found to be most similar to that of SP-B. In vivo experiments were performed using maternal administration of dexamethasone (1 mg/kg) or an equal volume of saline on fetal days 15, 16, and 17 or on fetal day 17 with sacrifice on fetal day 18. Precocious expression of SP-D mRNA and protein was seen in vivo with maternal administration of dexamethasone. These findings demonstrate that SP-D is regulated by glucocorticoids both in vitro and in vivo and suggest that SP-D is differentially regulated from the other surfactant proteins.
引用
收藏
页码:30 / 37
页数:8
相关论文
共 50 条
[1]   REGULATION OF PULMONARY SURFACTANT APOPROTEIN SP 28-36 GENE IN FETAL HUMAN-LUNG [J].
BALLARD, PL ;
HAWGOOD, S ;
LILEY, H ;
WELLENSTEIN, G ;
GONZALES, LW ;
BENSON, B ;
CORDELL, B ;
WHITE, RT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9527-9531
[2]   HORMONAL-REGULATION OF PULMONARY SURFACTANT [J].
BALLARD, PL .
ENDOCRINE REVIEWS, 1989, 10 (02) :165-181
[3]   ROLE OF CALCIUM-IONS IN THE STRUCTURE AND FUNCTION OF PULMONARY SURFACTANT [J].
BENSON, BJ ;
WILLIAMS, MC ;
SUEISHI, K ;
GOERKE, J ;
SARGEANT, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 793 (01) :18-27
[4]   PULMONARY SURFACTANT PROTEIN-B (SP-B) - STRUCTURE-FUNCTION-RELATIONSHIPS [J].
COCHRANE, CG ;
REVAK, SD .
SCIENCE, 1991, 254 (5031) :566-568
[5]  
CROUCH E, 1991, AM J PATHOL, V139, P765
[6]   SURFACTANT PROTEIN-D - SUBCELLULAR-LOCALIZATION IN NONCILIATED BRONCHIOLAR EPITHELIAL-CELLS [J].
CROUCH, E ;
PARGHI, D ;
KUAN, SF ;
PERSSON, A .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :L60-L66
[7]   DEVELOPMENTAL EXPRESSION OF PULMONARY SURFACTANT PROTEIN-D (SP-D) [J].
CROUCH, E ;
RUST, K ;
MARIENCHEK, W ;
PARGHI, D ;
CHANG, D ;
PERSSON, A .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1991, 5 (01) :13-18
[8]  
CROUCH E, 1993, J BIOL CHEM, V268, P2976
[9]   PRIMARY TRANSLATION PRODUCTS OF PULMONARY SURFACTANT PROTEIN-D [J].
CROUCH, E ;
RUST, K ;
PERSSON, A ;
MARIENCHECK, W ;
MOXLEY, M ;
LONGMORE, W .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (04) :L247-L253
[10]   PULMONARY SURFACTANT AND ITS COMPONENTS INHIBIT SECRETION OF PHOSPHATIDYLCHOLINE FROM CULTURED RAT ALVEOLAR TYPE-II CELLS [J].
DOBBS, LG ;
WRIGHT, JR ;
HAWGOOD, S ;
GONZALEZ, R ;
VENSTROM, K ;
NELLENBOGEN, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (04) :1010-1014