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Article: A core scientific problem in the treatment of central nervous system diseases: Newborn neurons

TitleA core scientific problem in the treatment of central nervous system diseases: Newborn neurons
Authors
Keywordsbioactive materials
brain trauma
endogenous neurogenesis
hippocampal dentate gyrus
neural stem cells
neurotrophic factors
newborn neurons
spinal cord injury
stroke
subventricular zone
Issue Date1-Dec-2024
PublisherMedknow Publications
Citation
Neural Regeneration Research, 2024, v. 19, n. 12, p. 2588-2601 How to Cite?
AbstractIt has long been asserted that failure to recover from central nervous system diseases is due to the system's intricate structure and the regenerative incapacity of adult neurons. Yet over recent decades, numerous studies have established that endogenous neurogenesis occurs in the adult central nervous system, including humans'. This has challenged the long-held scientific consensus that the number of adult neurons remains constant, and that new central nervous system neurons cannot be created or renewed. Herein, we present a comprehensive overview of the alterations and regulatory mechanisms of endogenous neurogenesis following central nervous system injury, and describe novel treatment strategies that target endogenous neurogenesis and newborn neurons in the treatment of central nervous system injury. Central nervous system injury frequently results in alterations of endogenous neurogenesis, encompassing the activation, proliferation, ectopic migration, differentiation, and functional integration of endogenous neural stem cells. Because of the unfavorable local microenvironment, most activated neural stem cells differentiate into glial cells rather than neurons. Consequently, the injury-induced endogenous neurogenesis response is inadequate for repairing impaired neural function. Scientists have attempted to enhance endogenous neurogenesis using various strategies, including using neurotrophic factors, bioactive materials, and cell reprogramming techniques. Used alone or in combination, these therapeutic strategies can promote targeted migration of neural stem cells to an injured area, ensure their survival and differentiation into mature functional neurons, and facilitate their integration into the neural circuit. Thus can integration replenish lost neurons after central nervous system injury, by improving the local microenvironment. By regulating each phase of endogenous neurogenesis, endogenous neural stem cells can be harnessed to promote effective regeneration of newborn neurons. This offers a novel approach for treating central nervous system injury.
Persistent Identifierhttp://hdl.handle.net/10722/368445
ISSN
2023 Impact Factor: 5.9
2023 SCImago Journal Rankings: 0.967

 

DC FieldValueLanguage
dc.contributor.authorHao, Peng-
dc.contributor.authorYang, Zhaoyang-
dc.contributor.authorSo, Kwok Fai-
dc.contributor.authorLi, Xiaoguang-
dc.date.accessioned2026-01-08T00:35:16Z-
dc.date.available2026-01-08T00:35:16Z-
dc.date.issued2024-12-01-
dc.identifier.citationNeural Regeneration Research, 2024, v. 19, n. 12, p. 2588-2601-
dc.identifier.issn1673-5374-
dc.identifier.urihttp://hdl.handle.net/10722/368445-
dc.description.abstractIt has long been asserted that failure to recover from central nervous system diseases is due to the system's intricate structure and the regenerative incapacity of adult neurons. Yet over recent decades, numerous studies have established that endogenous neurogenesis occurs in the adult central nervous system, including humans'. This has challenged the long-held scientific consensus that the number of adult neurons remains constant, and that new central nervous system neurons cannot be created or renewed. Herein, we present a comprehensive overview of the alterations and regulatory mechanisms of endogenous neurogenesis following central nervous system injury, and describe novel treatment strategies that target endogenous neurogenesis and newborn neurons in the treatment of central nervous system injury. Central nervous system injury frequently results in alterations of endogenous neurogenesis, encompassing the activation, proliferation, ectopic migration, differentiation, and functional integration of endogenous neural stem cells. Because of the unfavorable local microenvironment, most activated neural stem cells differentiate into glial cells rather than neurons. Consequently, the injury-induced endogenous neurogenesis response is inadequate for repairing impaired neural function. Scientists have attempted to enhance endogenous neurogenesis using various strategies, including using neurotrophic factors, bioactive materials, and cell reprogramming techniques. Used alone or in combination, these therapeutic strategies can promote targeted migration of neural stem cells to an injured area, ensure their survival and differentiation into mature functional neurons, and facilitate their integration into the neural circuit. Thus can integration replenish lost neurons after central nervous system injury, by improving the local microenvironment. By regulating each phase of endogenous neurogenesis, endogenous neural stem cells can be harnessed to promote effective regeneration of newborn neurons. This offers a novel approach for treating central nervous system injury.-
dc.languageeng-
dc.publisherMedknow Publications-
dc.relation.ispartofNeural Regeneration Research-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectbioactive materials-
dc.subjectbrain trauma-
dc.subjectendogenous neurogenesis-
dc.subjecthippocampal dentate gyrus-
dc.subjectneural stem cells-
dc.subjectneurotrophic factors-
dc.subjectnewborn neurons-
dc.subjectspinal cord injury-
dc.subjectstroke-
dc.subjectsubventricular zone-
dc.titleA core scientific problem in the treatment of central nervous system diseases: Newborn neurons-
dc.typeArticle-
dc.identifier.doi10.4103/NRR.NRR-D-23-01775-
dc.identifier.scopuseid_2-s2.0-85190378012-
dc.identifier.volume19-
dc.identifier.issue12-
dc.identifier.spage2588-
dc.identifier.epage2601-
dc.identifier.eissn1876-7958-
dc.identifier.issnl1673-5374-

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