Preparation of Primary Cultured Dopaminergic Neurons from Mouse Brain

Author(s):  
Won-Seok Choi ◽  
Hyung-Wook Kim ◽  
Zhengui Xia
2020 ◽  
Author(s):  
Mélanie H. Thomas ◽  
Mona Karout ◽  
Beatriz Pardo Rodriguez ◽  
Yujuan Gui ◽  
Christian Jaeger ◽  
...  

AbstractMouse models have been instrumental in understanding genetic determinants of aging and its crucial role in neurodegenerative diseases. However, few studies have analyzed the evolution of the mouse brain over time at baseline. Furthermore, mouse brain studies are commonly conducted on the C57BL/6 strain, limiting the analysis to a specific genetic background. In Parkinson’s disease, the gradual demise of nigral dopaminergic neurons mainly contributes to the motor symptoms. Interestingly, a decline of the dopaminergic neuron function and integrity is also a characteristic of physiological aging in some species. Age-related nigro-striatal features have never been studied in mice of different genetic backgrounds. In this study, we analyze the morphological features in the striatum of three common mouse strains, C57BL/6J, A/J, and DBA/2J at 3-, 9- and 15 months of age. By measuring dopaminergic markers, we uncover age-related changes that differ between strains and evolve dynamically over time. Overall, our results highlight the importance of considering background strain and age when studying the murine nigro-striatal circuit in health and disease.HighlightsStudy of the integrity of the nigro-striatal circuit in C57BL/6J, A/J, and DBA/2J at different agesAge related evolution of essential features of nigral dopaminergic neurons differ between strainsConsider background strain and age is crutial to study the nigrostriatal circuit in health and disease


2006 ◽  
Vol 544 (1-3) ◽  
pp. 1-9 ◽  
Author(s):  
Lin Zhang ◽  
Yukihiko Shirayama ◽  
Eiji Shimizu ◽  
Masaomi Iyo ◽  
Kenji Hashimoto

2009 ◽  
Vol 1286 ◽  
pp. 208-214 ◽  
Author(s):  
Joo-Yong Lee ◽  
Hyo Jin Son ◽  
Ji Hyun Choi ◽  
Eunsil Cho ◽  
Jean Kim ◽  
...  

1999 ◽  
Vol 851 (1-2) ◽  
pp. 125-132 ◽  
Author(s):  
Cristina Bäckman ◽  
Thomas Perlmann ◽  
Åsa Wallén ◽  
Barry J Hoffer ◽  
Marisela Morales

1996 ◽  
Vol 93 (1-2) ◽  
pp. 136-142 ◽  
Author(s):  
Rosana Sibug ◽  
Eva Küppers ◽  
Cordian Beyer ◽  
Stephen C. Maxson ◽  
Christof Pilgrim ◽  
...  

2011 ◽  
Vol 121 (2) ◽  
pp. 715-725 ◽  
Author(s):  
Christian Hansen ◽  
Elodie Angot ◽  
Ann-Louise Bergström ◽  
Jennifer A. Steiner ◽  
Laura Pieri ◽  
...  

1989 ◽  
Vol 9 ◽  
pp. 143
Author(s):  
Sunao Furune ◽  
Kiyokuni Miura ◽  
Yukihiro Ohya ◽  
Kazuyoshi Watanabe ◽  
Shizuko Nagao ◽  
...  

2021 ◽  
Author(s):  
Benjamin D. Hobson ◽  
Se Joon Choi ◽  
Rajesh K. Soni ◽  
David Sulzer ◽  
Peter A Sims

Dopaminergic neurons modulate neural circuits and behaviors via dopamine release from expansive, long range axonal projections. The elaborate cytoarchitecture of these neurons is embedded within complex brain tissue, making it difficult to access the neuronal proteome using conventional methods. Here, we demonstrate APEX2 proximity labeling within genetically targeted neurons in the mouse brain, enabling subcellular proteomics with cell type-specificity. By combining APEX2 biotinylation with mass spectrometry, we mapped the somatodendritic and axonal proteomes of midbrain dopaminergic neurons. Our dataset reveals the proteomic architecture underlying proteostasis, axonal metabolism, and neurotransmission in these neurons. We find a significant enrichment of proteins encoded by Parkinson's disease-linked genes in striatal dopaminergic axons, including proteins with previously undescribed axonal localization. These proteomic datasets provide a resource for neuronal cell biology, and this approach can be readily adapted for study of other neural cell types.


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