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Effect of corneal stromal lenticule customization on neurite distribution and excitatory property.
Yam, Gary Hin-Fai; Bandeira, Francisco; Liu, Yu-Chi; Devarajan, Kavya; Yusoff, Nur Zahirah Binte M; Htoon, Hla-Myint; Mehta, Jodhbir S.
Afiliação
  • Yam GH; Tissue Engineering and Cell Therapy Group, Singapore Eye Research Institute, Singapore 169856, Singapore.
  • Bandeira F; Department of Ophthalmology, University of Pittsburgh, Pittsburgh PA15213, USA.
  • Liu YC; Federal University of São Paulo, Sao Paulo, Brazil.
  • Devarajan K; São Gonçalo Eye Hospital, Rio de Janeiro, Brazil.
  • Yusoff NZBM; Tissue Engineering and Cell Therapy Group, Singapore Eye Research Institute, Singapore 169856, Singapore.
  • Htoon HM; Eye-Academic Clinical Program, Duke-National University of Singapore, Graduate Medical School, Singapore 169857, Singapore.
  • Mehta JS; Singapore Eye Research Institute, Singapore 169856, Singapore.
J Adv Res ; 38: 275-284, 2022 05.
Article em En | MEDLINE | ID: mdl-35572401
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. Objectives: 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 ß-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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cirurgia da Córnea a Laser Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cirurgia da Córnea a Laser Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article