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Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation

  • Authors:
    • Zhiwei Chen
    • Ling Yao
    • Yuanyuan Liu
    • Zheng Pan
    • Shuang Peng
    • Guoguo Wan
    • Junxiong Cheng
    • Jianwei Wang
    • Wenfu Cao
  • View Affiliations / Copyright

    Affiliations: Chongqing Key Laboratory of Traditional Chinese Medicine for Prevention and Cure of Metabolic Diseases, College of Traditional Chinese Medicine, Chongqing Medical University, Chongqing 400016, P.R. China, Department of Hematology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing 400038, P.R. China, Department of Intensive Care Unit, Chongqing Traditional Chinese Medicine Hospital, Chongqing 400021, P.R. China
    Copyright: © Chen et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3741-3750
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    Published online on: September 25, 2019
       https://doi.org/10.3892/etm.2019.8047
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Abstract

Activated hepatic stellate cells (HSCs) are the principal effectors during hepatic fibrosis, which is characterized by the accumulation of extracellular matrix. Therefore, present therapies and investigations into hepatic fibrosis mainly focus on the suppression of activated HSCs. Astragaloside IV (ASIV) is an effective constituent extracted from the plant Astragalus membranaceus and has exhibited anti‑fibrotic properties in hepatic fibrosis. However, its protective mechanism against hepatic fibrosis is not fully understood. The present study aimed to investigate the mechanistic role of ASIV on rat HSC‑T6 cells activated with platelet‑derived growth factor (PDGF)‑BB. HSC‑T6 cells were activated using PDGF‑BB and subsequently treated with ASIV (final concentrations of 20 and 40 µg/ml) for 48 h. ASIV treatment decreased the expression of α1 type I collagen, α‑smooth muscle actin and fibronectin on mRNA and protein levels, suggesting that ASIV suppresses PDGF‑BB‑induced HSC‑T6 activation. Senescence‑associated β‑galactosidase activity, p21, high‑mobility group AT‑hook 1 and p53, common biomarkers of senescence, were upregulated by ASIV treatment. In addition, the expression of telomerase reverse transcriptase was reduced. ASIV promoted apoptosis of PDGF‑BB‑activated HSC‑T6 cells. The NF‑κB signaling pathway, which controls cellular senescence and apoptosis, was demonstrated to be stimulated by ASIV by increasing p65, p52, p50 and inhibitor of NF‑κB kinase α expression levels, and by suppressing the expression of NF‑κB inhibitor α. Taken together, these results demonstrated that ASIV promoted cellular senescence and apoptosis by activating the NF‑κB pathway to suppress PDGF‑BB‑induced HSC‑T6 activation; with potential implications for the treatment of hepatic fibrosis.
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View References

1 

Sun M and Kisseleva T: Reversibility of liver fibrosis. Clin Res Hepatol Gastroenterol. 39 (Suppl 1):S60–S63. 2015. View Article : Google Scholar : PubMed/NCBI

2 

Albanis E and Friedman SL: Hepatic fibrosis. Pathogenesis and principles of therapy. Clin Liver Dis. 5:315–334, v-vi. 2001. View Article : Google Scholar : PubMed/NCBI

3 

Duarte S, Baber J, Fujii T and Coito AJ: Matrix metalloproteinases in liver injury, repair and fibrosis. Matrix Biol. 44-46:147–156. 2015. View Article : Google Scholar : PubMed/NCBI

4 

Bitto N, Liguori E and La Mura V: Coagulation, microenvironment and liver fibrosis. Cells. 7:E852018. View Article : Google Scholar : PubMed/NCBI

5 

Hernandez-Gea V and Friedman SL: Pathogenesis of liver fibrosis. Annu Rev Pathol. 6:425–456. 2011. View Article : Google Scholar : PubMed/NCBI

6 

Higashi T, Friedman SL and Hoshida Y: Hepatic stellate cells as key target in liver fibrosis. Adv Drug Deliv Rev. 121:27–42. 2017. View Article : Google Scholar : PubMed/NCBI

7 

Wong L, Yamasaki G, Johnson RJ and Friedman SL: Induction of beta-platelet-derived growth factor receptor in rat hepatic lipocytes during cellular activation in vivo and in culture. J Clin Invest. 94:1563–1569. 1994. View Article : Google Scholar : PubMed/NCBI

8 

Krizhanovsky V, Yon M, Dickins RA, Hearn S, Simon J, Miething C, Yee H, Zender L and Lowe SW: Senescence of activated stellate cells limits liver fibrosis. Cell. 134:657–667. 2008. View Article : Google Scholar : PubMed/NCBI

9 

Kong X, Feng D, Wang H, Hong F, Bertola A, Wang FS and Gao B: Interleukin-22 induces hepatic stellate cell senescence and restricts liver fibrosis in mice. Hepatology. 56:1150–1159. 2012. View Article : Google Scholar : PubMed/NCBI

10 

Zhang Z, Yao Z, Zhao S, Shao J, Chen A, Zhang F and Zheng S: Interaction between autophagy and senescence is required for dihydroartemisinin to alleviate liver fibrosis. Cell Death Dis. 8:e28862017. View Article : Google Scholar : PubMed/NCBI

11 

Lee BY, Han JA, Im JS, Morrone A, Johung K, Goodwin EC, Kleijer WJ, DiMaio D and Hwang ES: Senescence-associated beta-galactosidase is lysosomal beta-galactosidase. Aging Cell. 5:187–195. 2006. View Article : Google Scholar : PubMed/NCBI

12 

Leontieva OV and Blagosklonny MV: CDK4/6-inhibiting drug substitutes for p21 and p16 in senescence: Duration of cell cycle arrest and MTOR activity determine geroconversion. Cell Cycle. 12:3063–3069. 2013. View Article : Google Scholar : PubMed/NCBI

13 

Narita M, Narita M, Krizhanovsky V, Nuñez S, Chicas A, Hearn SA, Myers MP and Lowe SW: A novel role for high-mobility group a proteins in cellular senescence and heterochromatin formation. Cell. 126:503–514. 2006. View Article : Google Scholar : PubMed/NCBI

14 

Chien Y, Scuoppo C, Wang X, Fang X, Balgley B, Bolden JE, Premsrirut P, Luo W, Chicas A, Lee CS, et al: Control of the senescence-associated secretory phenotype by NF-κB promotes senescence and enhances chemosensitivity. Genes Dev. 25:2125–2136. 2011. View Article : Google Scholar : PubMed/NCBI

15 

Osorio FG, Lopez-Otin C and Freije JM: NF-κB in premature aging. Aging. 4:726–727. 2012. View Article : Google Scholar : PubMed/NCBI

16 

Duci SB, Arifi HM, Ahmeti HR, Zatriqi VK, Buja ZA, Hoxha ET and Mekaj AY: Outcomes of older adults with burn injury: University clinical center of kosovo. World J Plast Surg. 4:153–158. 2015.PubMed/NCBI

17 

Elmore S: Apoptosis: A review of programmed cell death. Toxicol Pathol. 35:495–516. 2007. View Article : Google Scholar : PubMed/NCBI

18 

Arur S, Uche UE, Rezaul K, Fong M, Scranton V, Cowan AE, Mohler W and Han DK: Annexin I is an endogenous ligand that mediates apoptotic cell engulfment. Dev Cell. 4:587–598. 2003. View Article : Google Scholar : PubMed/NCBI

19 

Mallat A and Lotersztajn S: Reversion of hepatic stellate cell to a quiescent phenotype: From myth to reality? J Hepatol. 59:383–386. 2013. View Article : Google Scholar : PubMed/NCBI

20 

Sun WY, Wang L, Liu H, Li X and Wei W: A standardized extract from Paeonia lactiflora and Astragalus membranaceus attenuates liver fibrosis induced by porcine serum in rats. Int J Mol Med. 29:491–498. 2012.PubMed/NCBI

21 

Liu Y, Liu J, Wu KX, Guo XR and Tang ZH: A rapid method for sensitive profiling of bioactive triterpene and flavonoid from Astragalus mongholicus and Astragalus membranaceus by ultra-pressure liquid chromatography with tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 1085:110–118. 2018. View Article : Google Scholar : PubMed/NCBI

22 

Mei M, Tang F, Lu M, He X, Wang H, Hou X, Hu J, Xu C and Han R: Astragaloside IV attenuates apoptosis of hypertrophic cardiomyocyte through inhibiting oxidative stress and calpain-1 activation. Environ Toxicol Pharmacol. 40:764–773. 2015. View Article : Google Scholar : PubMed/NCBI

23 

Hao M, Liu Y, Chen P, Jiang H and Kuang HY: Astragaloside IV protects RGC-5 cells against oxidative stress. Neural Regen Res. 13:1081–1086. 2018. View Article : Google Scholar : PubMed/NCBI

24 

Wang S, Mou J, Cui L, Wang X and Zhang Z: Astragaloside IV inhibits cell proliferation of colorectal cancer cell lines through down-regulation of B7-H3. Biomed Pharmacother. 102:1037–1044. 2018. View Article : Google Scholar : PubMed/NCBI

25 

Wang PP, Luan JJ, Xu WK, Wang L, Xu DJ, Yang CY, Zhu YH and Wang YQ: Astragaloside IV downregulates the expression of MDR1 in Bel7402/FU human hepatic cancer cells by inhibiting the JNK/cJun/AP1 signaling pathway. Mol Med Rep. 16:2761–2766. 2017. View Article : Google Scholar : PubMed/NCBI

26 

Li LC, Xu L, Hu Y, Cui WJ, Cui WH, Zhou WC and Kan LD: Astragaloside IV improves bleomycin-induced pulmonary fibrosis in rats by attenuating extracellular matrix deposition. Front Pharmacol. 8:5132017. View Article : Google Scholar : PubMed/NCBI

27 

Qian W, Cai X, Qian Q, Zhang W and Wang D: Astragaloside IV modulates TGF-β1-dependent epithelial-mesenchymal transition in bleomycin-induced pulmonary fibrosis. J Cell Mol Med. 22:4354–4364. 2018. View Article : Google Scholar : PubMed/NCBI

28 

Wan Y, Xu L, Wang Y, Tuerdi N, Ye M and Qi R: Preventive effects of astragaloside IV and its active sapogenin cycloastragenol on cardiac fibrosis of mice by inhibiting the NLRP3 inflammasome. Eur J Pharmacol. 833:545–554. 2018. View Article : Google Scholar : PubMed/NCBI

29 

Chen P, Xie Y, Shen E, Li GG, Yu Y, Zhang CB, Yang Y, Zou Y, Ge J, Chen R and Chen H: Astragaloside IV attenuates myocardial fibrosis by inhibiting TGF-β1 signaling in coxsackievirus B3-induced cardiomyopathy. Eur J Pharmacol. 658:168–174. 2011. View Article : Google Scholar : PubMed/NCBI

30 

Xu W, Shao X, Tian L, Gu L, Zhang M, Wang Q, Wu B, Wang L, Yao J, Xu X, et al: Astragaloside IV ameliorates renal fibrosis via the inhibition of mitogen-activated protein kinases and antiapoptosis in vivo and in vitro. J Pharmacol Exp Ther. 350:552–562. 2014. View Article : Google Scholar : PubMed/NCBI

31 

Wang L, Chi YF, Yuan ZT, Zhou WC, Yin PH, Zhang XM, Peng W and Cai H: Astragaloside IV inhibits renal tubulointerstitial fibrosis by blocking TGF-β/Smad signaling pathway in vivo and in vitro. Exp Biol Med (Maywood). 239:1310–1324. 2014. View Article : Google Scholar : PubMed/NCBI

32 

Liu H, Wei W, Sun WY and Li X: Protective effects of astragaloside IV on porcine-serum-induced hepatic fibrosis in rats and in vitro effects on hepatic stellate cells. J Ethnopharmacol. 122:502–508. 2009. View Article : Google Scholar : PubMed/NCBI

33 

Ping J, Li JT, Liao ZX, Shang L and Wang H: Indole-3-carbinol inhibits hepatic stellate cells proliferation by blocking NADPH oxidase/reactive oxygen species/p38MAPK pathway. Eur J Pharmacol. 650:656–662. 2011. View Article : Google Scholar : PubMed/NCBI

34 

Li X, Wang X, Han C, Wang X, Xing G, Zhou L, Li G and Niu Y: Astragaloside IV suppresses collagen production of activated hepatic stellate cells via oxidative stress-mediated p38 MAPK pathway. Free Radic Biol Med. 60:168–176. 2013. View Article : Google Scholar : PubMed/NCBI

35 

Livak KJ and Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. 25:402–408. 2001. View Article : Google Scholar : PubMed/NCBI

36 

Tsuchida T and Friedman SL: Mechanisms of hepatic stellate cell activation. Nat Rev Gastroenterol Hepatol. 14:397–411. 2017. View Article : Google Scholar : PubMed/NCBI

37 

Huang Y, Deng X and Liang J: Modulation of hepatic stellate cells and reversibility of hepatic fibrosis. Exp Cell Res. 352:420–426. 2017. View Article : Google Scholar : PubMed/NCBI

38 

de Oliveira da Silva B, Ramos LF and Moraes KCM: Molecular interplays in hepatic stellate cells: Apoptosis, senescence, and phenotype reversion as cellular connections that modulate liver fibrosis. Cell Bio Int. 41:946–959. 2017. View Article : Google Scholar

39 

Kang C, Xu Q, Martin TD, Li MZ, Demaria M, Aron L, Lu T, Yankner BA, Campisi J and Elledge SJ: The DNA damage response induces inflammation and senescence by inhibiting autophagy of GATA. Science. 349:aaa56122015. View Article : Google Scholar : PubMed/NCBI

40 

Thirukkumaran C, Shi ZQ, Thirukkumaran P, Luider J, Kopciuk K, Spurrell J, Elzinga K and Morris D: PUMA and NF-κB are cell signaling predictors of reovirus oncolysis of breast cancer. PLoS One. 12:e01682332017. View Article : Google Scholar : PubMed/NCBI

41 

Zoubek ME, Trautwein C and Strnad P: Reversal of liver fibrosis: From fiction to reality. Best Pract Res Clin Gastroenterol. 31:129–141. 2017. View Article : Google Scholar : PubMed/NCBI

42 

Rufini A, Tucci P, Celardo I and Melino G: Senescence and aging: The critical roles of p53. Oncogene. 32:5129–5143. 2013. View Article : Google Scholar : PubMed/NCBI

43 

Chen J, Pan J, Wang J, Song K, Zhu D, Huang C and Duan Y: Soluble egg antigens of schistosoma japonicum induce senescence in activated hepatic stellate cells by activation of the STAT3/p53/p21 pathway. Sci Rep. 6:309572016. View Article : Google Scholar : PubMed/NCBI

44 

Campisi J and d'Adda di Fagagna F: Cellular senescence: When bad things happen to good cells. Nat Rev Mol Cell Biol. 8:729–740. 2007. View Article : Google Scholar : PubMed/NCBI

45 

Zhao Z, Pan X, Liu L and Liu N: Telomere length maintenance, shortening, and lengthening. J Cell Physiol. 229:1323–1329. 2014. View Article : Google Scholar : PubMed/NCBI

46 

Duval F, Moreno-Cuevas JE, Gonzalez-Garza MT, Rodriguez-Montalvo C and Cruz-Vega DE: Liver fibrosis and protection mechanisms action of medicinal plants targeting apoptosis of hepatocytes and hepatic stellate cells. Adv Pharmacol Sci. 2014:3732952014.PubMed/NCBI

47 

Meng D, Li Z, Wang G, Ling L, Wu Y and Zhang C: Carvedilol attenuates liver fibrosis by suppressing autophagy and promoting apoptosis in hepatic stellate cells. Biomed Pharmacother. 108:1617–1627. 2018. View Article : Google Scholar : PubMed/NCBI

48 

Senoo T, Sasaki R, Akazawa Y, Ichikawa T, Miuma S, Miyaaki H, Taura N and Nakao K: Geranylgeranylacetone attenuates fibrogenic activity and induces apoptosis in cultured human hepatic stellate cells and reduces liver fibrosis in carbon tetrachloride-treated mice. BMC Gastroenterol. 18:342018. View Article : Google Scholar : PubMed/NCBI

49 

Kuo LM, Chen PJ, Sung PJ, Chang YC, Ho CT, Wu YH and Hwang TL: The bioactive extract of pinnigorgia sp. induces apoptosis of hepatic stellate cells via ROS-ERK/JNK-caspase-3 signaling. Mar Drugs. 16:E192018. View Article : Google Scholar : PubMed/NCBI

50 

Hu T, Fei Z and Wei N: Chemosensitive effects of astragaloside IV in osteosarcoma cells via induction of apoptosis and regulation of caspase-dependent Fas/FasL signaling. Pharmacol Rep. 69:1159–1164. 2017. View Article : Google Scholar : PubMed/NCBI

51 

Yuan W, Zhang Y, Ge Y, Yan M, Kuang R and Zheng X: Astragaloside IV inhibits proliferation and promotes apoptosis in rat vascular smooth muscle cells under high glucose concentration in vitro. Planta Med. 74:1259–1264. 2008. View Article : Google Scholar : PubMed/NCBI

52 

Childs BG, Baker DJ, Kirkland JL, Campisi J and van Deursen JM: Senescence and apoptosis: Dueling or complementary cell fates? EMBO Rep. 15:1139–1153. 2014. View Article : Google Scholar : PubMed/NCBI

53 

Xia Y, Shen S and Verma IM: NF-κB, an active player in human cancers. Cancer Immunol Res. 2:823–830. 2014. View Article : Google Scholar : PubMed/NCBI

54 

Hayden MS and Ghosh S: Regulation of NF-κB by TNF family cytokines. Semin Immunol. 26:253–266. 2014. View Article : Google Scholar : PubMed/NCBI

55 

Lee JJ, Koh KN, Park CJ, Jang S, Im HJ and Kim N: The combination of flavokawain B and daunorubicin induces apoptosis in human myeloid leukemic cells by modifying NF-κB. Anticancer Res. 38:2771–2778. 2018.PubMed/NCBI

56 

Yilmaz B and Karabay AZ: Food additive sodium benzoate (NaB) activates NFkB and induces apoptosis in HCT116 cells. Molecules. 23:E7232018. View Article : Google Scholar : PubMed/NCBI

57 

Kim CS, Choi JS, Joo SY, Bae EH, Ma SK, Lee J and Kim SW: Nicotine-induced apoptosis in human renal proximal tubular epithelial cells. PLoS One. 11:e01525912016. View Article : Google Scholar : PubMed/NCBI

58 

Ying HZ, Chen Q, Zhang WY, Zhang HH, Ma Y, Zhang SZ, Fang J and Yu CH: PDGF signaling pathway in hepatic fibrosis pathogenesis and therapeutics (Review). Mol Med Rep. 16:7879–7889. 2017. View Article : Google Scholar : PubMed/NCBI

59 

Trappoliere M, Caligiuri A, Schmid M, Bertolani C, Failli P, Vizzutti F, Novo E, di Manzano C, Marra F, Loguercio C and Pinzani M: Silybin, a component of sylimarin, exerts anti-inflammatory and anti-fibrogenic effects on human hepatic stellate cells. J Hepatol. 50:1102–1111. 2009. View Article : Google Scholar : PubMed/NCBI

60 

Paik YH, Kim JK, Lee JI, Kang SH, Kim DY, An SH, Lee SJ, Lee DK, Han KH, Chon CY, et al: Celecoxib induces hepatic stellate cell apoptosis through inhibition of Akt activation and suppresses hepatic fibrosis in rats. Gut. 58:1517–1527. 2009. View Article : Google Scholar : PubMed/NCBI

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Copy and paste a formatted citation
Spandidos Publications style
Chen Z, Yao L, Liu Y, Pan Z, Peng S, Wan G, Cheng J, Wang J and Cao W: Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation. Exp Ther Med 18: 3741-3750, 2019.
APA
Chen, Z., Yao, L., Liu, Y., Pan, Z., Peng, S., Wan, G. ... Cao, W. (2019). Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation. Experimental and Therapeutic Medicine, 18, 3741-3750. https://doi.org/10.3892/etm.2019.8047
MLA
Chen, Z., Yao, L., Liu, Y., Pan, Z., Peng, S., Wan, G., Cheng, J., Wang, J., Cao, W."Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation". Experimental and Therapeutic Medicine 18.5 (2019): 3741-3750.
Chicago
Chen, Z., Yao, L., Liu, Y., Pan, Z., Peng, S., Wan, G., Cheng, J., Wang, J., Cao, W."Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation". Experimental and Therapeutic Medicine 18, no. 5 (2019): 3741-3750. https://doi.org/10.3892/etm.2019.8047
Copy and paste a formatted citation
x
Spandidos Publications style
Chen Z, Yao L, Liu Y, Pan Z, Peng S, Wan G, Cheng J, Wang J and Cao W: Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation. Exp Ther Med 18: 3741-3750, 2019.
APA
Chen, Z., Yao, L., Liu, Y., Pan, Z., Peng, S., Wan, G. ... Cao, W. (2019). Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation. Experimental and Therapeutic Medicine, 18, 3741-3750. https://doi.org/10.3892/etm.2019.8047
MLA
Chen, Z., Yao, L., Liu, Y., Pan, Z., Peng, S., Wan, G., Cheng, J., Wang, J., Cao, W."Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation". Experimental and Therapeutic Medicine 18.5 (2019): 3741-3750.
Chicago
Chen, Z., Yao, L., Liu, Y., Pan, Z., Peng, S., Wan, G., Cheng, J., Wang, J., Cao, W."Astragaloside IV regulates NF‑κB‑mediated cellular senescence and apoptosis of hepatic stellate cells to suppress PDGF‑BB‑induced activation". Experimental and Therapeutic Medicine 18, no. 5 (2019): 3741-3750. https://doi.org/10.3892/etm.2019.8047
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