Regeneration Through in vivo Cell Fate Reprogramming for Neural Repair

被引:30
作者
Tai, Wenjiao [1 ,2 ]
Xu, Xiao-Ming [3 ,4 ]
Zhang, Chun-Li [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Hamon Ctr Regenerat Sci & Med, Dallas, TX 75390 USA
[3] Stark Neurosci Res Inst, Spinal Cord & Brain Injury Res Grp, Indianapolis, IN USA
[4] Indiana Univ Sch Med, Dept Neurol Surg, Indianapolis, IN 46202 USA
关键词
in vivo reprogramming; adult neurogenesis; traumatic brain injury (TBI); spinal cord injury (SCI); retinopathy; Alzheimer's diseases (AD); Parkinson's disease (PD); SPINAL-CORD-INJURY; MOUSE MODEL; HIPPOCAMPAL NEUROGENESIS; ADULT NEUROGENESIS; FUNCTIONAL-NEURONS; BRAIN-INJURY; GLIAL-CELLS; NG2; GLIA; DOPAMINE NEURONS; ALPHA-SYNUCLEIN;
D O I
10.3389/fncel.2020.00107
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The adult mammalian central nervous system (CNS) has very limited regenerative capacity upon neural injuries or under degenerative conditions. In recent years, however, significant progress has been made on in vivo cell fate reprogramming for neural regeneration. Resident glial cells can be reprogrammed into neuronal progenitors and mature neurons in the CNS of adult mammals. In this review article, we briefly summarize the current knowledge on innate adult neurogenesis under pathological conditions and then focus on induced neurogenesis through cell fate reprogramming. We discuss how the reprogramming process can be regulated and raise critical issues requiring careful considerations to move the field forward. With emerging evidence, we envision that fate reprogramming-based regenerative medicine will have a great potential for treating neurological conditions such as brain injury, spinal cord injury (SCI), Alzheimer's disease (AD), Parkinson's disease (PD), and retinopathy.
引用
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页数:10
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