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Three-dimensional automated reporter quantification (3D-ARQ) technology enables quantitative screening in retinal organoids.
Vergara, M Natalia; Flores-Bellver, Miguel; Aparicio-Domingo, Silvia; McNally, Minda; Wahlin, Karl J; Saxena, Meera T; Mumm, Jeff S; Canto-Soler, M Valeria.
Afiliação
  • Vergara MN; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA natalia.vergara@ucdenver.edu valeria.canto-soler@ucdenver.edu.
  • Flores-Bellver M; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Aparicio-Domingo S; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • McNally M; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Wahlin KJ; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Saxena MT; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Mumm JS; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Canto-Soler MV; The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA natalia.vergara@ucdenver.edu valeria.canto-soler@ucdenver.edu.
Development ; 144(20): 3698-3705, 2017 10 15.
Article em En | MEDLINE | ID: mdl-28870990
ABSTRACT
The advent of stem cell-derived retinal organoids has brought forth unprecedented opportunities for developmental and physiological studies, while presenting new therapeutic promise for retinal degenerative diseases. From a translational perspective, organoid systems provide exciting new prospects for drug discovery, offering the possibility to perform compound screening in a three-dimensional (3D) human tissue context that resembles the native histoarchitecture and to some extent recapitulates cellular interactions. However, inherent variability issues and a general lack of robust quantitative technologies for analyzing organoids on a large scale pose severe limitations for their use in translational applications. To address this need, we have developed a screening platform that enables accurate quantification of fluorescent reporters in complex human iPSC-derived retinal organoids. This platform incorporates a fluorescence microplate reader that allows xyz-dimensional detection and fine-tuned wavelength selection. We have established optimal parameters for fluorescent reporter signal detection, devised methods to compensate for organoid size variability, evaluated performance and sensitivity parameters, and validated this technology for functional applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Organoides / Técnicas Genéticas / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Organoides / Técnicas Genéticas / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2017 Tipo de documento: Article