Mimura Tatsuya
Department of Ophthalmology, University of Tokyo Graduate School of Medicine, Japan.
Nippon Ganka Gakkai Zasshi. 2006 Nov;110(11):879-97.
Researchers have demonstrated the feasibility of transplanting human cultured corneal endothelial cells (HCEC) in various animal models. This review provides an overview of recent advances in our understanding of cultured corneal endothelial cell transplantation. We propose HCEC transplantation with a collagen sheet as the substitute carrier of HCEC. We also propose a novel strategy for corneal endothelial cell deficiency with the injection of adult human corneal endothelial precursors (HCEP). Using white rabbits or nude rats as keratopathy models, cultured HCEC were seeded on a collagen sheet. Descemetorhexis was performed on rabbit eyes. The HCEC collagen sheet was brought into the anterior chamber and fixed to the posterior stroma (HCEC group). Rabbit corneas with collagen sheet transplantation after descemetorhexis(collagen group) and with only descemetorhexis(no transplantation group) were the controls, respectively. As for HCEP transplantation, HCEP, isolated from rabbit corneal endothelial cells by sphere-forming assay, were injected into the anterior chamber and a face-down position was maintained for 24 hours in the rabbits (HCEP group). Pump function parameters of the HCEC sheets were 76-95% of those of human donor corneas. Mean corneal thickness in the HCEC group was significantly less than in the collagen and no transplantation groups 1, 3, 7, 14, 21, and 28 days (p< 0.05) after surgery. Cells were spread over the rear corneal surface in the HCEC group. In HE staining, marked stromal edema was present in the collagen and in the no transplantation groups, but not in the HCEC group with collagen sheets bearing monolayer cells. In the HCEP group, injected spheres were spread over the rear surface of the cornea and corneal edema was markedly suppressed. Our findings indicate that transplantation of cultured HCEC from adult human donor cornea by means of a collagen sheet can maintain the function of corneal dehydration. This suggests the feasibility of transplantation using cultured HCEC with a collagen sheet for corneal endothelial cell dysfunction. Additionally, adult precursor injection therapy can be also an effective strategy for corneal endothelial cell deficiency in place of conventional full-thickness corneal transplantation.
研究人员已在多种动物模型中证明了移植人培养角膜内皮细胞(HCEC)的可行性。本综述概述了我们对培养角膜内皮细胞移植理解的最新进展。我们提出以胶原片作为HCEC的替代载体进行HCEC移植。我们还提出了一种通过注射成人角膜内皮前体细胞(HCEP)治疗角膜内皮细胞缺乏症的新策略。以白兔或裸鼠作为角膜病变模型,将培养的HCEC接种在胶原片上。对兔眼进行后弹力层撕除术。将HCEC胶原片放入前房并固定于后基质(HCEC组)。后弹力层撕除术后进行胶原片移植的兔角膜(胶原组)和仅进行后弹力层撕除术的兔角膜(未移植组)分别作为对照。至于HCEP移植,通过成球试验从兔角膜内皮细胞中分离出的HCEP被注入前房,兔子保持俯卧位24小时(HCEP组)。HCEC片的泵功能参数为人类供体角膜的76 - 95%。术后1、3、7、14、21和28天,HCEC组的平均角膜厚度显著低于胶原组和未移植组(p<0.05)。HCEC组的细胞分布于角膜后表面。在苏木精 - 伊红染色中,胶原组和未移植组出现明显的基质水肿,而带有单层细胞的胶原片的HCEC组未出现。在HCEP组,注入的球体分布于角膜后表面,角膜水肿明显减轻。我们的研究结果表明,通过胶原片移植成人供体角膜培养的HCEC可以维持角膜脱水功能。这表明使用培养的HCEC与胶原片进行移植治疗角膜内皮细胞功能障碍具有可行性。此外,成人前体细胞注射疗法也可以作为替代传统全层角膜移植治疗角膜内皮细胞缺乏症的有效策略。