Femtosecond Laser Cutting of Human Crystalline Lens Capsule and Decellularization for Corneal Endothelial Bioengineering

被引:1
作者
Ben Moussa, Olfa [1 ]
Parveau, Louise [1 ]
Aouimeur, Ines [1 ]
Egaud, Gregory [2 ]
Maurin, Corantin [1 ]
Fraine, Sofiane [1 ]
Urbaniak, Sebastien [1 ]
Perrache, Chantal [1 ]
He, Zhiguo [1 ]
Xxx, Sedao [3 ]
Cortez, Oliver Dorado [1 ,4 ]
Poinard, Sylvain [1 ,4 ]
Mauclair, Cyril [3 ]
Gain, Philippe [1 ,4 ]
Thuret, Gilles [1 ,4 ]
机构
[1] Jean Monnet Univ, Fac Med, Lab Biol Engn & Imaging Ophthalmol, BiiO, Hlth Innovat Campus,10 Rue Marandiere, F-42270 St Priest, France
[2] GIE Manutech USD, 18 Rue Prof Benoit Lauras, F-42000 St Etienne, France
[3] Jean Monnet Univ, Lab Hubert Curien, 18 Rue Prof Benoit Lauras, F-42000 St Etienne, France
[4] Univ Hosp, Ophthalmol Dept, Ave Albert Raimond, F-42055 St Etienne 02, France
来源
BIOENGINEERING-BASEL | 2024年 / 11卷 / 03期
关键词
corneal bioengineering; femtosecond laser; decellularization; human anterior lens capsule; viable tissue-engineered endothelial keratoplasty;
D O I
10.3390/bioengineering11030255
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The bioengineering of corneal endothelial grafts consists of seeding in vitro cultured corneal endothelial cells onto a thin, transparent, biocompatible, and sufficiently robust carrier which can withstand surgical manipulations. This is one of the most realistic alternatives to donor corneas, which are in chronic global shortage. The anterior capsule of the crystalline lens has already been identified as one of the best possible carriers, but its challenging manual preparation has limited its use. In this study, we describe a femtosecond laser cutting process of the anterior capsule of whole lenses in order to obtain capsule discs of 8 mm diameter, similar to conventional endothelial grafts. Circular marks made on the periphery of the disc indicate its orientation. Immersion in water for 3 days is sufficient to completely remove the lens epithelial cells and to enable the seeding of corneal endothelial cells, which remain viable after 27 days of culture. Therefore, this method provides a transparent, decellularized disc ready to form viable tissue engineered endothelial grafts.
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页数:14
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