Bortnick Anna E, Favari Elda, Tao Jian-Qin, Francone Omar L, Reilly Muredach, Zhang Yuzhen, Rothblat George H, Bates Sandra R
Institute for Environmental Medicine, University of Pennsylvania, 1 John Morgan Bldg., 36th and Hamilton Walk, Philadelphia, PA 19104-6068, USA.
Am J Physiol Lung Cell Mol Physiol. 2003 Oct;285(4):L869-78. doi: 10.1152/ajplung.00077.2003. Epub 2003 Aug 8.
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 microM 9-cis-retinoic acid (9cRA) and 6.2 microM 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.
ATP结合盒转运蛋白A1(ABCA1)促进胆固醇和磷脂从细胞向无脂血清载脂蛋白的转运。在啮齿动物II型细胞的原代培养物中,ABCA1 mRNA和蛋白表达对5微摩尔9-顺式视黄酸(9cRA)和6.2微摩尔22-羟基胆固醇(22-OH)的上调敏感。ABCA1蛋白水平的增加是时间依赖性的,在暴露于9cRA + 22-OH 16小时后达到最大值。在源自肺的转化细胞系中也发现了可诱导的ABCA1:WI38/VA13、A549和NIH-H441细胞。9cRA + 22-OH刺激大鼠II型细胞中的ABCA1,导致放射性磷脂或胆固醇分别从肺细胞向载脂蛋白AI(apo AI)的流出增强四倍或五倍,而环磷酸腺苷(0.3毫摩尔)则无作用。ABCA1介导的脂质向apo AI的流出独立于表面活性剂分泌途径,因为ABCA1的上调导致促分泌剂刺激的表面活性剂磷脂释放减少。这些研究证明了肺II型细胞中存在功能性ABCA1。