Publications
425 results found
Wang R, Raykin J, Gleason RL, et al., 2015, Residual deformations in ocular tissues, JOURNAL OF THE ROYAL SOCIETY INTERFACE, Vol: 12, ISSN: 1742-5689
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- Citations: 10
Campbell IC, Coudrillier B, Mensah J, et al., 2015, Automated segmentation of the lamina cribrosa using Frangi's filter: a novel approach for rapid identification of tissue volume fraction and beam orientation in a trabeculated structure in the eye, JOURNAL OF THE ROYAL SOCIETY INTERFACE, Vol: 12, ISSN: 1742-5689
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- Citations: 33
Zhang L, Albon J, Jones H, et al., 2015, Collagen Microstructural Factors Influencing Optic Nerve Head Biomechanics, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, Vol: 56, Pages: 2031-2042, ISSN: 0146-0404
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- Citations: 68
Brady MA, Waldman SD, Ethier CR, 2015, The Application of Multiple Biophysical Cues to Engineer Functional Neocartilage for Treatment of Osteoarthritis. Part II: Signal Transduction, TISSUE ENGINEERING PART B-REVIEWS, Vol: 21, Pages: 20-33, ISSN: 1937-3368
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- Citations: 9
Brady MA, Waldman SD, Ethier CR, 2015, The Application of Multiple Biophysical Cues to Engineer Functional Neocartilage for Treatment of Osteoarthritis. Part I: Cellular Response, TISSUE ENGINEERING PART B-REVIEWS, Vol: 21, Pages: 1-19, ISSN: 1937-3368
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- Citations: 22
Coudrillier B, Geraldes D, Nghia V, et al., 2015, A novel micro-computed tomography method to measure IOP-induced deformation of the lamina cribrosa., The Annual Meeting of the Association for Research in Vision and Ophthalmology 2015
Coudrillier B, Geraldes D, Nghia V, et al., 2015, Phase-contrast micro-tomography measurements of intraocular pressure-induced deformation of the porcine lamina cribrosa, Biomechanics, Bioengineering and Biotransport Conference 2015
Braakman ST, Read AT, Chan DW-H, et al., 2015, Colocalization of outflow segmentation and pores along the inner wall of Schlemm's canal, EXPERIMENTAL EYE RESEARCH, Vol: 130, Pages: 87-96, ISSN: 0014-4835
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- Citations: 44
Stamer WD, Braakman ST, Zhou EH, et al., 2015, Biomechanics of Schlemm's canal endothelium and intraocular pressure reduction, PROGRESS IN RETINAL AND EYE RESEARCH, Vol: 44, Pages: 86-98, ISSN: 1350-9462
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- Citations: 92
Ashpole NE, Overby DR, Ethier CR, et al., 2014, Shear Stress-Triggered Nitric Oxide Release From Schlemm's Canal Cells, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, Vol: 55, Pages: 8067-8076, ISSN: 0146-0404
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- Citations: 57
Overby DR, Zhou EH, Vargas-Pinto R, et al., 2014, Altered mechanobiology of Schlemm's canal endothelial cells in glaucoma, Proceedings of the National Academy of Sciences of the United States of America, Vol: 111, Pages: 13876-13881, ISSN: 0027-8424
Increased flow resistance is responsible for the elevated intraocular pressure characteristic of glaucoma, but the cause of this resistance increase is not known. We tested the hypothesis that altered biomechanical behavior of Schlemm’s canal (SC) cells contributes to this dysfunction. We used atomic force microscopy, optical magnetic twisting cytometry, and a unique cell perfusion apparatus to examine cultured endothelial cells isolated from the inner wall of SC of healthy and glaucomatous human eyes. Here we establish the existence of a reduced tendency for pore formation in the glaucomatous SC cell—likely accounting for increased outflow resistance—that positively correlates with elevated subcortical cell stiffness, along with an enhanced sensitivity to the mechanical microenvironment including altered expression of several key genes, particularly connective tissue growth factor. Rather than being seen as a simple mechanical barrier to filtration, the endothelium of SC is seen instead as a dynamic material whose response to mechanical strain leads to pore formation and thereby modulates the resistance to aqueous humor outflow. In the glaucomatous eye, this process becomes impaired. Together, these observations support the idea of SC cell stiffness—and its biomechanical effects on pore formation—as a therapeutic target in glaucoma.
Braakman ST, Pedrigi RM, Read AT, et al., 2014, Biomechanical strain as a trigger for pore formation in Schlemm's canal endothelial cells, Experimental Eye Research, Vol: 127, Pages: 224-235, ISSN: 1096-0007
The bulk of aqueous humor passing through the conventional outflow pathway must cross the inner wall endothelium of Schlemm's canal (SC), likely through micron-sized transendothelial pores. SC pore density is reduced in glaucoma, possibly contributing to obstructed aqueous humor outflow and elevated intraocular pressure (IOP). Little is known about the mechanisms of pore formation; however, pores are often observed near dome-like cellular outpouchings known as giant vacuoles (GVs) where significant biomechanical strain acts on SC cells. We hypothesize that biomechanical strain triggers pore formation in SC cells. To test this hypothesis, primary human SC cells were isolated from three non-glaucomatous donors (aged 34, 44 and 68), and seeded on collagen-coated elastic membranes held within a membrane stretching device. Membranes were then exposed to 0%, 10% or 20% equibiaxial strain, and the cells were aldehyde-fixed 5 min after the onset of strain. Each membrane contained 3-4 separate monolayers of SC cells as replicates (N = 34 total monolayers), and pores were assessed by scanning electron microscopy in 12 randomly selected regions (∼65,000 μm2 per monolayer). Pores were identified and counted by four independent masked observers. Pore density increased with strain in all three cell lines (p < 0.010), increasing from 87 ± 36 pores/mm2 at 0% strain to 342 ± 71 at 10% strain; two of the three cell lines showed no additional increase in pore density beyond 10% strain. Transcellular “I-pores” and paracellular “B-pores” both increased with strain (p < 0.038), however B-pores represented the majority (76%) of pores. Pore diameter, in contrast, appeared unaffected by strain (p = 0.25), having a mean diameter of 0.40 μm for I-pores (N = 79 pores) and 0.67 μm for B-pores (N = 350 pores). Pore formation appears to be a mechanosensitive process that is triggered by biomechanical strain, suggesting that SC cells have th
Overby DR, Bertrand J, Tektas O-Y, et al., 2014, Ultrastructural Changes Associated With Dexamethasone-Induced Ocular Hypertension in Mice, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, Vol: 55, Pages: 4922-4933, ISSN: 0146-0404
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- Citations: 90
Amin HD, Ripolles JM, Ethier CR, et al., 2014, A novel mouse hemi-joints explant culture system for studying the response of osteochondral tissue to injury and mechanical loading, Autumn Meeting of the British-Society-for-Matrix-Biology, Publisher: WILEY-BLACKWELL, Pages: A4-A4, ISSN: 0959-9673
Campbell IC, Coudrillier B, Abel RL, et al., 2014, Effects of Lamina Cribrosa Microarchitecture on Biomechanics in Glaucoma, Publisher: ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ISSN: 0146-0404
Raykin J, Best L, Gleason R, et al., 2014, Optic Nerve Sheath Mechanics and Permeability in VIIP Syndrome, Publisher: ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ISSN: 0146-0404
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- Citations: 2
Coudrillier B, Abel RL, Albon J, et al., 2014, Micro-computed Tomography (μCT) for the Structural Analysis of the Lamina Cribrosa (LC), Publisher: ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ISSN: 0146-0404
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- Citations: 1
Overby DR, Vahabikashi A, Vargas-Pinto R, et al., 2014, The Effect of Cell Stiffness on I- and B-Pore Formation in Schlemm's Canal Endothelial Cells, Publisher: ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ISSN: 0146-0404
Chang JYH, Ethier CR, Stamer WD, et al., 2014, Differential effects of nitric oxide synthase inhibitors on conventional outflow facility in mice, Publisher: ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ISSN: 0146-0404
Ethier CR, Campbell IC, Coudrillier B, et al., 2014, Automated detection of Lamina Cribrosa (LC) beam microarchitecture from imaging data using a Frangi filter, Publisher: ASSOC RESEARCH VISION OPHTHALMOLOGY INC, ISSN: 0146-0404
Amin HD, Brady MA, St-Pierre J-P, et al., 2014, Stimulation of chondrogenic differentiation of adult human bone marrow-derived stromal cells by a moderate-strength static magnetic field, Tissue Engineering: Parts A, B, and C, Vol: 20, Pages: 1612-1620, ISSN: 1937-3368
Tissue-engineering strategies for the treatment of osteoarthritis would benefit from the ability to induce chondrogenesis in precursor cells. One such cell source is bone marrow-derived stromal cells (BMSCs). Here, we examined the effects of moderate-strength static magnetic fields (SMFs) on chondrogenic differentiation in human BMSCs in vitro. Cells were cultured in pellet form and exposed to several strengths of SMFs for various durations. mRNA transcript levels of the early chondrogenic transcription factor SOX9 and the late marker genes ACAN and COL2A1 were determined by reverse transcription–polymerase chain reaction, and production of the cartilage-specific macromolecules sGAG, collage type 2 (Col2), and proteoglycans was determined both biochemically and histologically. The role of the transforming growth factor (TGF)-β signaling pathway was also examined. Results showed that a 0.4 T magnetic field applied for 14 days elicited a strong chondrogenic differentiation response in cultured BMSCs, so long as TGF-β3 was also present, that is, a synergistic response of a SMF and TGF-β3 on BMSC chondrogenic differentiation was observed. Further, SMF alone caused TGF-β secretion in culture, and the effects of SMF could be abrogated by the TGF-β receptor blocker SB-431542. These data show that moderate-strength magnetic fields can induce chondrogenesis in BMSCs through a TGF-β-dependent pathway. This finding has potentially important applications in cartilage tissue-engineering strategies.
Brady MA, Vaze R, Amin HD, et al., 2014, The Design and Development of a High-Throughput Magneto-Mechanostimulation Device for Cartilage Tissue Engineering, TISSUE ENGINEERING PART C-METHODS, Vol: 20, Pages: 149-159, ISSN: 1937-3384
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- Citations: 8
Campbell IC, Coudrillier B, Ethier CR, 2014, Biomechanics of the Posterior Eye: A Critical Role in Health and Disease, JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, Vol: 136, ISSN: 0148-0731
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- Citations: 77
Girard MJA, Strouthidis NG, Desjardins A, et al., 2013, <i>In vivo</i> optic nerve head biomechanics: performance testing of a three-dimensional tracking algorithm, JOURNAL OF THE ROYAL SOCIETY INTERFACE, Vol: 10, ISSN: 1742-5689
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- Citations: 51
Amin HD, Brady MA, St-Pierre J-P, et al., 2013, STIMULATION OF CHONDROGENIC DIFFERENTIATION OF ADULT HUMAN PRECURSOR CELLS USING STATIC MAGNETIC FIELD AS A PHYSICAL CUE, World Congress of the Osteoarthritis-Research-Society-International (OARSI), Publisher: ELSEVIER SCI LTD, Pages: S118-S118, ISSN: 1063-4584
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- Citations: 1
Vargas-Pinto R, Pedrigi RM, Braakman S, et al., 2013, Cultured glaucomatous Schlemm's canal cells show increased subcortical stiffness and decreased pore density., MOLECULAR BIOLOGY OF THE CELL, Vol: 24, ISSN: 1059-1524
Van Doormaal MA, Kazakidi A, Wylezinska M, et al., 2012, Haemodynamics in the mouse aortic arch computed from MRI-derived velocities at the aortic root, JOURNAL OF THE ROYAL SOCIETY INTERFACE, Vol: 9, Pages: 2834-2844, ISSN: 1742-5689
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- Citations: 30
Boussommier-Calleja A, Bertrand J, Woodward DF, et al., 2012, Pharmacologic Manipulation of Conventional Outflow Facility in Ex Vivo Mouse Eyes, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, Vol: 53, Pages: 5838-5845, ISSN: 0146-0404
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- Citations: 66
Gouget CLM, Girard MJ, Ethier CR, 2012, A constrained von Mises distribution to describe fiber organization in thin soft tissues, BIOMECHANICS AND MODELING IN MECHANOBIOLOGY, Vol: 11, Pages: 475-482, ISSN: 1617-7959
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- Citations: 23
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