TY - JOUR
T1 - NEUROD1 Instructs Neuronal Conversion in Non-Reactive Astrocytes
AU - Brulet, Rebecca
AU - Matsuda, Taito
AU - Zhang, Ling
AU - Miranda, Carlos
AU - Giacca, Mauro
AU - Kaspar, Brian K.
AU - Nakashima, Kinichi
AU - Hsieh, Jenny
N1 - Funding Information:
We thank Woo-ping Ge, Robert Hammer, and Derek Smith for technical assistance, Chun-Li Zhang for comments on the manuscript, and Jose Cabrera and Shradha Mukherjee for graphics support. We also thank Ken McCarthy for the hGFAP-CreER mice. This work was supported by grants from the NIH (R01NS093992, R01NS089770, R01NS081203, and K02AG041815 to J.H. and T32GM083831 to R.B.), American Heart Association (15GRNT25750034 to J.H.), Department of Defense (W81XWH-15-1-0399 to J.H.), Texas Institute of Brain Injury and Repair (to J.H.), and MEXT KAKENHI (16H06527 to K.N.).
Publisher Copyright:
© 2017
PY - 2017/6/6
Y1 - 2017/6/6
N2 - Currently, all methods for converting non-neuronal cells into neurons involve injury to the brain; however, whether neuronal transdifferentiation can occur long after the period of insult remains largely unknown. Here, we use the transcription factor NEUROD1, previously shown to convert reactive glial cells to neurons in the cortex, to determine whether astrocyte-to-neuron transdifferentiation can occur under physiological conditions. We utilized adeno-associated virus 9 (AAV9), which crosses the blood-brain barrier without injury, to deliver NEUROD1 to astrocytes through an intravascular route. Interestingly, we found that a small, but significant number of non-reactive astrocytes converted to neurons in the striatum, but not the cortex. Moreover, astrocytes cultured to minimize their proliferative potential also exhibited limited neuronal transdifferentiation with NEUROD1 expression. Our results show that a single transcription factor can induce astrocyte-to-neuron conversion under physiological conditions, potentially facilitating future clinical approaches long after the acute injury phase.
AB - Currently, all methods for converting non-neuronal cells into neurons involve injury to the brain; however, whether neuronal transdifferentiation can occur long after the period of insult remains largely unknown. Here, we use the transcription factor NEUROD1, previously shown to convert reactive glial cells to neurons in the cortex, to determine whether astrocyte-to-neuron transdifferentiation can occur under physiological conditions. We utilized adeno-associated virus 9 (AAV9), which crosses the blood-brain barrier without injury, to deliver NEUROD1 to astrocytes through an intravascular route. Interestingly, we found that a small, but significant number of non-reactive astrocytes converted to neurons in the striatum, but not the cortex. Moreover, astrocytes cultured to minimize their proliferative potential also exhibited limited neuronal transdifferentiation with NEUROD1 expression. Our results show that a single transcription factor can induce astrocyte-to-neuron conversion under physiological conditions, potentially facilitating future clinical approaches long after the acute injury phase.
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U2 - 10.1016/j.stemcr.2017.04.013
DO - 10.1016/j.stemcr.2017.04.013
M3 - Article
C2 - 28506534
AN - SCOPUS:85019056323
SN - 2213-6711
VL - 8
SP - 1506
EP - 1515
JO - Stem Cell Reports
JF - Stem Cell Reports
IS - 6
ER -