Center for Neuroscience and Departments of Ophthalmology and Vision Science and Cell Biology and Human Anatomy, University of California Davis, Davis, CA 95616.
F.M. Kirby Neurobiology Center, Boston Children's Hospital and Harvard Medical School, Boston, MA.
eNeuro. 2018 Apr 18;5(2). doi: 10.1523/ENEURO.0035-18.2018. eCollection 2018 Mar-Apr.
The cellular environment of the CNS is non-permissive for growth and regeneration. In the retina, transplantation of stem cells has been limited by inefficient survival and integration into existing circuits. In November 2016, as part of the National Eye Institute's Audacious Goals Initiative (AGI), a diverse collection of investigators gathered for a workshop devoted to articulating the gaps in knowledge, barriers to progress, and ideas for new approaches to understanding cellular environments within the retina and how these environments may be manipulated. In doing so, the group identified the areas of (1) retinal and optic nerve glia, (2) microglia and inflammation, and the (3) extracellular matrix (ECM) and retinal vasculature as key to advancing our understanding and manipulation of the retinal microenvironments. We summarize here the findings of the workshop for the broader scientific community.
中枢神经系统的细胞环境不利于生长和再生。在视网膜中,干细胞的移植受到存活率低和难以整合到现有回路的限制。2016 年 11 月,作为国家眼科研究所大胆目标倡议(AGI)的一部分,一群不同背景的研究人员聚集在一起,参加了一个专门讨论阐明视网膜内细胞环境知识差距、进展障碍和理解这些环境并可能加以操纵的新方法的研讨会。通过这样做,该小组确定了视网膜和视神经胶质细胞、小胶质细胞和炎症以及细胞外基质(ECM)和视网膜血管系统作为推进我们对视网膜微环境的理解和操纵的关键领域。我们在此为更广泛的科学界总结研讨会的发现。