Test-retest reproducibility of atomic force microscopy measurements of human trabecular meshwork stiffness

Purpose: The purpose of the present study was to quantify test-retest reproducibility of measurements of stiffness of the human trabecular meshwork (HTM) by atomic force microscopy (AFM). Methods: Eleven 40 μm radial limbal cryostat sections from a fresh human donor rim were mounted on charged slides and rehydrated at room temperature. Stiffness at four TM locations (anterior to posterior along Schlemm’s canal) was measured by AFM. At each location, a 6 x 6 grid was sampled. Indentation points were evenly distributed over a 20 μm x 20 μm area, with a rate of one load/unload cycle per second. Measurements were then repeated for calculation of test-retest variability. Results: The test-retest coefficients of variation for the four measurement locations (anterior to posterior) were 24.39, 25.28, 12.74, and 14.26%, respectively, with a notable drop in the two posterior locations compared to the anterior. The test-retest coefficient for the sections was 19.17%. For the entire eye, the test-retest coefficient of variation for the measurement of the TM stiffness was 17.13%. Young’s moduli consistently decreased from anterior to posterior location. Conclusions: Wide regional variation suggests that single value does little to fully describe the complex array of TM stiffness levels within the eye, and future studies of TM stiffness assessed by AFM should include multiple tissue samples from each eye, with documentation of the anterior-posterior location of each measurement.

[1]  M. Sassi,et al.  Toward the realization of reproducible Atomic Force Microscopy measurements of elastic modulus in biological samples. , 2015, Journal of biomechanics.

[2]  Joshua T. Morgan,et al.  The intrinsic stiffness of human trabecular meshwork cells increases with senescence , 2015, Oncotarget.

[3]  F. Yuan,et al.  Mechanical analysis of rat trabecular meshwork. , 2015, Soft matter.

[4]  Joshua T. Morgan,et al.  Wnt inhibition induces persistent increases in intrinsic stiffness of human trabecular meshwork cells. , 2015, Experimental eye research.

[5]  T. Fukuma,et al.  Significant improvements in stability and reproducibility of atomic-scale atomic force microscopy in liquid , 2014, Nanotechnology.

[6]  Pedro Gonzalez,et al.  Circumferential tensile stiffness of glaucomatous trabecular meshwork. , 2014, Investigative ophthalmology & visual science.

[7]  H. Gong,et al.  The effect of the endothelial cell cortex on atomic force microscopy measurements. , 2013, Biophysical journal.

[8]  Irene Georgakoudi,et al.  Characterization of mechanical and biochemical properties of developing embryonic tendon , 2013, Proceedings of the National Academy of Sciences.

[9]  D. Epstein,et al.  Differential effects of trabecular meshwork stiffness on outflow facility in normal human and porcine eyes. , 2012, Investigative ophthalmology & visual science.

[10]  T. Schäffer,et al.  Evaluation of lamina cribrosa and peripapillary sclera stiffness in pseudoexfoliation and normal eyes by atomic force microscopy. , 2012, Investigative ophthalmology & visual science.

[11]  Andrew R. Harris,et al.  Experimental validation of atomic force microscopy-based cell elasticity measurements , 2011, Nanotechnology.

[12]  W. Halfter,et al.  Age-dependent changes in the structure, composition and biophysical properties of a human basement membrane. , 2010, Matrix biology : journal of the International Society for Matrix Biology.

[13]  K. Yamanaka,et al.  Suppression of spurious vibration of cantilever in atomic force microscopy by enhancement of bending rigidity of cantilever chip substrate. , 2007, The Review of scientific instruments.

[14]  R. Gates,et al.  Direct measurement of cantilever spring constants and correction for cantilever irregularities using an instrumented indenter. , 2007, The Review of scientific instruments.

[15]  W. Halfter,et al.  Biomechanical properties of native basement membranes , 2007, The FEBS journal.

[16]  Holger Schönherr,et al.  Quantitative nanotribology by AFM: a novel universal calibration platform. , 2006, Langmuir : the ACS journal of surfaces and colloids.

[17]  Andreea Trache,et al.  Atomic force-multi-optical imaging integrated microscope for monitoring molecular dynamics in live cells. , 2005, Journal of biomedical optics.

[18]  M. Fresta,et al.  Atomic force microscopy and photon correlation spectroscopy: two techniques for rapid characterization of liposomes. , 2005, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[19]  S. Drance,et al.  Risk factors for progression of visual field abnormalities in normal-tension glaucoma. , 2001, American journal of ophthalmology.

[20]  J. Danias,et al.  Comparison of glaucomatous progression between untreated patients with normal-tension glaucoma and patients with therapeutically reduced intraocular pressures. The effectiveness of intraocular pressure reduction in the treatment of normal-tension glaucoma. , 1999, American journal of ophthalmology.

[21]  P. Mitchell,et al.  Prevalence of open-angle glaucoma in Australia. The Blue Mountains Eye Study. , 1996, Ophthalmology.

[22]  M. C. Leske,et al.  Risk factors for open-angle glaucoma. The Barbados Eye Study. , 1995, Archives of ophthalmology.

[23]  M. Radmacher,et al.  Imaging soft samples with the atomic force microscope: gelatin in water and propanol. , 1995, Biophysical journal.

[24]  M. C. Leske,et al.  The Barbados Eye Study. Prevalence of open angle glaucoma. , 1994, Archives of ophthalmology.

[25]  A. Elsheikh,et al.  Assessment of corneal biomechanical behavior under posterior and anterior pressure. , 2013, Journal of refractive surgery.

[26]  P. Russell,et al.  Elastic modulus determination of normal and glaucomatous human trabecular meshwork. , 2012, Investigative ophthalmology & visual science.