Summary: Researchers have made a surprise discovery that could help provide treatment options for a range of conditions from Parkinson’s disease to depression. Researching how to transform supportive brain cells into neurons, the scientists unexpectedly transformed mature inhibitory striatal neurons into dopamine producing neurons.
Source: UT Southwestern Medical Center.
UT Southwestern researchers attempting to transform supporting brain cells into neurons instead reprogrammed mature inhibitory neurons into a different type of neuron that creates the neurotransmitter lost in Parkinson’s disease.
The study, published today in Stem Cell Reports, reveals the possibility of changing mature neurons from one kind to another without relying on stem cells, contrary to the prevailing view.
The mouse study indicates that the brain’s neurons are more changeable in adulthood than previously thought, said corresponding author Dr. Chun-Li Zhang, Professor of Molecular Biology at UT Southwestern Medical Center. The long-held belief was that a neuron’s identity was sealed well before adulthood and that one kind of neuron could not morph into another variety, he added.
“To find that we could manipulate neurons to change their identity in adulthood was truly unexpected,” said Dr. Zhang, a W.W. Caruth, Jr. Scholar in Biomedical Research, adding that insights into neuronal plasticity and cell identity maintenance may someday lead to therapeutic strategies for treating neurological diseases through reprogramming of local neurons.
“Initially, I was a little disappointed that we altered the properties of medium spiny neurons and not the supporting glial cells we were targeting,” he said. “But when we realized the novelty of our results, we were amazed. To our knowledge, changing the identity of resident and mature neurons had never been accomplished.”
Because the neurotransmitter dopamine is lost in movement disorders like Parkinson’s disease, many neuroscientists are interested in the possibility of someday creating new dopamine-producing neurons. Dopaminergic cells are important for controlling voluntary movement and emotions such as motivation and reward that drive behavior, he explained.
For proper function, levels of the neurotransmitters GABA, dopamine, and others need to exist in a delicate balance in the brain, he said. Because dopamine is involved in reward behavior, including addictive behaviors, any potential treatment to increase dopamine levels would also need a way to keep the levels of other neurotransmitters in balance, he added.
The mature medium spiny neurons that changed their identities in this study usually produce GABA, an inhibitory neurotransmitter that targets other neurons throughout the adult brain, Dr. Zhang explained.
Dr. Zhang and his team used a viral vector – a tool commonly used by molecular biologists to deliver genetic material into cells – to administer a cocktail of genes expected to encourage reprogramming to live mouse brains in an attempt to induce the glia to change into dopamine-producing neurons. Glia – from the Greek word for “glue” – are cells that encircle neurons to provide support, insulation, and protection.
The cocktail was injected into the striatum, a region of the brain rich in GABA-producing medium spiny neurons known to help control motor skills. Dopamine-producing neurons are normally located elsewhere in the brain but send long connections to control the medium spiny neurons in the striatum, Dr. Zhang said.
The researchers initially saw new dopamine neurons and thought the glia had converted. However, many rounds of cell lineage testing revealed that the glia remained unchanged.
“We got the new cells we wanted,” Dr. Zhang said. “But, they did not originate from glial cells.”
The unexpected results led to intense follow-up experiments that confirmed the team’s suspicion that the new cells were directly transformed from mature GABA neurons. The new cells were more like dopamine-containing neurons, despite retaining some traits of the original cells, he said, adding that characterizing the cells and their genetics in more detail is the laboratory’s current goal.
“Rather than originating from glia, the new dopamine cells came from local, existing mature neurons without passing through a stem cell state,” Dr. Zhang said. “This is a mature cell-to-mature cell transformation.”
The three lead authors include postdoctoral researcher Dr. Lei-Lei Wang and two former UTSW instructors, Dr. Wenze Niu and Dr. Tong Zang. Yuhua Zou, a research scientist in Molecular Biology, also participated in the study.
Funding: The study received support from The Welch Foundation, UTSW’s Mobility Foundation Center for Rehabilitation Research, The Michael J. Fox Foundation, the Decherd Foundation, the Judith and Jean Pape Adams Foundation, the Texas Institute for Brain Injury and Repair, the Kent Waldrep Foundation Center for Basic Research on Nerve Growth and Regeneration, and the National Institutes of Health.
Source: Deborah Wormser – UT Southwestern Medical Center
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is credited to UT Southwestern.
Original Research: Open access research for “Phenotypic Reprogramming of Striatal Neurons into Dopaminergic Neuron-like Cells in the Adult Mouse Brain” by Wenze Niu, Tong Zang,
Lei-Lei Wang, Yuhua Zou, and Chun-Li Zhang in Stem Cell Reports. Published October 11 2018.
Phenotypic Reprogramming of Striatal Neurons into Dopaminergic Neuron-like Cells in the Adult Mouse Brain
Neuronal subtype is largely fixed in the adult mammalian brain. Here, however, we unexpectedly reveal that adult mouse striatal neurons can be reprogrammed into dopaminergic neuron-like cells (iDALs). This in vivo phenotypic reprogramming can be promoted by a stem cell factor (SOX2), three dopaminergic neuron-enriched transcription regulators (NURR1, LMX1A, and FOXA2), and a chemical compound (valproic acid). Although the site of action of the reprogramming factors remains to be determined, immunohistochemistry and genetic lineage mappings confirm striatal neurons as the cell origin for iDALs. iDALs exhibit electrophysiological properties stereotypical to endogenous dopaminergic rather than striatal neurons. Together, these results indicate that neuronal phenotype can be reengineered even in the adult brain, implicating a therapeutic strategy for neurological diseases.