Storey M K, Byers D M, Cook H W, Ridgway N D
Atlantic Research Centre, Dalhousie University, Halifax, Nova Scotia, Canada.
J Lipid Res. 1997 Apr;38(4):711-22.
Phosphatidylcholine (PtdCho) biosynthesis was examined in the sterol regulatory defective (SRD) Chinese hamster ovary (CHO) cell line SRD 6. SRD 6 cells do not display transcriptional activation of sterol-regulated genes and are cholesterol auxotrophs. Compared to CHO 7 cells (parental line from which the SRD cells were derived), incorporation of [3H]choline during a 2-h pulse into PtdCho and sphingomyelin was reduced 3- and 4.5-fold, respectively, in SRD 6 cells grown with or without cholesterol. SRD 6 cells grown in cholesterol-free medium for 24 h had 8% less phosphatidylcholine (PtdCho) mass compared to CHO 7 cells. Consistent with impaired CTP:phosphocholine cytidylyltransferase activity, [3H]choline-labeled SRD 6 cells had elevated [3H]phosphocholine and delayed conversion to [3H]PtdCho during a 2-h chase period. Compared to CHO 7 cells, cytosolic cytidylyltransferase activity was elevated 2- to 3-fold in SRD 6 cells grown in the absence of cholesterol, but activity in the total membrane fraction was normal. Immunoblot analysis confirmed that cytidylyltransferase mass was increased 2-fold in SRD 6 total cell extracts and cytosol, but not membranes. The amount of [32P]phosphate-labeled cytidylyltransferase in cytosol and membranes of SRD 6 cells were similar to controls. Likewise, cytidylyltransferase mRNA levels were not significantly different between SRD 6 and CHO 7. The defect in PtdCho synthesis in SRD 6 cells could be overcome by treatment with 150 microns oleate, such that after 5 h [3H] choline incorporation into PtdCho and phosphocholine in SRD 6 and CHO 7 cells was similar. Cholesterol auxotrophic SRD 6 cells display reduced PtdCho mass and synthesis and elevated levels of cytosolic cytidylyltransferase, defects that were only partially corrected by growth in exogenous cholesterol. These results indicate a requirement for normal cholesterol regulation and synthesis in the maintenance PtdCho levels and activity of cytidylyltransferase.
在固醇调节缺陷型(SRD)中国仓鼠卵巢(CHO)细胞系SRD 6中检测了磷脂酰胆碱(PtdCho)的生物合成。SRD 6细胞不显示固醇调节基因的转录激活,并且是胆固醇营养缺陷型。与CHO 7细胞(SRD细胞的亲本系)相比,在有或没有胆固醇的情况下生长的SRD 6细胞中,在2小时脉冲期间[3H]胆碱掺入PtdCho和鞘磷脂的量分别减少了3倍和4.5倍。在无胆固醇培养基中生长24小时的SRD 6细胞与CHO 7细胞相比,磷脂酰胆碱(PtdCho)质量少8%。与CTP:磷酸胆碱胞苷转移酶活性受损一致,[3H]胆碱标记的SRD 6细胞在2小时的追踪期内[3H]磷酸胆碱升高,向[3H]PtdCho的转化延迟。与CHO 7细胞相比,在无胆固醇条件下生长的SRD 6细胞中,胞质胞苷转移酶活性升高了2至3倍,但总膜部分的活性正常。免疫印迹分析证实,SRD 6总细胞提取物和胞质溶胶中胞苷转移酶质量增加了2倍,但膜中没有增加。SRD 6细胞胞质溶胶和膜中[32P]磷酸盐标记的胞苷转移酶量与对照相似。同样,SRD 6和CHO 7之间的胞苷转移酶mRNA水平没有显著差异。用150微摩尔油酸处理可以克服SRD 6细胞中PtdCho合成的缺陷,使得5小时后SRD 6和CHO 7细胞中[3H]胆碱掺入PtdCho和磷酸胆碱的情况相似。胆固醇营养缺陷型SRD 6细胞显示PtdCho质量和合成减少,胞质胞苷转移酶水平升高,这些缺陷仅通过外源性胆固醇生长得到部分纠正。这些结果表明,维持PtdCho水平和胞苷转移酶活性需要正常的胆固醇调节和合成。