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Developmental and glucocorticoid regulation of surfactant protein mRNAs in preterm lambs
被引:57
作者:
Tan, RC
Ikegami, M
Jobe, AH
Yao, LY
Possmayer, F
Ballard, PL
机构:
[1] Univ Penn, Sch Med, Childrens Hosp Philadelphia, Dept Pediat,Abramson Res Ctr 416, Philadelphia, PA 19104 USA
[2] Childrens Hosp, Med Ctr, Cincinnati, OH 45229 USA
[3] Univ Western Ontario, St Josephs Hlth Ctr, Lawson Res Inst, Dept Obstet & Gynecol & Biochem, London, ON N6A 4V2, Canada
[4] Univ Western Ontario, London Hlth Sci Ctr, London, ON N6A 4V2, Canada
关键词:
betamethasone;
ontogeny;
D O I:
10.1152/ajplung.1999.277.6.L1142
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
Glucocorticoid treatment increases content of surfactant protein (SP) A and SP-B in lung tissue and lavage fluid of preterm lambs. To investigate this process, we determined the ontogeny and glucocorticoid induction of SP mRNAs. In separate treatment protocols, each with its own controls, sheep were injected with betamethasone 15 h, 48 h or weekly for 1-4 doses before preterm delivery. Using ovine SP cDNAs, we found an increase equal to or more than threefold in basal levels of all three SP mRNAs between 125 days and term. After betamethasone treatment, SP-B and SP-C mRNA levels increased by 15 h and all SP mRNAs were elevated after 24 h (greater than or equal to 2-fold); mRNA levels in fetuses delivered 1-3 wk after betamethasone were not different from control. me conclude that in vivo betamethasone rapidly induces a coordinated increase in SP mRNAs, which is fully reversible within 7 days despite repetitive doses of betamethasone. Similar increases in mRNA and protein contents for SP-A and SP-B suggest that glucocorticoid regulation of these SPs in vivo is primarily pretranslational.
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页码:L1142 / L1148
页数:7
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