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https://doi.org/10.1016/j.jare.2021.09.004
Title: | Effect of corneal stromal lenticule customization on neurite distribution and excitatory property | Authors: | Yam, G.H.-F. Bandeira, F. Liu Yu-Chi Devarajan, K. Yusoff, N.Z.B.M. HLA MYINT HTOON Mehta Jodhbir Singh |
Keywords: | Corneal refractive surgery Customization Excitatory response Neurite profile SMILE Stromal lenticules |
Issue Date: | 1-Sep-2021 | Publisher: | Elsevier B.V. | Citation: | Yam, G.H.-F., Bandeira, F., Liu Yu-Chi, Devarajan, K., Yusoff, N.Z.B.M., HLA MYINT HTOON, Mehta Jodhbir Singh (2021-09-01). Effect of corneal stromal lenticule customization on neurite distribution and excitatory property. Journal of Advanced Research. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jare.2021.09.004 | Rights: | Attribution-NonCommercial-NoDerivatives 4.0 International | Abstract: | Introduction: Refractive stromal lenticules from Small Incision Lenticule Extraction (SMILE), though usually discarded, hold a potential for various ophthalmic applications, including refractive correction, stromal volume expansion, and biomechanical strengthening of the cornea. Purpose: To investigate the effect of lenticule customization on lenticule neurite length profile and the excitatory response (calcium signaling) and the potential of reinnervation. Methods: Human and porcine stromal lenticules were treated by (1) excimer laser reshaping, (2) ultraviolet A-riboflavin crosslinking (CXL), and (3) decellularization by sodium dodecyl sulfate (SDS), respectively. The overall neurite scaffold immuno-positive to TuJ1 (neuron-specific class III ?-tubulin) expression and population of active neurite fragments with calcium response revealed by L-glutamate-induced Fluo-4-acetoxymethyl ester reaction were captured by wide-field laser-scanning confocal microscopy, followed by z-stack image construction. The NeuronJ plugin was used to measure neurite lengths for TuJ1 (NL-TuJ1) and calcium signal (NL-Ca). Reinnervation of lenticules was examined by the ex vivo grafting of chick dorsal root ganglia (DRG) to the decellularized human lenticules. Differences between groups and controls were analyzed with ANOVA and Mann-Whitney U test. Results: The customization methods significantly eliminated neurites inside the lenticules. NL-TuJ1 was significantly reduced by 84% after excimer laser reshaping, 54% after CXL, and 96% after decellularization. The neurite remnants from reshaping and CXL exhibited calcium signaling, indicative of residual excitatory response. Re-innervation occurred in the decellularized lenticules upon stimulation of the grafted chick embryo DRG with nerve growth factor (NGF 2.5S). Conclusion: All of the lenticule customization procedures reduced lenticule neurites, but the residual neurites still showed excitatory potential. Even though these neurite remnants seemed minimal, they could be advantageous to reinnervation with axon growth and guidance after lenticule reimplantation for refractive and volume restoration of the cornea. © 2021 | Source Title: | Journal of Advanced Research | URI: | https://scholarbank.nus.edu.sg/handle/10635/233254 | ISSN: | 2090-1232 | DOI: | 10.1016/j.jare.2021.09.004 | Rights: | Attribution-NonCommercial-NoDerivatives 4.0 International |
Appears in Collections: | Elements Staff Publications |
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