Direct neuronal reprogramming: Fast forward from new concepts toward therapeutic approaches

R Bocchi, G Masserdotti, M Götz - Neuron, 2022 - cell.com
Differentiated cells have long been considered fixed in their identity. However, about 20
years ago, the first direct conversion of glial cells into neurons in vitro opened the field of" …

Revisiting astrocyte to neuron conversion with lineage tracing in vivo

LL Wang, C Serrano, X Zhong, S Ma, Y Zou, CL Zhang - Cell, 2021 - cell.com
In vivo cell fate conversions have emerged as potential regeneration-based therapeutics for
injury and disease. Recent studies reported that ectopic expression or knockdown of certain …

Therapeutic potential of PTB inhibition through converting glial cells to neurons in the brain

XD Fu, WC Mobley - Annual review of neuroscience, 2023 - annualreviews.org
Cell replacement therapy represents a promising approach for treating neurodegenerative
diseases. Contrary to the common addition strategy to generate new neurons from glia by …

Repressing PTBP1 fails to convert reactive astrocytes to dopaminergic neurons in a 6-hydroxydopamine mouse model of Parkinson's disease

W Chen, Q Zheng, Q Huang, S Ma, M Li - Elife, 2022 - elifesciences.org
Lineage reprogramming of resident glial cells to dopaminergic neurons (DAns) is an
attractive prospect of the cell-replacement therapy for Parkinson's disease (PD). However, it …

NeuroD1 induces microglial apoptosis and cannot induce microglia-to-neuron cross-lineage reprogramming

Y Rao, S Du, B Yang, Y Wang, Y Li, R Li, T Zhou, X Du… - Neuron, 2021 - cell.com
The regenerative capacity of neurons is limited in the central nervous system (CNS), with
irreversible neuronal loss upon insult. In contrast, microglia exhibit extraordinary capacity for …

Neuroregenerative gene therapy to treat temporal lobe epilepsy in a rat model

J Zheng, T Li, S Qi, B Qin, J Yu, G Chen - Progress in neurobiology, 2022 - Elsevier
Temporal lobe epilepsy (TLE) is a common drug-resistant epilepsy associated with
abundant cell death in the hippocampus. Here, we develop a novel gene therapy-mediated …

PTEN knockout using retrogradely transported AAVs transiently restores locomotor abilities in both acute and chronic spinal cord injury

AN Stewart, R Kumari, WM Bailey, EP Glaser… - Experimental …, 2023 - Elsevier
Restoring function in chronic stages of spinal cord injury (SCI) has often been met with
failure or reduced efficacy when regenerative strategies are delayed past the acute or sub …

Ectopic insert-dependent neuronal expression of GFAP promoter-driven AAV constructs in adult mouse retina

N Le, H Appel, N Pannullo, T Hoang… - Frontiers in Cell and …, 2022 - frontiersin.org
Direct reprogramming of retinal Müller glia is a promising avenue for replacing
photoreceptors and retinal ganglion cells lost to retinal dystrophies. However, questions …

[HTML][HTML] Astrocyte-to-neuron reprogramming and crosstalk in the treatment of Parkinson's disease

Y Wang, Y Xia, L Kou, S Yin, X Chi, J Li, Y Sun… - Neurobiology of …, 2023 - Elsevier
Parkinson's disease (PD) is currently the fastest growing disabling neurological disorder
worldwide, with motor and non-motor symptoms being its main clinical manifestations. The …

Neuronal replenishment via hydrogel-rationed delivery of reprogramming factors

N Mahmoudi, Y Wang, N Moriarty, NY Ahmed… - ACS …, 2024 - ACS Publications
The central nervous system's limited capacity for regeneration often leads to permanent
neuronal loss following injury. Reprogramming resident reactive astrocytes into induced …