Journals / Turkish Journal of Medical Sciences / 2020 / Cilt: 50 - Sayı: 4

Roles of glycoprotein glycosylation in the pathogenesis of an endemic osteoarthritis, Kashin–Beck disease, and effectiveness evaluation of sodium hyaluronate treatment

Pages
1028–1037
Publication Date
2022-11-05
DOI
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⚡ TL;DR(Too Long; Didn't Read)

Lectin blot confirmed significant differences in HHL, AAL, and Jacalin in saliva, andHHL, PNA, PHA-E+L, and AAL in serum.Conclusion: HHL in saliva and serum may be a valuable diagnostic biomarker of KBD, and it may be used as follow-up for thehyaluronate treatment.

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Objective & Hypothesis:Background/aim: We aimed to explore the roles of glycoprotein glycosylation in the pathogenesis of Kashin–Beck disease (KBD), andevaluated the effectiveness of sodium hyaluronate treatment.Materials and methods: Blood and saliva were collected from KBD patients before and after the injection of sodium hyaluronate.
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Key Findings & Data:Increased levels ofHHL, MAL-II, and GSL-I in the untreated KBD patients discriminated them in particular from the treated ones.
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Conclusion & Impact:Lectin blot confirmed significant differences in HHL, AAL, and Jacalin in saliva, andHHL, PNA, PHA-E+L, and AAL in serum.Conclusion: HHL in saliva and serum may be a valuable diagnostic biomarker of KBD, and it may be used as follow-up for thehyaluronate treatment.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background/aim: We aimed to explore the roles of glycoprotein glycosylation in the pathogenesis of Kashin–Beck disease (KBD), andevaluated the effectiveness of sodium hyaluronate treatment.Materials and methods: Blood and saliva were collected from KBD patients before and after the injection of sodium hyaluronate. Normalhealthy subjects were included as controls. Saliva and serum lectin microarrays and saliva and serum microarray verifications were usedto screen and confirm the differences in lectin levels among the three groups.Results: In saliva lectin microarray, bindings to Sophora japonica agglutinin (SJA), Griffonia (Bandeiraea) simplicifolia lectin I (GSL-I),Euonymus europaeus lectin (EEL), Maackia amurensis lectin II (MAL-II), Sambucus nigra lectin (SNA), Hippeastrum hybrid lectin(HHL), and Aleuria aurantia lectin (AAL) were higher in the untreated KBD patients than in the control group. Increased levels ofHHL, MAL-II, and GSL-I in the untreated KBD patients discriminated them in particular from the treated ones. Jacalin was lower inthe untreated KBD patients compared to the treated KBD and control groups. In serum lectin microarray, HHL and peanut agglutinin(PNA) were increased in the untreated KBD group in comparison to the control one. AAL, Phaseolus vulgaris agglutinin (E+L) (PHAE+L), and Psophocarpus tetragonolobus lectin I (PTL-I) were lower in the untreated KBD patients compared to the treated KBD andcontrol groups. Hyaluronate treatment appeared to normalize SNA, AAL, and MAL-II levels in saliva, and HHL, PNA, AAL, PTL-I,and PHA-E+L levels in serum. Saliva reversed microarray verification confirmed significant differences between the groups in SNA andJacalin, in particular for GSL-I levels, while serum reversed microarray verification indicated that HHL, PNA, and AAL levels returnedto normal levels after the hyaluronate treatment. Lectin blot confirmed significant differences in HHL, AAL, and Jacalin in saliva, andHHL, PNA, PHA-E+L, and AAL in serum.Conclusion: HHL in saliva and serum may be a valuable diagnostic biomarker of KBD, and it may be used as follow-up for thehyaluronate treatment.

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Cite This Article

WANG, S., LIU, H., MENG, P., WU, C., LAMMI, M. J., GUO, X., GAO, Z. (2022). Roles of glycoprotein glycosylation in the pathogenesis of an endemic osteoarthritis, Kashin–Beck disease, and effectiveness evaluation of sodium hyaluronate treatment. Turkish Journal of Medical Sciences, Cilt: 50 - Sayı: 4, 1028–1037. https://ajindex.com/articles/609721

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References (12)

  1. Wang S, Guo X, Wang W, Wang S. Genome-wide study identifies the regulatory gene networks and signaling pathways from chondrocyte and peripheral blood monocyte of Kashin– Beck disease. Genes to Cells 2012
  2. 17(8): 619-632. doi: 10.1111/j.1365-2443.2012.01620.x 2. Gao Z, Guo X, Chen J, Duan C, Ma W et al. The effect of hyaluronic acid on the expression of IL-1β,TNF-α in chondrocytes of Kashin–Beck disease. Shaanxi Medical Journal 2015
  3. 44(7): 774-778. doi: 10.3969/j.issn.1000- 7377.2015.07.002 3. Gao Z, Guo X, Chen J, Duan C, Ma W et al. Effect of hyaluronic acid on collagen II and aggrecan mRNA expression in Kashin– Beck disease chondrocytes cultured in vitro. Journal of Clinical Rehabilitative Tissue Engineering Research 2009
  4. 13(46): 9061- 9065. doi:10.3969/j.issn.1673-8225.2009.46.012 4. Xia CT, Yu FF, Ren FL, Fang H, Guo X. Hyaluronic acid and glucosamine sulfate for adult Kashin–Beck disease: a clusterrandomized, placebo-controlled study. Clinical Rheumatology 2016
  5. 35(5): 1263-1270. doi: 10.1007/s10067-014-2809-6 5. Takeuchi H, Haltiwanger RS. Role of glycosylation of Notch in development. Seminars in Cell and Developmental Biology 2010
  6. 21(6): 638-645. doi: 10.1016/j.semcdb.2010.03.003 6. Manning JC, Romero A, Habermann FA, Garcia Caballero G, Kaltner H et al. Lectins: a primer for histochemists and cell biologists. Histochemistry and Cell Biology 2017
  7. 147(2): 199- 222. doi: 10.1007/s00418-016-1524-6 7. Corfield AP, Berry M. Glycan variation and evolution in the eukaryotes. Trends in Biochemical Sciences 2015
  8. 40(7): 351- 359. doi: 10.1016/j.tibs.2015.04.004 8. Pilobello KT, Slawek DE, Mahal LK. A ratiometric lectin microarray approach to analysis of the dynamic mammalian glycome. Proceedings of the National Academy of Sciences of the United States of America 2007
  9. 104(28): 11534-11539. doi: 10.1073/pnas.0704954104 9. Qin X, Guo Y, Du H, Zhong Y, Zhang J et al. Comparative analysis for glycopatterns and complex-type N-glycans of glycoprotein in sera from chronic hepatitis B- and C-infected patients. Frontiers in Physiology 2017
  10. doi: 10.3389/ fphys.2017.00596 10. Liang Y, Ma T, Thakur A, Yu H, Gao L et al. Differentially expressed glycosylated patterns of alpha-1-antitrypsin as serum biomarkers for the diagnosis of lung cancer. Glycobiology 2015
  11. 25(3): 331-340. doi: 10.1093/glycob/cwu115 11. Dwek RA. Glycobiology: towards understanding the function of sugars. Biochemical Society Transactions 1995
  12. 23(1): 1-25. doi: 10.1042/bst0230001 12.