Original Article

Effect of Copper-Containing Stainless Steel on Apoptosis of Coronary Artery Smooth Muscle Cells

Abstract

Background: We aimed to investigate the effect of copper stainless steel on apoptosis of vascular smooth muscle cells in coronary artery.

Methods: The study was carried out in 2019 at Hubei University of Medicine, Xiangyang, China. The rat coronary artery smooth muscle cell was used for cell resuscitation and culture. MTT method was used to visualize cell growth curve and to detect the cell survival and growth. The incubated cells were randomly divided into copper-containing stainless-steel group, ordinary stainless-steel group, and control group. The cells were made into single cell suspension, which were intervened by experimental group and incubated in incubator with CO2 for 48 hours. TUNEL method was used to detect the apoptosis. The number of apoptotic cells in five high power fields (×200) was counted. The expression of Fas protein in three groups of cells was detected by Western blot.

Results: The growth curves of rat coronary artery smooth muscle cells showed that the OD value of the cells reached the plateau 7 days after inoculation, indicating that the cells grew well. TUNEL staining showed the apoptosis in all three groups. The apoptotic index in copper-containing group was significantly higher than that in common stainless-steel group (P <0.01). The results of the Fas protein expression level through Western blot showed that the level in the copper-containing group was significantly higher than that in the common stainless-steel group (P<0.01).

Conclusion: Copper-containing stainless steel can promote apoptosis of coronary artery smooth muscle cells. The material could prevent stent restenosis.

1. Wang QJ, Wang D, Tang CC (2015). The 5-hydroxytryptamine transporter is func-tional in human coronary artery smooth muscle cells proliferation and is regulated by Interleukin-1 beta. Int J Clin Exp Med, 8(5): 6947-56.
2. Lipskaia L, Hadri L, Le Prince P, et al (2013). SERCA2a gene transfer prevents intimal proliferation in an organ culture of hu-man internal mammary artery. Gene Ther, 20(4): 396-406.
3. Kitamura N, Hasebe T, Matsumoto T, et al (2014). Basic fibroblast growth factor as a potential stent coating material inducing endothelial cell proliferation. J Atheroscler Thromb, 21(5): 477-85.
4. Zsebo K, Yaroshinsky A, Rudy JJ, et al (2014). Long-term effects of AAV1/SERCA2a gene transfer in pa-tients with severe heart failure: analysis of recurrent cardiovascular events and mor-tality. Circ Res, 114(1): 101-8.
5. Zuniga MC, Raghuraman G, Zhou W (2018). Physiologic levels of resistin in-duce a shift from proliferation to apop-tosis in macrophage and VSMC co-culture. Surgery, 163(4): 906-11.
6. Li J, Ren L, Zhang S, et al (2015). Cu-bearing steel reduce inflammation after stent implantation. J Mater Sci Mater Med, 26(2): 1-4.
7. Qu Y, Zhang N (2018). miR-365b-3p inhib-its the cell proliferation and migration of human coronary artery smooth muscle cells by directly targeting ADAMTS1 in coronary atherosclerosis. Exp Ther Med, 16(5): 4239-45.
8. Grüntzig AR, Senning A, Siegenthaler WE (1979). Nonoperative dilatation of coro-nary-artery stenosis: percutaneous trans-luminal coronary angioplasty. N Engl J Med, 301(2): 61-8.
9. Cai F, Zeng XR, Yang Y, et al (2005). Effect of IP3 on BK channels of porcine coro-nary artery smooth muscle cells. Sheng Li Xue Bao, 57(3): 303-9.
10. Freixa X, Almasood AS, Khan SQ, et al (2013). Choice of stent and outcomes af-ter treatment of drug-eluting stent reste-nosis in highly complex lesions. Catheter Cardiovasc Interv, 81(1): E16-22.
11. Fan S, Li X, Lin J, et al (2014). Honokiol In-hibits Tumor Necrosis Factor-α-Stimulated Rat Aortic Smooth Muscle Cell Proliferation via, Caspase- and Mito-chondrial-Dependent Apoptosis. Inflam-mation, 37(1): 17-26.
12. Medema JP, Scaffidi C, Kischkel FC, et al (1997). FLICE is activated by association with the CD95 death-inducing signaling complex (DISC). EMBO J, 16 (10): 2794-804.
13. Hu S, Kim HS, Savage P, et al (1997). Activa-tion of BK (Ca) channel via endothelin ET(A) receptors in porcine coronary ar-tery smooth muscle cells. Eur J Pharmacol, 324 (2-3): 277-82.
14. Padró T, Lugano R, García-Arguinzonis M, et al (2012). LDL-induced impairment of human vascular smooth muscle cells re-pair function is reversed by HMG-CoA reductase inhibition. Plos One, 7(6): e38935.
15. Tan NY, Li JM, Stocker R, et al (2009). An-giotensin II-inducible smooth muscle cell apoptosis involves the angiotensin II Type 2 receptor,GATA-6 activation, and FasL-Fas engagement. Circ Res, 105(5): 422-30.
16. Majewski M, Ognik K, Zdunczyk P, et al (2017). Effect of dietary copper nanopar-ticles versus one copper (II) salt: Analysis of vasoreactivity in a rat model. Pharmacol Rep, 69(6): 1282-8.
17. Klevay LM (1985). Atrial thrombosis, ab-normal electrocardiograms and sudden death in mice due to copper deficiency. Atherosclerosis, 54(2): 213-24.
18. Jehle J, Tiyerili V, Adler S, et al (2020). Atheroprotective effects of 17β-oestradiol are mediated by peroxisome proliferator-activated receptor γ in human coronary artery smooth muscle cells. Arch Med Sci Atheroscler Dis, 5: e118-e126.
19. Ogita H, Isobe Y, Takaku H, et al (2001). Synthesis and structure-activity relation-ship of diarylamide derivatives as selective inhibitors of the proliferation of human coronary artery smooth muscle cells. Bioorg Med Chem Lett, 11(4): 549-51.
20. Ogita H, Isobe Y, Takaku H, et al (2002). Synthesis and structure-activity relation-ship of diarylamide urea derivatives as se-lective inhibitors of the proliferation of human coronary artery smooth muscle cells. Bioorg Med Chem, 10(6): 1865-71.
21. Zhao J, Ren L, Liu M, et al (2018). Anti-fibrotic function of Cu-bearing stainless steel for reducing recurrence of urethral stricture after stent implantation. J Biomed Mater Res B Appl Biomater, 106(5): 2019-2028
22. Li L, Pan S, Zhou X, et al (2013). Reduction of In-Stent Restenosis Risk on Nickel-Free Stainless Steel by Regulating Cell Apoptosis and Cell Cycle. Plos One, 8(4): 62193.
23. Harris AN, Hinojosa BR, Chavious MD, et al (2011). Beyond platinum: synthesis, characterization, and in vitro toxicity of Cu (II)-releasing polymer nanoparticles for potential use as a drug delivery vector. Nanoscale Res Lett, 6(1): 445.
Files
IssueVol 50 No 9 (2021) QRcode
SectionOriginal Article(s)
DOI https://doi.org/10.18502/ijph.v50i9.7055
Keywords
Copper-containing stainless steel Coronary artery Muscle cells Apoptosis Fas protein Restenosis

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Li H, Li X, Cao T, Zhu Q, Liu F, Zhou H. Effect of Copper-Containing Stainless Steel on Apoptosis of Coronary Artery Smooth Muscle Cells. Iran J Public Health. 2021;50(9):1825-1831.