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Generation of Human Mesenchymal Stem Cell 3D Spheroids Using Low-binding Plates.
Redondo-Castro, Elena; Cunningham, Catriona J; Miller, Jonjo; Cain, Stuart A; Allan, Stuart M; Pinteaux, Emmanuel.
Afiliación
  • Redondo-Castro E; Division of Neuroscience and Experimental Neurology, Faculty of Biology, Medicine, and Health. University of Manchester, Manchester, UK.
  • Cunningham CJ; Division of Neuroscience and Experimental Neurology, Faculty of Biology, Medicine, and Health. University of Manchester, Manchester, UK.
  • Miller J; Division of Neuroscience and Experimental Neurology, Faculty of Biology, Medicine, and Health. University of Manchester, Manchester, UK.
  • Cain SA; Wellcome Trust Centre for Cell-Matrix Research, Division of Cell Matrix Biology & Regenerative Medicine, Faculty of Biology, Medicine, and Health, University of Manchester, Manchester, UK.
  • Allan SM; Division of Neuroscience and Experimental Neurology, Faculty of Biology, Medicine, and Health. University of Manchester, Manchester, UK.
  • Pinteaux E; Division of Neuroscience and Experimental Neurology, Faculty of Biology, Medicine, and Health. University of Manchester, Manchester, UK.
Bio Protoc ; 8(16)2018 Aug 20.
Article en En | MEDLINE | ID: mdl-30294619
The 3D culture of human mesenchymal stem cells (hMSCs) represents a more physiological environment than classical 2D culture and has been used to enhance the MSC secretome or extend cell survival after transplantation. Here we describe a simple and affordable method to generate 3D spheroids of hMSCs by seeding them at high density in a low-binding 96-well plate. Spheroids of hMSCs cultured in low-binding 96-well plates can be used to study the basic biology of the cells and to generate conditioned media or spheroids to be used in transplantation therapeutic approaches. These MSCs or their secretome can be used as a regenerative therapy and for tissue repair across multiple disease areas, including neurodegeneration. In comparison to other methods (hanging drop, use of gels or biomaterials, magnetic levitation, etc.), the method described here is simple and affordable with no need to use specialized equipment, expensive materials or complex reagents.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Bio Protoc Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Bio Protoc Año: 2018 Tipo del documento: Article Pais de publicación: Estados Unidos