Reversing Parkinson’s disease by substituting dead Neurons


Parkinson’s disease is characterized by the loss of dopaminergic neurons in the substantia nigra region of the brain. There are no disease-modifying treatments available for Parkinson’s disease. Current treatment strategies prevent neuronal loss or protect vulnerable neuronal circuits.

In a new research led by Professor Xiang-Dong Fu, PhD from the department of cellular and molecular medicine at UC San Diego School of Medicine, the researchers developed an innovative and efficient one-step conversion of isolated mouse and human astrocytes to functional neurons. They achieved this by depleting the RNA-binding protein PTB.  The new strategy would be to replace the lost neurons by creating new neurons that produce dopamine. The research paper is now published in Nature.

Previously scientists tried many ways to generate neurons in the lab, using stem cells and other means, so we can study them better, as well as to use them to replace lost neurons in neurodegenerative diseases.

Fu and his team study the PTB protein (also known as PTBP1), a well-known RNA binding protein that influences gene expression in a cell. Previously professor Fu’s lab used siRNA to silence the PTB gene in fibroblasts. They also created a stable cell line that’s permanently lacking PTB which led to the discovery that mouse cells lacking PTB are transformed into neurons.

Applying this approach to the mouse brain, they demonstrated “progressive conversion of astrocytes to new neurons that innervate into and repopulate endogenous neural circuits.” The authors added that astrocytes from different brain regions are converted to different neuronal subtypes.

In mice, just a single treatment to inhibit PTB in mice converted native astrocytes into neurons that produce the neurotransmitter dopamine. As a result, the mice’s Parkinson’s disease symptoms disappeared.

The team used a chemically induced model of Parkinson’s disease in mice, in which the mice lose dopamine-producing neurons and develop symptoms similar to Parkinson’s disease, such as movement deficiencies.

Using these mice, the researchers showed conversion of midbrain astrocytes to dopaminergic neurons, which provide axons to reconstruct the nigrostriatal circuit. Notably, “re-innervation of striatum is accompanied by restoration of dopamine levels and rescue of motor deficits.”

The treatment works like this: The researchers developed a noninfectious virus that carries an antisense oligonucleotide sequence designed to specifically bind the RNA coding for PTB, thus degrading it, preventing it from being translated into a functional protein and stimulating neuron development.

Antisense oligonucleotides are a proven approach for neurodegenerative and neuromuscular diseases which forms the basis for an FDA-approved therapy for spinal muscular atrophy and several other therapies currently in clinical trials.

The researchers administered the PTB antisense oligonucleotide treatment directly to the mouse’s midbrain, which is responsible for regulating motor control and reward behaviors, and the part of the brain that typically loses dopamine-producing neurons in Parkinson’s disease. A control group of mice received mock treatment with an empty virus or an irrelevant antisense sequence.

In the treated mice, a small subset of astrocytes converted to neurons, increasing the number of neurons by approximately 30%. Dopamine levels were restored to a level comparable to that in normal mice. What’s more, the neurons grew and sent their processes into other parts of the brain. There was no change in the control mice.

By two different measures of limb movement and response, the treated mice returned to normal within three months after a single treatment and remained completely free from symptoms of Parkinson’s disease for the rest of their lives. In contrast, the control mice showed no improvement.

Next, the team plans to optimize their methods and test the approach in mouse models that mimic Parkinson’s disease through genetic changes. The technology for PTB antisense oligonucleotide treatment is now patented and ready to be developed clinically.

Reversing Parkinson’s disease by substituting dead Neurons - Medicine Innovates

About the author

Xiang-Dong Fu is Distinguished Professor of Cellular and Molecular Medicine at University of California, San Diego. Dr. Fu received his MS degree in Virology from Wuhan University, China in 1982, PhD degree in Biochemistry from Case Western Reserve University in 1988 (via the CUSBEA program), and postdoctoral training at Harvard from 1988 to 1992. Dr. Fu joined the faculty of University of California, San Diego in 1992 (Assistant Professor, 1992-1998; Associate Professor, 1998 to 2002; and Full Professor, 2002-present).

Dr. Fu was responsible for co-discovery of SR proteins, a family of RNA binding proteins involved in constitutive and alternative pre-mRNA processing. His laboratory was the first to identify a family of kinases specific for SR proteins and demonstrated that these kinases are critical for transducing external and intracellular signals to regulate alternative splicing in the nucleus. Dr. Fu’s group elucidated a series of regulatory mechanisms for splice site selection in mammalian cells and developed multiple key technologies for high throughput analysis of gene expression, mRNA isoforms, and genomic interactions. Dr. Fu’s current research is focused on integrated regulation of gene expression at transcriptional and post-transcriptional levels. Dr. Fu’s contribution to biomedical science has been recognized by selection for the Searle Scholar award (1994) and the Leukemia and Lymphoma Society Scholar award (1997) and election to AAAS Fellow (2010).



Hao Qian, Xinjiang Kang , Jing Hu, Dongyang Zhang, Zhengyu Liang, Fan Meng, Xuan Zhang, Yuanchao Xue, Roy Maimon, Steven F Dowdy , Neal K Devaraj, Zhuan Zhou, William C Mobley, Don W Cleveland, Xiang-Dong Fu. Reversing a Model of Parkinson’s Disease With in Situ Converted Nigral Neurons. Nature . 2020 Jun;582(7813):550-556. doi: 10.1038/s41586-020-2388-4.