DOI QR코드

DOI QR Code

Ginsenoside Rb2 Upregulates the Low Density Lipoprotein Receptor Gene Expression through the Activation of the Sterol Regulated Element Binding Protein Maturation in HepG2 Cells

  • Lim, Grewo (Department of Biochemistry, College of Medicine, Konkuk University) ;
  • Lee, Hyunil (Department of Biochemistry, College of Medicine, Konkuk University) ;
  • Kim, Eun-Ju (Department of Biochemistry, College of Medicine, Konkuk University) ;
  • Noh, Yun-Hee (Department of Biochemistry, College of Medicine, Konkuk University) ;
  • Ro, Youngtae (Department of Biochemistry, College of Medicine, Konkuk University) ;
  • Koo, Ja-Hyun (Department of Biochemistry, College of Medicine, Konkuk University)
  • Published : 2005.12.01

Abstract

Ginsenosides, a group of Panax ginseng saponins, exert the lowering effects of plasma cholesterol levels in animals. We had reported earlier that ginsenoside Rb2 upregulate low-density lipoprotein receptor (LDLR) expression via a mechanism that is dependent of the activation of sterol response element binding protein 2 (SREBP-2) expression. This study was conducted to determine the effects of ginsenoside Rb2 on the expression of the hepatic LDLR expression at cellular levels using HepG2 cells, and to evaluate whether the sterol response element binding protein 1 (SREBP-l) was involved in the regulation of LDLR expression. Incubation of HepG2 cells in serum-free medium supplemented with cholesterol $(10{\mu}g/ml)$ for 8 hours decreased the mRNAs of LDLR mRNA by $12\%$ and SREBP-l mRNA by $35\%$. Ginsenoside Rb2 antagonized the repressive effects of cholesterol and increased both LDLR and SREBP-l mRNA expression to 1.5- and 2-fold, respectively. Furthermore, Western blot and confocal microscopic analyses with SREBP-l polyclonal antibody revealed that ginsenoside Rb2 enhanced the maturation of the SREBP-1 from the inactive precursor form in ER membrane to the active transcription factor form in nucleus. These results suggest that ginsenoside Rb2 upregulates LDLR expression via a mechanism that is dependent of the activation of not only SREBP-2 expression, but also SREBP-1 expression and maturation, and also indicate that the pharmacological value of ginsenoside Rb2 may be distinguished from that of lovastatin which is reported that it upregulate LDLR through SREBP-2 only, not through SREBP-1.

Keywords

References

  1. Sato, R. and Takano, T. : Regulation of intracellular choles- terol metabolism. Cell Struct Funct. 20, 421-427 (1995) https://doi.org/10.1247/csf.20.421
  2. Dujovne, C.A. and Harris, W.S. : The pharmacological treatment of dyslipidemia. Annu Rev Pharmacol Toxicol. 29, 265-288 (1989) https://doi.org/10.1146/annurev.pa.29.040189.001405
  3. Brown, M.S., Kovanen, P.T. and Goldstein, J.L. : Regulation of plasma cholesterol by lipoprotein receptors. Science. 212, 628-635 (1981) https://doi.org/10.1126/science.6261329
  4. Kang, S. and Davis, R.A. : Cholesterol and hepatic lipoprotein assembly and secretion. Biochim Biophys Acta. 1529, 223-230 (2000) https://doi.org/10.1016/S1388-1981(00)00151-7
  5. Nimpf, J. and Schneider, W.J. : From cholesterol transport to signal transduction: low density lipoprotein receptor, very low density lipoprotein receptor, and apolipoprotein E receptor-2. Biochim Biophys Acta. 1529, 287-298 (2000) https://doi.org/10.1016/S1388-1981(00)00155-4
  6. Rajendran, S. and Deepalakshmi, P.D. : Parasakthy K, Devaraj H, Devaraj SN. Effect of tincture of Crataegus on the LDLreceptor activity of hepatic plasma membrane of rats fed an atherogenic diet. Atherosclerosis. 123,235-241 (1996) https://doi.org/10.1016/0021-9150(96)05813-3
  7. Hua, X., Yokoyama, C., Wu, J., Briggs, M.R., Brown, MS., Goldstein, J.L. and Wang, X. : SREBP-2, a second basichelix-loop-helix-leucine zipper protein that stimulates transcription by binding to a sterol regulatory element. Proc Natl Acad Sci USA. 90,11603-11607 (1993) https://doi.org/10.1073/pnas.90.24.11603
  8. Yokoyama, C., Wang, X., Briggs, M.R., Admon, A., Wu, J., Hua, X., Goldstein, J.L. and Brown, M.S.: SREBP-I, a basic-helix-loop-helix-leucine zipper protein that controls transcription of the low density lipoprotein receptor gene. Cell. 75,187-197 (1993) https://doi.org/10.1016/S0092-8674(05)80095-9
  9. Brown, M.S. and Goldstein, J.L.: The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor. Cell. 89, 331-340 (1997) https://doi.org/10.1016/S0092-8674(00)80213-5
  10. Goldstein, J.L. : Brown MS. Regulation of the mevalonate pathway. Nature. 343, 425-430 (1990) https://doi.org/10.1038/343425a0
  11. Yun, T.K. and Choi, SY Preventive effect of ginseng intake against various human cancers: a case-control study on 1987 pairs. Cancer Epidemiol Biomarkers Prev. 4, 401-408 (1995)
  12. Yun, T.K. and Choi, S.Y. : Non-organ specific cancer prevention of ginseng: a prospective study in Korea. Int J Epidemiol. 27, 359-364 (1998) https://doi.org/10.1093/ije/27.3.359
  13. Wakabayashi, C., Hasegawa, H., Murata, J. and Saiki, I. : In vivo antimetastatic action of ginseng protopanaxadiol saponins is based on their intestinal bacterial metabolites after oral administration. Oncol Res. 9,411-417 (1997)
  14. Joo, C.N. : Role of ginsenosides as bioreactor in lipid metabolism. J Nutr Sci Vitaminol (Tokyo). 298-301 (1992)
  15. Kang, S.Y., Kim, S.H., Schini, V.B. and Kim, N.D. : Dietary ginsenosides improve endothelium-dependent relaxation in the thoracic aorta of hypercholesterolemic rabbit. Gen Pharmacol. 26,483-487 (1995) https://doi.org/10.1016/0306-3623(95)94002-X
  16. Yokozawa, T., Kobayashi, T., Oura, H. and Kawashima, Y. : Hyperlipemia-improving effects of ginsenoside-Rb2 in strepto-zotocin-diabetic rats. Chem Pharm Bull (Tokyo). 33, 3893-3898 (1985) https://doi.org/10.1248/cpb.33.3893
  17. Gommori, K., Miyamoto, F., Shibata, Y., Higashi, T. and Sanada, S. : Effect of ginseng saponins on cholesterol metabolism. II. Effect of ginsenosides on cholesterol synthesis by liver slice. Chem Pharm Bull (Tokyo). 24, 2985-2987 (1976) https://doi.org/10.1248/cpb.24.2985
  18. Ikehara, M., Shibata, Y, Higashi, T., Sanada, S. and Shoji, J. : Effect of ginseng saponins on cholesterol metabolism. III. Effect of ginsenoside-Rb on cholesterol synthesis in rats fed on high-fat diet. Chem Pharm Bull (Tokyo). 26, 2844-2854 (1978) https://doi.org/10.1248/cpb.26.2844
  19. Sakakibara, K., Shibata, Y, Higashi, T., Sanada, S. and Shoji, J. : Effect of ginseng saponins on cholesterol metabolism. I. The level and the synthesis of serum and liver cholesterol in rats treated with ginsenosides. Chem Pharm Bull (Tokyo). 23, 1009-1016 (1975) https://doi.org/10.1248/cpb.23.1009
  20. Lim, G., Lee, H.I., Kim, E.J., Ro, Y.T., Noh, Y.H. and Koo, J.H. : The mechanism of LDL receptor up-regulation by ginsenoside Rb2 in HepG2 cultured under enriched cholesterol condition. J. Ginseng Res. 28(2), 87-93 (2004), (in Korean) https://doi.org/10.5142/JGR.2004.28.2.087
  21. Havekes, L.M, de Wit, E.C. and Princen, H.M. Cellular free cholesterol in Hep G2 cells is only partially available for down-regulation of low-density-lipoprotein receptor activity. Biochem J. 247, 739-746 (1987) https://doi.org/10.1042/bj2470739
  22. Chomczynski, P. and Sacchi, N.: Single-step method of RNA isolation by acid guanidinium thiocyanate-phenolchloroform extraction. Anal Biochem. 162, 156-159 (1987)
  23. Hua, X., Sakai, J., Brown, M.S. and Goldstein, J.L. : Regulated cleavage of sterol regulatory element binding proteins requires sequences on both sides of the endoplasmic reticulum membrane. J Biol Chem. 271, 10379-10384 (1996) https://doi.org/10.1074/jbc.271.17.10379
  24. Harwood, H.J. Jr, Chandler, C.E., Pellarin, L.D., Bangerter, F.W., Wilkins, R.W, Long, C.A, Cosgrove, P.G, Malinow, M.R., Marzetta, C.A., Pettini, J.L., Savoy, Y.E. and Mayne, J.T. : Pharmacologic consequences of cholesterol absorption inhibition: alteration in cholesterol metabolism and reduction in plasma cholesterol concentration induced by the synthetic saponin beta-tigogenin cellobioside (CP-88818; tiqueside). J Lipid Res. 34, 377-395 (1993)
  25. Morehouse, L.A., Bangerter, F.W., DeNinno, M.P., Inskeep, P.B., McCarthy, P.A., Pettini, J.L., Savoy, YE., Sugarman, E.D., Wilkins, R.W., Wilson, T.C., Woody, H.A., Zaccaro, L.M. and Chandler, C.E. : Comparison of synthetic saponin cholesterol absorption inhibitors in rabbits: evidence for a non-stoichiometric, intestinal mechanism of action. J Lipid Res. 40, 464-474 (1999)
  26. Briggs, M.R., Yokoyama, C., Wang, X. and Brown, M.S. : Goldstein JL. Nuclear protein that binds sterol regulatory element of low density lipoprotein receptor promoter. I. Identification of the protein and delineation of its target nucleotide sequence. J Biol Chem. 268, 14490-14496 (1993)
  27. Field, F.J., Born, E., Murthy, S. and Mathur, S.N. Gene expression of sterol regulatory element-binding proteins in hamster small intestine. J Lipid Res. 42, 1-8 (2001)
  28. Smith, J.R., Osborne, T.E, Goldstein, J.L. and Brown, M.S. Identification of nucleotides responsible for enhancer activity of sterol regulatory element in low density lipoprotein receptor gene, J Biol Chem. 265,2306-2310 (1990)
  29. Bursill, C., Roach, P.D., Bottema, C.D. and Pal, S. : Green tea upregulates the low-density lipoprotein receptor through the sterol-regulated element binding Protein in HepG2 liver cells. J Agric Food Chem. 49, 5639-5645 (2001) https://doi.org/10.1021/jf010275d
  30. Yu-Poth, S., Yin, D., Zhao, G, Kris-Etherton, P.M., Etherton, T.D. : Conjugated linoleic acid upregulates LDL receptor gene expression in HepG2 cells. J Nutr. 134, 68-71 (2004)
  31. Shimano, H.: Sterol regulatory element-binding proteins (SREBPs): transcriptional regulators of lipid synthetic genes. Prog Lipid Res. 40, 439-452 (2001) https://doi.org/10.1016/S0163-7827(01)00010-8
  32. Sakai, J., Nohturfft, A., Cheng, D., Ho, Y.K., Brown, M.S., Goldstein, J.L.: Identification of complexes between the COOH-terminal domains of sterol regulatory element-binding proteins (SREBPs) and SREBP cleavage-activating protein. J Biol Chem. 272, 20213-20221 (1997) https://doi.org/10.1074/jbc.272.32.20213
  33. Sakai, L, Nohturfft, A., Goldstein, J.L., Brown, M.S. : Cleavage of sterol regulatory element-binding proteins (SREBPs) at site-1 requires interaction with SREBP cleavage-activating protein. Evidence from in vivo competition studies. J Biol Chem. 273, 5785-5793 (1998) https://doi.org/10.1074/jbc.273.10.5785
  34. Espenshade, P.J, Cheng, D., Goldstein, J.L., Brown, M.S. : Autocatalytic processing of site-l protease removes propeptide and permits cleavage of sterol regulatory element-binding proteins. J Biol Chem. 274, 22795-22804 (1999) https://doi.org/10.1074/jbc.274.32.22795
  35. Nagoshi, E., Imamoto, N., Sato, R. and Yoneda, Y. : Nuclear import of sterol regulatory element-binding protein-2, a basic helix-loop-helix-leucine zipper (bHLH-Zip)-containing transcription factor, occurs through the direct interaction of importin beta with HLH-Zip. Mol Biol Cell. 10, 2221-2233 (1999) https://doi.org/10.1091/mbc.10.7.2221
  36. Koo, J.H., Noh, Y.H. and Lim, G. : Studies on the mechanism of the preventive effects of Korean ginseng components on hypercholesterolemia. The effects on the cholesterol content, the LDL-receptor and the enzymes related to cholesterol metabolism in Hep G2 cells cultured in cholesterol rich medium. Proceedings of '97 Korea-Japan Ginseng Symposium. pp.91-107 (1997), (in Korean)