98%
921
2 minutes
20
The meso-diencephalic dopaminergic (mdDA) neurons regulate various critical processes in the mammalian nervous system, including voluntary movement and a wide range of behaviors such as mood, reward, addiction, and stress. mdDA neuronal loss is linked with one of the most prominent human movement neurological disorders, Parkinson's disease (PD). How these cells die and regenerate are two of the most hotly debated PD research topics. As for the latter, it has been long known that a series of transcription factors (TFs) involves the development of mdDA neurons, specifying cell types and controlling developmental patterns. In vitro and in vivo, TFs regulate the expression of tyrosine hydroxylase, a dopamine transporter, vesicular monoamine transporter 2, and L-aromatic amino acid decarboxylase, all of which are critical for dopamine synthesis and transport in dopaminergic neurons (DA neurons). In this review, we encapsulate the molecular mechanism of TFs underlying embryonic growth and maturation of mdDA neurons and update achievements on dopaminergic cell therapy dependent on knowledge of TFs in mdDA neuronal development. We believe that a deeper understanding of the extrinsic and intrinsic factors that influence DA neurons' fate and development in the midbrain could lead to a better strategy for PD cell therapy.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775916 | PMC |
http://dx.doi.org/10.3390/ijms23020845 | DOI Listing |
Cell Death Dis
April 2025
Swammerdam Institute for Life Sciences, Molecular Neuroscience Lab, University of Amsterdam, Amsterdam, The Netherlands.
Mesodiencephalic dopamine neurons (mdDA) of the substantia nigra pars compacta (SNc) and ventral tegmental area (VTA) play critical roles in regulating movement and motivation. Pitx3 is an essential transcription factor required for proper embryonic development and terminal differentiation of mdDA neurons. Although Pitx3 is expressed in every mdDA neuron, its ablation results only in the absence of the SNc, not the VTA.
View Article and Find Full Text PDFCold Spring Harb Protoc
April 2025
Gill Center for Biomolecular Science, Indiana University, Bloomington, Indiana 47405, USA
The nervous system of animals can sense and respond to noxious stimuli, which include noxious thermal, chemical, or mechanical stimuli, through a process called nociception. Here, we describe a simple behavioral assay to measure mechanically induced nociceptive responses in larvae. This assay tests larval mechanosensitivity to noxious force with calibrated von Frey filaments.
View Article and Find Full Text PDFInt J Mol Sci
January 2022
Center for Clinical Research on Neurological Diseases, First Affiliated Hospital, Dalian Medical University, Dalian 116021, China.
The meso-diencephalic dopaminergic (mdDA) neurons regulate various critical processes in the mammalian nervous system, including voluntary movement and a wide range of behaviors such as mood, reward, addiction, and stress. mdDA neuronal loss is linked with one of the most prominent human movement neurological disorders, Parkinson's disease (PD). How these cells die and regenerate are two of the most hotly debated PD research topics.
View Article and Find Full Text PDFInt J Mol Sci
November 2021
Swammerdam Institute for Life Sciences, University of Amsterdam, 1098 XH Amsterdam, The Netherlands.
is a member of the NK homeobox family and resembles both in homology and expression pattern. However, while is required for development of serotonergic neurons, the role of in the mid-hindbrain region is still ill-defined. We have previously shown that expression is downregulated upon loss of during development.
View Article and Find Full Text PDFCell Death Dis
October 2021
Liaoning Provincial Key Laboratory for Research on the Pathogenic Mechanisms of Neurological Diseases, the First Affiliated Hospital, Dalian Medical University, Dalian, 116011, China.
Pituitary homeobox 3 (Pitx3) is required for the terminal differentiation of nigrostriatal dopaminergic neurons during neuronal development. However, whether Pitx3 contributes to the normal physiological function and cell-type identity of adult neurons remains unknown. To explore the role of Pitx3 in maintaining mature neurons, we selectively deleted Pitx3 in the mesodiencephalic dopaminergic (mdDA) neurons of Pitx3DAT bigenic mice using a tamoxifen inducible Cre gene-targeting system.
View Article and Find Full Text PDF