Skip to main content
Log in

The Study on Polymorphism of TrxR and Nrf2/HO-1 Signaling Pathway in Kaschin-Beck Disease

  • Published:
Biological Trace Element Research Aims and scope Submit manuscript

Abstract

Kaschin-Beck disease (KBD) is an endemic, chronic, and degenerative osteoarthropathy, which seriously impairs the quality of patients’ life. We detected the expression of TrxR by ELISA and found that TrxR was lower in KBD than in normal control group significantly (P < 0.001); this result indicated that TrxR must be related to KBD. We retrieved cSNPs in NCBI SNP database and used three bioinformatics programmers, including SIFT, PolyPhen, and SNP3d, to help select the researched nsSNP. Then, we used PCR-RFLP to analyze the relationship between the SNP site rs5746841 in TrxR2 gene and susceptibility of KBD and detected the expression of Nrf2 and HO-1 by western blot. The results showed that the genotype of rs5746841 in 93 normal controls and 103 KBD subjects were C/C totally, but A/A and A/C were not found, which indicated preliminarily that there was no correlation between rs5746841 in TrxR2 gene and susceptibility of KBD. The expression of TrxR was lower in KBD than in normal control group significantly, while the expressions of Nrf2 and HO-1 were higher in KBD than in normal control group. These results indicated that the low expression of selenoprotein TrxR may be a candidate factor of KBD, which related to Nrf2/HO-1 signaling pathway.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Guo X, Ma W, Zhang F, Ren F, Qu C, Lammi M (2014) Recent advances in the research of an endemic osteochondropathy in China: Kashin-Beck disease. Osteoarthr Cartil 22:1774–1783

    Article  CAS  PubMed  Google Scholar 

  2. Li S, Xiao T, Zheng B (2012) Medical geology of arsenic, selenium and thallium in China. Sci Total Environ 421-422:31–40

    Article  CAS  PubMed  Google Scholar 

  3. Sun LY, Li Q, Meng FG, Fu Y, Zhao ZJ, Wang LH (2012) T-2 toxin contamination in grains and selenium concentration in drinking water and grains in Kaschin-Beck disease endemic areas of Qinghai Province. Biol Trace Elem Res 150:371–375

    Article  CAS  PubMed  Google Scholar 

  4. Ying G, Jia Y, Luan R (2007) Research advance on relation between humic acid and chondrocyte injuries. Wei Sheng Yan Jiu 36:238–241

    CAS  PubMed  Google Scholar 

  5. Brown KM, Arthur JR (2001) Selenium, selenoproteins and human health: a review. Public Health Nutr 4:593–599

    Article  CAS  PubMed  Google Scholar 

  6. Yang L, Zhao GH, Yu FF, Zhang RQ, Guo X (2016) Selenium and iodine levels in subjects with Kashin-Beck disease: a meta-analysis. Biol Trace Elem Res 170:43–54

    Article  CAS  PubMed  Google Scholar 

  7. Yu FF, Han J, Wang X, Fang H, Liu H, Guo X (2016) Salt-rich selenium for prevention and control children with Kashin-Beck disease: a meta-analysis of community-based trial. Biol Trace Elem Res 170:25–32

    Article  CAS  PubMed  Google Scholar 

  8. Zhang B, Yang L, Wang W, Li Y, Li H (2011) Environmental selenium in the Kaschin-Beck disease area, Tibetan Plateau, China. Environ Geochem Health 33:495–501

    Article  CAS  PubMed  Google Scholar 

  9. Shi XW, Guo X, Ren FL, Lu AL, Zhang YZ (2008) Familial aggregation and sibling heritability in Kashin-Beck disease. Nan Fang Yi Ke Da Xue Xue Bao 28:1187–1189

    PubMed  Google Scholar 

  10. Kryukov GV, Castellano S, Novoselov SV, Lobanov AV, Zehtab O, Guigo R et al (2003) Characterization of mammalian selenoproteomes. Science 300:1439–1443

    Article  CAS  Google Scholar 

  11. Fradejas-Villar N (2018) Consequences of mutations and inborn errors of selenoprotein biosynthesis and functions. Free Radic Biol Med 127:206–214

    Article  CAS  PubMed  Google Scholar 

  12. Wu R, Zhang R, Xiong Y, Sun W, Li Y, Yang X, Liu JF, Jiang Y, Guo H, Mo XY, Cao JL (2018) The study on polymorphisms of Sep15 and TrxR2 and the expression of AP-1 signaling pathway in Kashin-Beck disease. Bone 120:239–245

  13. Lu W, Mo XY, Xiong YM (2010) TrxR2 gene polymorphisms may not be associated with the susceptibility to Kashin-Beck disease. Nan Fang Yi Ke Da Xue Xue Bao 30:2246–2248

    CAS  PubMed  Google Scholar 

  14. Lu J, Zhong L, Lonn ME, Burk RF, Hill KE, Holmgren A (2009) Penultimate selenocysteine residue replaced by cysteine in thioredoxin reductase from selenium-deficient rat liver. FASEB J 23:2394–2402

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Zhao N, Guo FF, Xie KQ, Zeng T (2018) Targeting Nrf-2 is a promising intervention approach for the prevention of ethanol-induced liver disease. Cell Mol Life Sci 75(17):3143–3157

    Article  CAS  PubMed  Google Scholar 

  16. Liu R, Yan X (2018) Sulforaphane protects rabbit corneas against oxidative stress injury in keratoconus through activation of the Nrf-2/HO-1 antioxidant pathway. Int J Mol Med 42(5):2315–2328

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Xiaoyan Mo or Yongmin Xiong.

Ethics declarations

This study was approved by the Human Ethics Committee of Xi’an Jiaotong University.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, Y., Mo, X. & Xiong, Y. The Study on Polymorphism of TrxR and Nrf2/HO-1 Signaling Pathway in Kaschin-Beck Disease. Biol Trace Elem Res 190, 303–308 (2019). https://doi.org/10.1007/s12011-018-1566-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12011-018-1566-9

Keywords

Navigation