脊髓损伤修复
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Nature子刊:同济大学朱融融/程黎明团队构建新型脊髓类器官,可修复脊髓损伤并恢复运动能力
生物世界· 2025-10-27 04:23
Core Insights - The article discusses the development of engineered thoracic spinal cord organoids (enTsOrg) for potential therapeutic applications in spinal cord injury (SCI) repair, showcasing their ability to restore motor function in paralyzed mice [2][3][11] Group 1: Research Findings - The research team successfully constructed enTsOrg that mimics the heterogeneity and mature neural circuit structure of the thoracic spinal cord, leading to the reorganization of neural circuits and recovery of hind limb motor function in mice with complete spinal cord injury [3][10] - The study highlights the complexity of the central nervous system's development and opens potential pathways for designing organoids tailored for specific anatomical regions in neural injury treatment [4][11] Group 2: Methodology - The engineered organoids were created using induced pluripotent stem cells (iPSCs) derived from fibroblasts and layered double hydroxide (LDH) matrices within a basement membrane hydrogel, successfully reproducing the diverse neuronal distribution and electrophysiological characteristics similar to natural spinal cord tissue [7][9] - The transplantation of enTsOrg into a mouse model of thoracic complete spinal cord injury resulted in significant improvements in motor function, neuronal subtype diversity, and electrophysiological conduction of motor neurons compared to non-segment-specific spinal cord organoids [9][10] Group 3: Mechanisms of Action - LDH promotes the formation of region-specific thoracic spinal cord organoids by activating PTCH1 protein and regulating retinoic acid signaling pathways, enhancing neuronal survival and promoting the differentiation and maturation of motor neurons and interneurons [9][10] - The study indicates that the transplanted enTsOrg formed more refined functional neurons with dorsal and ventral characteristics, crucial for muscle contraction and extension in paralyzed animals [9][10]
心智观察所:独家对话|朱融融:脊髓损伤修复,让我深感科技造福人类的力量
Guan Cha Zhe Wang· 2025-07-05 01:41
Core Insights - The article highlights a breakthrough in spinal cord injury treatment through the development of an injectable neural system biomaterial scaffold by Dr. Zhu Rongrong and her team, which offers hope to millions of patients worldwide [1][3]. Group 1: Technology Overview - The injectable biomaterial promotes nerve regeneration and induces directional axon growth, effectively creating a neural relay station to reconnect severed spinal cord pathways [3][5]. - The material has shown significant efficacy in animal trials, particularly in improving locomotion in rodents and non-human primates [6][7]. Group 2: Clinical Implications - Annually, there are approximately 80,000 to 100,000 new cases of spinal cord injuries in China, with over 3 million patients currently affected, of which 82.5% suffer from substantial spinal cord damage without effective treatment options [7][8]. - The traditional treatment methods involve surgical debridement, which often lacks suitable materials for spinal cord repair, highlighting the need for innovative solutions like the developed biomaterial [7][8]. Group 3: Research Journey - Dr. Zhu's shift to spinal cord injury research began in 2016, focusing on utilizing biomaterials for nerve regeneration, which involves a complex interplay of material design and understanding the pathological microenvironment [4][5]. - The research team faced challenges in translating efficacy from rodent models to non-human primates, with initial trials showing no improvement until a significant breakthrough was observed after four months [6][7]. Group 4: Patient Impact - The quality of life for spinal cord injury patients is severely compromised, with many unable to perform basic tasks, emphasizing the potential transformative impact of the new biomaterial if successful in clinical applications [9][10]. - The ultimate goal of the research is to enable patients to regain mobility and independence, significantly improving their overall well-being [10].