TY - JOUR
T1 - Ganoderma lucidum polysaccharides prevent platelet-derived growth factor-stimulated smooth muscle cell proliferation in vitro and neointimal hyperplasia in the endothelial-denuded artery in vivo
AU - Wang, Shu-Huei
AU - Liang, Chan-Jung
AU - Weng, Yu-Wen
AU - Chen, Yung-Hsiang
AU - Hsu, Hsien-Yeh
AU - Chien, Hsiung-Fei
AU - Tsai, Jaw-Shiun
AU - Tseng, Ying-Chin
AU - Li, Chi-Yuan
AU - Chen, Yuh-Lien
N1 - 被引用次數:6
Export Date: 16 March 2016
CODEN: JCLLA
通訊地址: Chen, Y.-L.; Department of Anatomy and Cell Biology, College of Medicine, National Taiwan University, No. 1, Section 1, Ren-Ai Rd, Taipei 100, Taiwan; 電子郵件: [email protected]
化學物質/CAS: Janus kinase, 161384-16-3; cyclin dependent kinase 4, 147014-97-9; protein p21, 85306-28-1; Drugs, Chinese Herbal; Lipopolysaccharides; MAP Kinase Kinase 4, 2.7.12.2; Platelet-Derived Growth Factor; Polysaccharides
參考文獻: Andres, V., Castro, C., Antiproliferative strategies for the treatment of vascular proliferative disease (2003) Curr Vasc Pharmacol, 1, pp. 85-98; Desbois-Mouthon, C., Cadoret, A., Blivet-Van Eggelpoel, M.J., Bertrand, F., Caron, M., Atfi, A., Cherqui, G., Capeau, J., Insulin-mediated cell proliferation and survival involve inhibition of c-Jun N-terminal kinases through a phosphatidylinositol 3-kinase- and mitogen-activated protein kinase phosphatase-1-dependent pathway (2000) Endocrinology, 141, pp. 922-931; Dudhgaonkar, S., Thyagarajan, A., Sliva, D., Suppression of the inflammatory response by triterpenes isolated from the mushroom Ganoderma lucidum (2009) Int Immunopharmacol, 9, pp. 1272-1280; Dzau, V.J., Braun-Dullaeus, R.C., Sedding, D.G., Vascular proliferation and atherosclerosis: New perspectives and therapeutic strategies (2002) Nat Med, 8, pp. 1249-1256; Evans, S., Dizeyi, N., Abrahamsson, P.A., Persson, J., The effect of a novel botanical agent TBS-101 on invasive prostate cancer in animal models (2009) Anticancer Res, 29, pp. 3917-3924; Gao, Y., Gao, H., Chan, E., Tang, W., Xu, A., Yang, H., Huang, M., Zhou, S., Antitumor activity and underlying mechanisms of ganopoly, the refined polysaccharides extracted from Ganoderma lucidum, in mice (2005) Immunol Invest, 34, pp. 171-198; Ghosh, S.S., Gehr, T.W., Ghosh, S., Fakhry, I., Sica, D.A., Lyall, V., Schoolwerth, A.C., PPARgamma ligand attenuates PDGF-induced mesangial cell proliferation: Role of MAP kinase (2003) Kidney Int, 64, pp. 52-62; Golias, C.H., Charalabopoulos, A., Charalabopoulos, K., Cell proliferation and cell cycle control: A mini review (2004) Int J Clin Pract, 58, pp. 1134-1141; Heldin, C.H., Westermark, B., Mechanism of action and in vivo role of platelet-derived growth factor (1999) Physiol Rev, 79, pp. 1283-1316; Hsu, H.Y., Hua, K.F., Lin, C.C., Lin, C.H., Hsu, J., Wong, C.H., Extract of Reishi polysaccharides induces cytokine expression via TLR4-modulated protein kinase signaling pathways (2004) J Immunol, 173, pp. 5989-5999; Ishizawa, K., Izawa-Ishizawa, Y., Ohnishi, S., Motobayashi, Y., Kawazoe, K., Hamano, S., Tsuchiya, K., Tamaki, T., Quercetin glucuronide inhibits cell migration and proliferation by platelet-derived growth factor in vascular smooth muscle cells (2009) J Pharmacol Sci, 109, pp. 257-264; Jiang, J., Slivova, V., Harvey, K., Valachovicova, T., Sliva, D., Ganoderma lucidum suppresses growth of breast cancer cells through the inhibition of Akt/NF-kappaB signaling (2004) Nutr Cancer, 49, pp. 209-216; Jiang, J., Slivova, V., Sliva, D., Ganoderma lucidum inhibits proliferation of human breast cancer cells by down-regulation of estrogen receptor and NF-kappaB signaling (2006) Int J Oncol, 29, pp. 695-703; Kim, H.S., Cho, H.J., Park, S.J., Park, K.W., Chae, I.H., Oh, B.H., Park, Y.B., Lee, M.M., The essential role of p21 in radiation-induced cell cycle arrest of vascular smooth muscle cell (2004) J Mol Cell Cardiol, 37, pp. 871-880; Lin, S.J., Shyue, S.K., Hung, Y.Y., Chen, Y.H., Ku, H.H., Chen, J.W., Tam, K.B., Chen, Y.L., Superoxide dismutase inhibits the expression of vascular cell adhesion molecule-1 and intracellular cell adhesion molecule-1 induced by tumor necrosis factor-alpha in human endothelial cells through the JNK/p38 pathways (2005) Arterioscler Thromb Vasc Biol, 25, pp. 334-340; Lin, C.Y., Chen, Y.H., Hsu, H.Y., Wang, S.H., Liang, C.J., Kuan, I.I., Wu, P.J., Chen, Y.L., Ganoderma lucidum polysaccharides attenuate endotoxin-induced intercellular cell adhesion molecule-1 expression in cultured smooth muscle cells and in the neointima in mice (2010) J Agric Food Chem, 58, pp. 9563-9571; Miyazaki, T., Nishijima, M., Studies on fungal polysaccharides. XXVII. Structural examination of a water-soluble, antitumor polysaccharide of Ganoderma lucidum (1981) Chem Pharm Bull, 29, pp. 3611-3616; Moon, S.K., Kim, H.M., Lee, Y.C., Kim, C.H., Disialoganglioside (GD3) synthase gene expression suppresses vascular smooth muscle cell responses via the inhibition of ERK1/2 phosphorylation, cell cycle progression, and matrix metalloproteinase-9 expression (2004) J Biol Chem, 279, pp. 33063-33070; Ross, R., Cell biology of atherosclerosis (1995) Annu Rev Physiol, 57, pp. 791-804; Sata, M., Maejima, Y., Adachi, F., Fukino, K., Saiura, A., Sugiura, S., Aoyagi, T., Nagai, R., A mouse model of vascular injury that induces rapid onset of medial cell apoptosis followed by reproducible neointimal hyperplasia (2000) J Mol Cell Cardiol, 32, pp. 2097-2104; Shankland, S.J., Wolf, G., Cell cycle regulatory proteins in renal disease: Role in hypertrophy, proliferation, and apoptosis (2000) Am J Physiol Renal Physiol, 278, pp. F515-F529; Shiao, M.S., Natural products of the medicinal fungus Ganoderma lucidum: Occurrence, biological activities, and pharmacological functions (2003) Chem Rec, 3, pp. 172-180; Sliva, D., Labarrere, C., Slivova, V., Sedlak, M., Lloyd Jr., F.P., Ho, N.W., Ganoderma lucidum suppresses motility of highly invasive breast and prostate cancer cells (2002) Biochem Biophys Res Commun, 298, pp. 603-612; Sun, J., He, H., Xie, B.J., Novel antioxidant peptides from fermented mushroom Ganoderma lucidum (2004) J Agric Food Chem, 52, pp. 6646-6652; Thyagarajan, A., Jiang, J., Hopf, A., Adamec, J., Sliva, D., Inhibition of oxidative stress-induced invasiveness of cancer cells by Ganoderma lucidum is mediated through the suppression of interleukin-8 secretion (2006) Int J Mol Med, 18, pp. 657-664; Uchida, K., Sasahara, M., Morigami, N., Hazama, F., Kinoshita, M., Expression of platelet-derived growth factor B-chain in neointimal smooth muscle cells of balloon injured rabbit femoral arteries (1996) Atherosclerosis, 124, pp. 9-23; Wang, S.Y., Hsu, M.L., Hsu, H.C., Tzeng, C.H., Lee, S.S., Shiao, M.S., Ho, C.K., The anti-tumor effect of Ganoderma lucidum is mediated by cytokines released from activated macrophages and T lymphocytes (1997) Int J Cancer, 70, pp. 699-705; Wang, Y.Y., Khoo, K.H., Chen, S.T., Lin, C.C., Wong, C.H., Lin, C.H., Studies on the immuno-modulating and antitumor activities of Ganoderma lucidum (Reishi) polysaccharides: Functional and proteomic analyses of a fucose-containing glycoprotein fraction responsible for the activities (2002) Bioorg Med Chem, 10, pp. 1057-1062; Wang, G.J., Huang, Y.J., Chen, D.H., Lin, Y.L., Ganoderma lucidum extract attenuates the proliferation of hepatic stellate cells by blocking the PDGF receptor (2009) Phytother Res, 23, pp. 833-839; Xie, J.T., Wang, C.Z., Wicks, S., Yin, J.J., Kong, J., Li, J., Li, Y.C., Yuan, C.S., Ganoderma lucidum extract inhibits proliferation of SW 480 human colorectal cancer cells (2006) Exp Oncol, 28, pp. 25-29; Zhan, Y., Kim, S., Izumi, Y., Izumiya, Y., Nakao, T., Miyazaki, H., Iwao, H., Role of JNK, p38, and ERK in platelet-derived growth factor-induced vascular proliferation, migration, and gene expression (2003) Arterioscler Thromb Vasc Biol, 23, pp. 795-801
PY - 2012
Y1 - 2012
N2 - Ganoderma lucidum is used in traditional Chinese medicine to prevent or treat a variety of diseases, including cardiovascular disorders. We previously demonstrated that a glucan-containing extract of Reishi polysaccharides (EORP) has the potent anti-inflammatory action of reducing ICAM-1 expression in lipopolysaccharide (LPS)-treated human aortic smooth muscle cells (HASMCs) and LPS-treated mice. In the present study, we examined whether EORP inhibited platelet-derived growth factor-BB (PDGF)-stimulated HASMC proliferation and the mechanism involved. EORP dose-dependently reduced cell numbers and DNA synthesis of PDGF-treated HASMCs in vitro. EORP also arrested cell cycle progression in the G0/G1 phase, and this was associated with decreased expression of cyclin D1, cyclin E, CDK2, CDK4, and p21Cip1 and upregulation of the cyclin-dependent kinase inhibitor p27Kip1. The anti-proliferative effect of EORP was partly mediated by downregulation of PDGF-induced JNK phosphorylation. In in vivo studies, the femoral artery of C57BL/6 mice was endothelial-denuded and the mice were fed a diet containing 100mg/kg/day of EORP. On day 14, both cell proliferation (proliferating cell nuclear antigen-positive cells) in the neointima and the neointima/media area ratio (0.67±0.03 vs. 1.46±0.30) were significantly reduced. Our data show that EORP interferes with the mitogenic activation of JNK, preventing entry of HASMCs into the cell cycle in vitro and reducing cell proliferation in the neointima and decreasing the neointimal area in vivo. Thus, EORP may represent a safe and effective novel approach to the prevention and treatment of vascular proliferative diseases. © 2011 Wiley Periodicals, Inc.
AB - Ganoderma lucidum is used in traditional Chinese medicine to prevent or treat a variety of diseases, including cardiovascular disorders. We previously demonstrated that a glucan-containing extract of Reishi polysaccharides (EORP) has the potent anti-inflammatory action of reducing ICAM-1 expression in lipopolysaccharide (LPS)-treated human aortic smooth muscle cells (HASMCs) and LPS-treated mice. In the present study, we examined whether EORP inhibited platelet-derived growth factor-BB (PDGF)-stimulated HASMC proliferation and the mechanism involved. EORP dose-dependently reduced cell numbers and DNA synthesis of PDGF-treated HASMCs in vitro. EORP also arrested cell cycle progression in the G0/G1 phase, and this was associated with decreased expression of cyclin D1, cyclin E, CDK2, CDK4, and p21Cip1 and upregulation of the cyclin-dependent kinase inhibitor p27Kip1. The anti-proliferative effect of EORP was partly mediated by downregulation of PDGF-induced JNK phosphorylation. In in vivo studies, the femoral artery of C57BL/6 mice was endothelial-denuded and the mice were fed a diet containing 100mg/kg/day of EORP. On day 14, both cell proliferation (proliferating cell nuclear antigen-positive cells) in the neointima and the neointima/media area ratio (0.67±0.03 vs. 1.46±0.30) were significantly reduced. Our data show that EORP interferes with the mitogenic activation of JNK, preventing entry of HASMCs into the cell cycle in vitro and reducing cell proliferation in the neointima and decreasing the neointimal area in vivo. Thus, EORP may represent a safe and effective novel approach to the prevention and treatment of vascular proliferative diseases. © 2011 Wiley Periodicals, Inc.
KW - cyclin D1
KW - cyclin dependent kinase 4
KW - cyclin dependent kinase inhibitor 1B
KW - cyclin E
KW - Janus kinase
KW - plant extract
KW - platelet derived growth factor
KW - protein p21
KW - reishi polysaccharide
KW - unclassified drug
KW - animal cell
KW - animal experiment
KW - animal model
KW - animal tissue
KW - article
KW - cell count
KW - cell cycle G0 phase
KW - cell cycle G1 phase
KW - cell cycle progression
KW - cell proliferation
KW - cell viability
KW - controlled study
KW - diet
KW - DNA synthesis
KW - endothelium
KW - enzyme activation
KW - enzyme phosphorylation
KW - erythrocyte
KW - femoral artery
KW - Ganoderma lucidum
KW - human
KW - human cell
KW - hyperplasia
KW - in vitro study
KW - in vivo study
KW - male
KW - mitogenesis
KW - mouse
KW - neointimal hyperplasia
KW - nonhuman
KW - priority journal
KW - protein expression
KW - smooth muscle fiber
KW - upregulation
KW - Animals
KW - Aorta
KW - Cell Cycle
KW - Cell Death
KW - Cell Proliferation
KW - Drugs, Chinese Herbal
KW - Gene Knockdown Techniques
KW - Humans
KW - Lipopolysaccharides
KW - Male
KW - MAP Kinase Kinase 4
KW - Mice
KW - Mice, Inbred C57BL
KW - Myocytes, Smooth Muscle
KW - Neointima
KW - Phosphorylation
KW - Platelet-Derived Growth Factor
KW - Polysaccharides
KW - Reishi
KW - Mus
U2 - 10.1002/jcp.23053
DO - 10.1002/jcp.23053
M3 - Article
SN - 0021-9541
VL - 227
SP - 3063
EP - 3071
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 8
ER -