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Cited by 416

The DOI matches its Crossref record; 69 of the 69 references it cites were found in a registry or an index.

In vivo conversion of astrocytes to neurons in the injured adult spinal cord

Open access
Su, Zhida, Niu, Wenze, Liu, Meng-Lu, Zou, Yuhua, Zhang, Chun-Li·2014·Nature Communications

Abstract

Spinal cord injury (SCI) leads to irreversible neuronal loss and glial scar formation, which ultimately result in persistent neurological dysfunction. Cellular regeneration could be an ideal approach to replenish the lost cells and repair the damage. However, the adult spinal cord has limited ability to produce new neurons. Here we show that resident astrocytes can be converted to doublecortin (DCX)-positive neuroblasts by a single transcription factor, SOX2, in the injured adult spinal cord. Importantly, these induced neuroblasts can mature into synapse-forming neurons in vivo. Neuronal maturation is further promoted by treatment with a histone deacetylase inhibitor, valproic acid (VPA). The results of this study indicate that in situ reprogramming of endogenous astrocytes to neurons might be a potential strategy for cellular regeneration after SCI. Expression of the transcription factor SOX2 reprogrammes astrocytes into neuroblasts in the adult mouse striatum. Here, the authors use the same approach in the injured adult mouse spinal cord to convert resident astrocytes into neuroblasts that can mature into synapse-forming neurons.

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Metadata

Authors
Su, Z., Niu, W., Liu, M.-L., Zou, Y., & Zhang, C.-L.
Venue
Nature Communications
Published
2014-02-25
Volume
5
Issue
1
Pages
3338-3338
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2074131381
Cited by
416
References
69
FWCI
13.27
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: In vivo conversion of astrocytes to neurons in the injured adult spinal cord. https://app.cochat.ai/papers/10.1038/ncomms4338
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Su, Z., Niu, W., Liu, M.-L., Zou, Y., & Zhang, C.-L. (2014). In vivo conversion of astrocytes to neurons in the injured adult spinal cord. Nature Communications. https://doi.org/10.1038/ncomms4338

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