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1.
Invest Ophthalmol Vis Sci ; 60(7): 2438-2448, 2019 06 03.
Artigo em Inglês | MEDLINE | ID: mdl-31158276

RESUMO

Purpose: Corneal endothelial dysfunction leads to corneal edema, pain, and vision loss. Adequate animal models are needed to study the safety and efficacy of novel cell therapies as an alternative to corneal transplantation. Methods: Primary human corneal endothelial cells (HCECs) were isolated from cadaveric donor corneas, expanded in vitro, transduced to express green fluorescent protein (GFP), loaded with superparamagnetic nanoparticles, and injected into the anterior chamber of adult rabbits immediately after endothelial cell or Descemet's membrane stripping. The same volume of balanced salt solution plus (BSS+) was injected in control eyes. We compared different models for inducing corneal edema in rabbits, and examined the ability of transplanted HCECs to reduce corneal edema over time by measuring central corneal thickness and tracking corneal clarity. GFP-positive donor cells were tracked in vivo using optical coherence tomography (OCT) fluorescence angiography module, and the transplanted cells were confirmed by human nuclei immunostaining. Results: Magnetic HCECs integrated onto the recipient corneas with intact Descemet's membrane, and donor identity was confirmed by GFP expression and immunostaining for human nuclei marker. Donor HCECs formed a monolayer on the posterior corneal surface and expressed HCEC functional markers of tight junction formation. No GFP-positive cells were observed in the trabecular meshwork or on the iris, and intraocular pressure remained stable through the length of the study. Conclusions: Our results demonstrate magnetic cell-based therapy efficiently delivers HCECs to restore corneal transparency without detectable toxicity or adverse effect on intraocular pressure. Magnetic delivery of HCECs may enhance corneal function and should be explored further for human therapies.


Assuntos
Transplante de Células/métodos , Doenças da Córnea/cirurgia , Sistemas de Liberação de Medicamentos , Endotélio Corneano/transplante , Magnetoterapia/métodos , Nanopartículas de Magnetita/química , Animais , Câmara Anterior/citologia , Sobrevivência Celular/fisiologia , Células Cultivadas , Doenças da Córnea/patologia , Portadores de Fármacos , Endotélio Corneano/metabolismo , Endotélio Corneano/cirurgia , Proteínas de Fluorescência Verde/metabolismo , Humanos , Pressão Intraocular , Substâncias Luminescentes/metabolismo , Modelos Animais , Coelhos , Doadores de Tecidos , Transfecção
2.
Curr Opin Ophthalmol ; 28(1): 35-41, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27764021

RESUMO

PURPOSE OF REVIEW: The review updates the mechanisms, clinical presentations, diagnoses, and managements of Descemet membrane detachment during cataract surgery. RECENT FINDINGS: The advent of new imaging techniques such as anterior segment optical coherence tomography and better comprehension of the clinical and pathological aspects of detachment have improved the diagnosis and treatment of this complication to the extent that the first algorithms and protocols have been proposed. SUMMARY: Though infrequent, Descemet membrane detachment is a complication of intraocular surgery, including cataract surgery and phacoemulsification. Since the first systematic description and classification in the literature by Samuels in 1928 and its characterization as a potential sight-threatening condition by Scheie in 1964, plenty of retrospective and anecdotal evidence contribute to uncertainty and debate. The main controversy still lies in the choice between conservative treatment in hopes of spontaneaous reattachment and surgical treatment in a timely manner to maximize visual recovery.


Assuntos
Extração de Catarata/efeitos adversos , Doenças da Córnea/etiologia , Lâmina Limitante Posterior/patologia , Complicações Intraoperatórias , Doenças da Córnea/diagnóstico por imagem , Doenças da Córnea/cirurgia , Humanos , Tomografia de Coerência Óptica
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