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Restoration of vision after transplantation of photoreceptors

机译:感光细胞移植后视力恢复

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摘要

Cell transplantation is a potential strategy for treating blindness caused by the loss of photoreceptors. Although transplanted rod-precursor cells are able to migrate into the adult retina and differentiate to acquire the specialized morphological features of mature photoreceptor cells1, the fundamental question remains whether transplantation of photoreceptor cells can actually improve vision. Here we provide evidence of functional rod-mediated vision after photoreceptor transplantation in adult Gnatl~(-/-) mice, which lack rod function and are a model of congenital stationary night blindness. We show that transplanted rod precursors form classic triad synaptic connections with second-order bipolar and horizontal cells in the recipient retina. The newly integrated photoreceptor cells are light-responsive with dim-flash kinetics similar to adult wild-type photoreceptors. By using intrinsic imaging under scotopic conditions we demonstrate that visual signals generated by transplanted rods are projected to higher visual areas, including V1. Moreover, these cells are capable of driving optokinetic head tracking and visually guided behaviour in the Gnatl~(-/-)mouse under scotopic conditions. Together, these results demonstrate the feasibility of photoreceptor transplantation as a therapeutic strategy for restoring vision after retinal degeneration.
机译:细胞移植是治疗由光感受器丧失引起的失明的潜在策略。尽管移植的杆状前体细胞能够迁移到成年视网膜中并分化以获取成熟感光细胞的特殊形态学特征,但根本的问题仍然在于,感光细胞的移植能否真正改善视力。在这里,我们提供了成年Gnatl〜(-/-)小鼠中光感受器移植后功能杆介导的视力的证据,这些杆缺乏杆功能,是先天性静止性夜盲的模型。我们表明,移植的杆前体形成经典的三合会突触连接与受体视网膜中的二阶双极和水平细胞。与成年野生型感光细胞相似,新整合的感光细胞具有昏暗的动力学光响应。通过在暗视条件下使用固有成像,我们证明了由移植棒产生的视觉信号被投影到更高的视觉区域,包括V1。而且,这些细胞能够在暗视条件下驱动Gnatl-(-/-)小鼠的视动头部追踪和视觉引导行为。总之,这些结果证明了感光体移植作为视网膜变性后恢复视力的治疗策略的可行性。

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  • 来源
    《Nature》 |2012年第7396期|p.99-103|共5页
  • 作者单位

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Solomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Dyson Vision Research Institute, Department of Ophthalmology, Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, New York 10021, USA;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Visual Neuroscience, UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Dyson Vision Research Institute, Department of Ophthalmology, Department of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, New York 10021, USA;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Department of Visual Neuroscience, UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK;

    Solomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA;

    Developmental Biology Unit, UCL Institute of Child Health, University College London, 30 Guilford Street, London, WC1N 1 EH, UK;

    Department of Genetics UCL Institute of Ophthalmology, University College London, 11-43 Bath Street, London, EC1V 9EL, UK,Molecular Immunology Unit, UCL Institute of Child Health, University College London, 30 Guilford Street, London, WC1N 1EH, UK;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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