Retinal ganglion cell repopulation for vision restoration in optic neuropathy: a roadmap from the RReSTORe Consortium

被引:0
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作者
Jonathan R. Soucy
Erika A. Aguzzi
Julie Cho
Michael James Gilhooley
Casey Keuthan
Ziming Luo
Aboozar Monavarfeshani
Meher A. Saleem
Xue-Wei Wang
Juilette Wohlschlegel
Petr Baranov
Adriana Di Polo
Brad Fortune
Kimberly K. Gokoffski
Jeffrey L. Goldberg
William Guido
Alex L. Kolodkin
Carol A. Mason
Yvonne Ou
Thomas A. Reh
Ahmara G. Ross
Brian C. Samuels
Derek Welsbie
Donald J. Zack
Thomas V. Johnson
机构
[1] Harvard Medical School,Department of Ophthalmology, Schepens Eye Research Institute of Mass. Eye and Ear
[2] University College London,The Institute of Ophthalmology
[3] Stanford University School of Medicine,Spencer Center for Vision Research, Byers Eye Institute
[4] Moorfields Eye Hospital,Department of Ophthalmology
[5] Wilmer Eye Institute,Center for Brain Science and Department of Molecular and Cellular Biology
[6] Johns Hopkins University School of Medicine,Kirby Neurobiology Center
[7] Harvard University,Department of Orthopaedic Surgery
[8] Boston Children’s Hospital,Department of Biological Structure
[9] Bascom Palmer Eye Institute,Department of Neuroscience
[10] University of Miami Health System,Discoveries in Sight Research Laboratories
[11] The Johns Hopkins University School of Medicine,Department of Ophthalmology, Roski Eye Institute
[12] University of Washington,Department of Anatomical Sciences and Neurobiology, School of Medicine
[13] University of Montreal,The Solomon H Snyder, Department of Neuroscience
[14] University of Montreal Hospital Research Centre,Departments of Pathology and Cell Biology, Neuroscience, and Ophthalmology, College of Physicians and Surgeons
[15] Devers Eye Institute and Legacy Research Institute,Department of Ophthalmology
[16] Legacy Health,Departments of Ophthalmology and Neurology
[17] University of Southern California,Department of Ophthalmology and Visual Sciences
[18] University of Louisville,Shiley Eye Institute and Viterbi Family Department of Ophthalmology
[19] Johns Hopkins University School of Medicine,Glaucoma Center of Excellence
[20] Zuckerman Mind Brain Behavior Institute,Departments of Neuroscience, Molecular Biology & Genetics, and Genetic Medicine
[21] Columbia University,Cellular & Molecular Medicine Program
[22] University of California,undefined
[23] University of Pennsylvania,undefined
[24] Callahan Eye Hospital,undefined
[25] University of Alabama at Birmingham,undefined
[26] University of California,undefined
[27] Wilmer Eye Institute,undefined
[28] Johns Hopkins University School of Medicine,undefined
[29] Johns Hopkins University School of Medicine,undefined
[30] Johns Hopkins University School of Medicine,undefined
关键词
Retinal ganglion cells; Transplantation; Neuroprotection; Organoids; Stem cells; Regenerative medicine; Ophthalmology; Glaucoma; Optic neuropathy;
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摘要
Retinal ganglion cell (RGC) death in glaucoma and other optic neuropathies results in irreversible vision loss due to the mammalian central nervous system’s limited regenerative capacity. RGC repopulation is a promising therapeutic approach to reverse vision loss from optic neuropathies if the newly introduced neurons can reestablish functional retinal and thalamic circuits. In theory, RGCs might be repopulated through the transplantation of stem cell-derived neurons or via the induction of endogenous transdifferentiation. The RGC Repopulation, Stem Cell Transplantation, and Optic Nerve Regeneration (RReSTORe) Consortium was established to address the challenges associated with the therapeutic repair of the visual pathway in optic neuropathy. In 2022, the RReSTORe Consortium initiated ongoing international collaborative discussions to advance the RGC repopulation field and has identified five critical areas of focus: (1) RGC development and differentiation, (2) Transplantation methods and models, (3) RGC survival, maturation, and host interactions, (4) Inner retinal wiring, and (5) Eye-to-brain connectivity. Here, we discuss the most pertinent questions and challenges that exist on the path to clinical translation and suggest experimental directions to propel this work going forward. Using these five subtopic discussion groups (SDGs) as a framework, we suggest multidisciplinary approaches to restore the diseased visual pathway by leveraging groundbreaking insights from developmental neuroscience, stem cell biology, molecular biology, optical imaging, animal models of optic neuropathy, immunology & immunotolerance, neuropathology & neuroprotection, materials science & biomedical engineering, and regenerative neuroscience. While significant hurdles remain, the RReSTORe Consortium’s efforts provide a comprehensive roadmap for advancing the RGC repopulation field and hold potential for transformative progress in restoring vision in patients suffering from optic neuropathies.
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