Skip to main content

Advertisement

Log in

On influence of sulfated glycosaminoglycans on tensile properties of posterior sclera

  • Original Paper
  • Published:
Mechanics of Soft Materials Aims and scope Submit manuscript

Abstract

The biomechanical behavior of sclera is conferred by the composition and structure of its extracellular matrix, which is mainly composed of collagen fibers and sulfated glycosaminoglycans (GAGs). Pathological conditions and visual disorders such as glaucoma and myopia could cause significant changes to the mechanical properties and GAG content of sclera. There exists sufficient evidence for the contribution of collagen fibers to the scleral biomechanics; however, possible mechanical roles of GAGs are not fully known. The primary objective of this work was to examine the mechanical function of GAGs through characterizing their effects on the scleral tensile response. For this purpose, chondroitinase ABC was used to deplete GAGs from posterior porcine scleral samples. Comprehensive biochemical and histological analyses were then performed to confirm and quantify GAG removal. Stress-controlled tensile tests with preconditioning were conducted in order to characterize the viscoelastic tensile behavior of treated and untreated specimens. It was found that the enzyme treatment caused a significant thickness reduction but it did not cause any significant change in the tensile properties of sclera. Overall, the findings of this study suggested that alternations in the GAG content of posterior scleral tissue are not important to tensile properties of sclera that are measured by stress-controlled experiments.

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
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Watson, P.G., Young, R.D.: Scleral structure, organisation and disease. A review. Exp. Eye Res. 78(3), 609–623 (2004)

    Article  Google Scholar 

  2. Rada, J.A.S., Shelton, S., Norton, T.T.: The sclera and myopia. Exp. Eye Res. 82(2), 185–200 (2006)

    Article  Google Scholar 

  3. Harper, A.R., Summers, J.A.: The dynamic sclera: extracellular matrix remodeling in normal ocular growth and myopia development. Exp. Eye Res. 133, 100–111 (2015)

    Article  Google Scholar 

  4. McBrien, N.A., Cornell, L.M., Gentle, A.: Structural and ultrastructural changes to the sclera in a mammalian model of high myopia. Invest. Ophthalmol. Vis. Sci. 42(10), 2179–2187 (2001)

    Google Scholar 

  5. Norton, T.T., Rada, J.A.: Reduced extracellular matrix in mammalian sclera with induced myopia. Vis. Res. 35(9), 1271–1281 (1995)

    Article  Google Scholar 

  6. Rada, J.A., Nickla, D.L., Troilo, D.: Decreased proteoglycan synthesis associated with form deprivation myopia in mature primate eyes. Invest. Ophthalmol. Vis. Sci. 41(8), 2050–2058 (2000)

    Google Scholar 

  7. Rada, J.A., Achen, V.R., Penugonda, S., Schmidt, R.W., Mount, B.A.: Proteoglycan composition in the human sclera during growth and aging. Invest. Ophthalmol. Vis. Sci. 41(7), 1639–1648 (2000)

    Google Scholar 

  8. Brown, C., Vural, M., Johnson, M., Trinkaus-Randall, V.: Age-related changes of scleral hydration and sulfated glycosaminoglycans. Mech. Ageing Dev. 77(2), 97–107 (1994)

    Article  Google Scholar 

  9. Scott, J.E., Thomlinson, A.M.: The structure of interfibrillar proteoglycan bridges (‘shape modules’) in extracellular matrix of fibrous connective tissues and their stability in various chemical environments. J. Anat. 192(Pt 3), 391–405 (1998)

  10. Lewis, P.N., Pinali, C., Young, R.D., Meek, K.M., Quantock, A.J., Knupp, C.: Structural interactions between collagen and proteoglycans are elucidated by three-dimensional electron tomography of bovine cornea. Structure (London, England : 1993). 18(2), 239–245 (2010)

  11. Hatami-Marbini, H., Pinsky, P.M.: On mechanics of connective tissue: assessing the electrostatic contribution to corneal stroma elasticity. MRS Proc. 1239, 1239-VV1203-1207 (2011)

  12. Cheng, X., Hatami-Marbini, H., Pinsky, P.M.: Modeling collagen-proteoglycan structural interactions in the human cornea, Dordrecht, 2013. Computer Models in Biomechanics, pp. 11–24. Springer Netherlands

  13. Schmidt, M.B., Mow, V.C., Chun, L.E., Eyre, D.R.: Effects of proteoglycan extraction on the tensile behavior of articular cartilage. J. Orthop. Res. 8(3), 353–363 (1990)

    Article  Google Scholar 

  14. Lujan, T.J., Underwood, C.J., Jacobs, N.T., Weiss, J.A.: Contribution of glycosaminoglycans to viscoelastic tensile behavior of human ligament. J. Appl. Physiol. 106(2), 423–431 (2009)

    Article  Google Scholar 

  15. Murienne, B.J., Chen, M.L., Quigley, H.A., Nguyen, T.D.: The contribution of glycosaminoglycans to the mechanical behaviour of the posterior human sclera. J. R. Soc. Interface. 13(119), 20160367 (2016)

    Article  Google Scholar 

  16. Murienne, B.J., Jefferys, J.L., Quigley, H.A., Nguyen, T.D.: The effects of glycosaminoglycan degradation on the mechanical behavior of the posterior porcine sclera. Acta Biomater. 12, 195–206 (2015)

    Article  Google Scholar 

  17. Norman, R.E., Flanagan, J.G., Rausch, S.M., Sigal, I.A., Tertinegg, I., Eilaghi, A., Portnoy, S., Sled, J.G., Ethier, C.R.: Dimensions of the human sclera: thickness measurement and regional changes with axial length. Exp. Eye Res. 90(2), 277–284 (2010)

    Article  Google Scholar 

  18. Boubriak, O., Urban, J., Bron, A.: Differential effects of aging on transport properties of anterior and posterior human sclera. Exp. Eye Res. 76(6), 701–713 (2003)

    Article  Google Scholar 

  19. Schultz, D.S., Lotz, J.C., Lee, S.M., Trinidad, M.L., Stewart, J.M.: Structural factors that mediate scleral stiffness. Invest. Ophthalmol. Vis. Sci. 49(10), 4232–4236 (2008)

    Article  Google Scholar 

  20. Boubriak, O., Urban, J., Akhtar, S., Meek, K., Bron, A.: The effect of hydration and matrix composition on solute diffusion in rabbit sclera. Exp. Eye Res. 71(5), 503–514 (2000)

    Article  Google Scholar 

  21. Nicoli, S., Ferrari, G., Quarta, M., Macaluso, C., Govoni, P., Dallatana, D., Santi, P.: Porcine sclera as a model of human sclera for in vitro transport experiments: histology, SEM, and comparative permeability. Mol. Vis. 15, 259 (2009)

    Google Scholar 

  22. Olsen, T.W., Sanderson, S., Feng, X., Hubbard, W.C.: Porcine sclera: thickness and surface area. Invest. Ophthalmol. Vis. Sci. 43(8), 2529–2532 (2002)

    Google Scholar 

  23. Borcherding, M.S., Blacik, L., Sittig, R., Bizzell, J.W., Breen, M., Weinstein, H.: Proteoglycans and collagen fibre organization in human corneoscleral tissue. Exp. Eye Res. 21(1), 59–70 (1975)

    Article  Google Scholar 

  24. Hatami-Marbini, H., Etebu, E.: Hydration dependent biomechanical properties of the corneal stroma. Exp. Eye Res. 116, 47–54 (2013)

  25. Hatami-Marbini, H.: Hydration dependent viscoelastic tensile behavior of cornea. Ann. Biomed. Eng. 42(8), 1740–1748 (2014)

  26. Haut, T.L., Haut, R.C.: The state of tissue hydration determines the strain-rate-sensitive stiffness of human patellar tendon. J. Biomech. 30(1), 79–81 (1997)

  27. Geraghty, B., Jones, S.W., Rama, P., Akhtar, R., Elsheikh, A.: Age-related variations in the biomechanical properties of human sclera. J. Mech. Behav. Biomed. Mater. 16, 181–191 (2012)

  28. Lujan, T.J., Underwood, C.J., Henninger, H.B., Thompson, B.M., Weiss, J.A.: Effect of dermatan sulfate glycosaminoglycans on the quasi-static material properties of the human medial collateral ligament. J. Orthop. Res. 25(7), 894–903 (2007)

    Article  Google Scholar 

  29. Fessel, G., Snedeker, J.G.: Equivalent stiffness after glycosaminoglycan depletion in tendon—an ultra-structural finite element model and corresponding experiments. J. Theor. Biol. 268(1), 77–83 (2011)

    Article  Google Scholar 

  30. Fessel, G., Snedeker, J.G.: Evidence against proteoglycan mediated collagen fibril load transmission and dynamic viscoelasticity in tendon. Matrix Biol. 28(8), 503–510 (2009)

    Article  Google Scholar 

  31. Hatami-Marbini, H., Rahimi, A.: The relation between hydration and mechanical behavior of bovine cornea in tension. J. Mech. Behav. Biomed. Mater. 36, 90–97 (2014)

  32. Elsheikh, A., Anderson, K.: Comparative study of corneal strip extensometry and inflation tests. J. R. Soc. Interface. 2(3), 177–185 (2005)

  33. Hatami-Marbini, H., Rahimi, A.: Effects of bathing solution on tensile properties of the cornea. Exp. Eye Res. 120, 103–108 (2014)

    Article  Google Scholar 

Download references

Funding

The authors would like to acknowledge the support in part by National Science Foundation: Grant No. 1636659. The imaging services were provided by the Research Resources Center – Research Histology and Tissue Imaging Core at the University of Illinois at Chicago established with the support of the Vice Chancellor of Research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hamed Hatami-Marbini.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hatami-Marbini, H., Pachenari, M. On influence of sulfated glycosaminoglycans on tensile properties of posterior sclera. Mech Soft Mater 2, 10 (2020). https://doi.org/10.1007/s42558-020-00025-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s42558-020-00025-4

Keywords

Navigation