Identification and characterization of rodent ABCA1 in isolated type II pneumocytes

被引:53
作者
Bortnick, AE
Favari, E
Tao, JQ
Francone, OL
Reilly, M
Zhang, YZ
Rothblat, GH
Bates, SR
机构
[1] Univ Penn, Sch Med, Inst Environm Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Med Ctr, Philadelphia, PA 19104 USA
[3] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[4] Univ Parma, Inst Pharmacol & Biol Sci, I-43100 Parma, Italy
[5] Pfizer Inc, Groton, CT 06340 USA
关键词
phospholipid; cholesterol; lung; reverse cholesterol transport; surfactant secretion;
D O I
10.1152/ajplung.00077.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
ATP-binding cassette transporter A1 (ABCA1) promotes transfer of cholesterol and phospholipid from cells to lipid-free serum apolipoproteins. ABCA1 mRNA and protein expression in primary cultures of rodent type II cells was sensitive to upregulation with 5 muM 9-cis-retinoic acid (9cRA) and 6.2 mu M 22-hydroxycholesterol (22-OH). The increase in ABCA1 protein levels was time dependent and was maximal after 16 h of exposure to 9cRA + 22-OH. Inducible ABCA1 was also found in transformed cell lines of lung origin: WI38/VA13, A549, and NIH-H441 cells. Stimulation of ABCA1 in rat type II cells by 9cRA + 22-OH resulted in a four- or fivefold enhancement of efflux of radioactive phospholipid or cholesterol, respectively, from the pneumocytes to apolipoprotein AI (apo AI), whereas cAMP (0.3 mM) had no effect. ABCA1-mediated lipid efflux to apo AI was independent of the surfactant secretion pathway, inasmuch as upregulation of ABCA1 resulted in a reduction of secretagogue-stimulated surfactant phospholipid release. These studies demonstrate the presence of functional ABCA1 in type II cells from the lung.
引用
收藏
页码:L869 / L878
页数:10
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