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Human embryonic stem cell-derived neural precursor transplants in collagen scaffolds promote recovery in injured rat spinal cord
Authors:Maryam Hatami  Nargess Zare Mehrjardi  Sahar Kiani  Katayoun Hemmesi  Hossein Azizi  Abdolhossein Shahverdi  Hossein Baharvand
Institution:1. Department of Neurosurgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China;2. Department of Pharmacy, Chongqing Zhongshan Hospital, Chongqing 400013, China;3. Department of Neurosurgery, Children''s Hospital of Chongqing Medical University, Chongqing 400014, China;2. Department of Surgery, University of Toronto, Toronto, Ontario, Canada;3. Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada;1. Department of Geochemistry, Faculty of Earth Sciences, Kharazmi University, Tehran, Iran;2. United States Geological Survey, Box 25046, MS 973, Denver Federal Center, Denver, CO 80225, USA;3. Mining Department, Faculty of Engineering, University of Kurdistan, Sanandaj, Iran;4. Geological Survey of Norway (NGU), Leiv Eirikssons vei 39, 7491 Trondheim, Norway
Abstract:Background aimsSeveral studies have reported functional improvement after transplantation of in vivo-derived neural progenitor cells (NPC) into injured spinal cord. However, the potential of human embryonic stem cell-derived NPC (hESC-NPC) as a tool for cell replacement of spinal cord injury (SCI) should be considered.MethodsWe report on the generation of NPC as neural-like tubes in adherent and feeder-free hESC using a defined media supplemented with growth factors, and their transplantation in collagen scaffolds in adult rats subjected to midline lateral hemisection SCI.ResultshESC-NPC were highly expressed molecular features of NPC such as Nestin, Sox1 and Pax6. Furthermore, these cells exhibited the multipotential characteristic of differentiating into neurons and glials in vitro. Implantation of xenografted hESC-NPC into the spinal cord with collagen scaffold improved the recovery of hindlimb locomotor function and sensory responses in an adult rat model of SCI. Analysis of transplanted cells showed migration toward the spinal cord and both neural and glial differentiation in vivo.ConclusionsThese findings show that transplantation of hESC-NPC in collagen scaffolds into an injured spinal cord may provide a new approach to SCI.
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