Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1980 Sep 1;86(3):810–819. doi: 10.1083/jcb.86.3.810

Apparent coordination of the biosynthesis of lipids in cultured cells: its relationship to the regulation of the membrane sterol:phospholipid ratio and cell cycling

PMCID: PMC2110678  PMID: 6157695

Abstract

The coordination of the syntheses of the several cellular lipid classes with one another and with cell cycle control were investigated in proliferating L6 myoblasts and fibroblasts (WI-38 and CEF). Cells cultured in lipid-depleted medium containing one of two inhibitors of hydroxymethylglutaryl-CoA reductase, 25-hydroxycholesterol or compactin, display a rapid, dose-dependent inhibition of cholesterol synthesis. Inhibition of the syntheses of each of the other lipid classes is first apparent after the rate of sterol synthesis is depressed severalfold. 24 h after the addition of the inhibitor, the syntheses of DNA, RNA, and protein also decline. The inhibition of sterol synthesis leads to a threefold reduction in the sterol:phospholipid ratio that parallels the development of proliferative and G1 cell cycle arrests and alterations in cellular morphology. All of these responses are reversed upon reinitiation of cholesterol synthesis or addition of exogenous cholesterol. A comparison of the timing of these responses with respect to the development of the G1 arrest indicates that the primary factor limiting cell cycling is the availability of cholesterol provided either from an exogenous source or by de novo synthesis. The G1 arrest appears to be responsible for the general inhibition of macromolecular synthesis in proliferating cells treated with 25-hydroxycholesterol. In contrast, the apparent coordinated inhibition of lipid synthesis is not a consequence of the G1 arrest but may in fact give rise to it. Sequential inhibition of lipid syntheses is also observed in cycling cells when the synthesis of choline-containing lipids is blocked by choline deprivation and is observed in association with G1 arrests caused by confluence or differentiation. In the nonproliferating cells, the syntheses of lipid and protein do not appear coupled.

Full Text

The Full Text of this article is available as a PDF (1.1 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BAILEY J. M. LIPID METABOLISM IN CULTURED CELLS. V. COMPARATIVE LIPID NUTRITION IN SERUM AND IN LIPID-FREE CHEMICALLY DEFINED MEDIUM. Proc Soc Exp Biol Med. 1964 Mar;115:747–750. doi: 10.3181/00379727-115-29026. [DOI] [PubMed] [Google Scholar]
  2. BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
  3. Bischoff R., Holtzer H. Mitosis and the processes of differentiation of myogenic cells in vitro. J Cell Biol. 1969 Apr;41(1):188–200. doi: 10.1083/jcb.41.1.188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brown M. S., Faust J. R., Goldstein J. L., Kaneko I., Endo A. Induction of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in human fibroblasts incubated with compactin (ML-236B), a competitive inhibitor of the reductase. J Biol Chem. 1978 Feb 25;253(4):1121–1128. [PubMed] [Google Scholar]
  5. Cornell R., Grove G. L., Rothblat G. H., Horwitz A. F. Lipid requirement for cell cycling. The effect of selective inhibition of lipid synthesis. Exp Cell Res. 1977 Oct 15;109(2):299–307. doi: 10.1016/0014-4827(77)90009-x. [DOI] [PubMed] [Google Scholar]
  6. Freeman C. P., West D. Complete separation of lipid classes on a single thin-layer plate. J Lipid Res. 1966 Mar;7(2):324–327. [PubMed] [Google Scholar]
  7. HAVEL R. J., EDER H. A., BRAGDON J. H. The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum. J Clin Invest. 1955 Sep;34(9):1345–1353. doi: 10.1172/JCI103182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hatten M. E., Horwitz A. F., Burger M. M. The influence of membrane lipids on the proliferation of transformed and untransformed cell lines. Exp Cell Res. 1977 Jun;107(1):31–34. doi: 10.1016/0014-4827(77)90382-2. [DOI] [PubMed] [Google Scholar]
  9. Horwitz A. F., Wight A., Ludwig P., Cornell R. Interrelated lipid alterations and their influence on the proliferation and fusion of cultured myogenic cells. J Cell Biol. 1978 May;77(2):334–357. doi: 10.1083/jcb.77.2.334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Howard B. V. Acetate as a carbon source for lipid synthesis in cultured cells. Biochim Biophys Acta. 1977 Jul 20;488(1):145–151. doi: 10.1016/0005-2760(77)90132-1. [DOI] [PubMed] [Google Scholar]
  11. James M. J., Kandutsch A. A. Inter-relationships between dolichol and sterol synthesis in mammalian cell cultures. J Biol Chem. 1979 Sep 10;254(17):8442–8446. [PubMed] [Google Scholar]
  12. Kandutsch A. A., Chen H. W. Consequences of blocked sterol synthesis in cultured cells. DNA synthesis and membrane composition. J Biol Chem. 1977 Jan 25;252(2):409–415. [PubMed] [Google Scholar]
  13. Kandutsch A. A., Chen H. W. Inhibition of sterol synthesis in cultured mouse cells by 7alpha-hydroxycholesterol, 7beta-hydroxycholesterol, and 7-ketocholesterol. J Biol Chem. 1973 Dec 25;248(24):8408–8417. [PubMed] [Google Scholar]
  14. Kent C., Schimmel S. D., Vagelos P. R. Lipid composition of plasma membranes from developing chick muscle cells in culture. Biochim Biophys Acta. 1974 Sep 19;360(3):312–321. doi: 10.1016/0005-2760(74)90061-7. [DOI] [PubMed] [Google Scholar]
  15. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  16. Limanek J. S., Chin J., Chang T. Y. Mammalian cell mutant requiring cholesterol and unsaturated fatty acid for growth. Proc Natl Acad Sci U S A. 1978 Nov;75(11):5452–5456. doi: 10.1073/pnas.75.11.5452. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Marsh J. B. Lipoproteins in a nonrecirculating perfusate of rat liver. J Lipid Res. 1974 Nov;15(6):544–550. [PubMed] [Google Scholar]
  18. Mills J. T., Adamany A. M. Impairment of dolichyl saccharide synthesis and dolichol-mediated glycoprotein assembly in the aortic smooth muscle cell in culture by inhibitors of cholesterol biosynthesis. J Biol Chem. 1978 Aug 10;253(15):5270–5273. [PubMed] [Google Scholar]
  19. Rein A., Rubin H. Effects of local cell concentrations upon the growth of chick embryo cells in tissue culture. Exp Cell Res. 1968 Mar;49(3):666–678. doi: 10.1016/0014-4827(68)90213-9. [DOI] [PubMed] [Google Scholar]
  20. SINGLETON W. S., GRAY M. S., BROWN M. L., WHITE J. L. CHROMATOGRAPHICALLY HOMOGENEOUS LECITHIN FROM EGG PHOSPHOLIPIDS. J Am Oil Chem Soc. 1965 Jan;42:53–56. doi: 10.1007/BF02558256. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES