Protocol for tissue clearing and 3D analysis of dopamine neurons in the developing mouse midbrain

被引:5
作者
Adolfs, Youri [1 ]
Raj, Divya D. A. [1 ]
Brignani, Sara [1 ,2 ]
Pasterkamp, R. Jeroen [1 ]
机构
[1] Univ Utrecht, Univ Med Ctr Utrecht, UMC Utrecht Brain Ctr, Dept Translat Neurosci, Univ Weg 100, NL-3584 CG Utrecht, Netherlands
[2] Max Planck Inst Neurobiol, Klopferspitz 18, D-82152 Martinsried, Germany
来源
STAR PROTOCOLS | 2021年 / 2卷 / 03期
关键词
Antibody; Microscopy; Model Organisms; Molecular Biology; Neuroscience;
D O I
10.1016/j.xpro.2021.100669
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Advances in tissue clearing enable analysis of complex migratory patterns of developing neurons in whole intact tissue. Here, we implemented a modified version of 3DISCO to study migration of midbrain dopamine (DA) neurons. We provide a detailed protocol starting from whole-brain immunostaining, tissue clearing, and ultramicroscopic imaging to post-acquisition quantification and analysis. This protocol enables precise quantification of DA neuron migration but can also be applied more generally for analyzing neuron migration throughout the nervous system.For complete details on the use and execution of this protocol, please refer to Brignani et al. (2020).
引用
收藏
页数:33
相关论文
共 8 条
  • [1] Ariel P, 2018, ULTRAMICROSCOPE 2 US, DOI [10.17615/C69M15, DOI 10.17615/C69M15]
  • [2] A Simple Method for 3D Analysis of Immunolabeled Axonal Tracts in a Transparent Nervous System
    Belle, Morgane
    Godefroy, David
    Dominici, Chloe
    Heitz-Marchaland, Celine
    Zelina, Pavol
    Hellal, Farida
    Bradke, Frank
    Chedotal, Alain
    [J]. CELL REPORTS, 2014, 9 (04): : 1191 - 1201
  • [3] Remotely Produced and Axon-Derived Netrin-1 Instructs GABAergic Neuron Migration and Dopaminergic Substantia Nigra Development
    Brignani, Sara
    Raj, Divya D. A.
    Schmidt, Ewoud R. E.
    Dudukcu, Ozge
    Adolfs, Youri
    De Ruiter, Anna A.
    Rybiczka-Tesulov, Mateja
    Verhagen, Marieke G.
    van der Meer, Christiaan
    Broekhoven, Mark H.
    Moreno-Bravo, Juan A.
    Grossouw, Laurens M.
    Dumontier, Emilie
    Cloutier, Jean-Francois
    Chedotal, Alain
    Pasterkamp, R. Jeroen
    [J]. NEURON, 2020, 107 (04) : 684 - +
  • [4] Autofluorescence spectroscopy and imaging: a tool for biomedical research and diagnosis
    Croce, A. C.
    Bottiroli, G.
    [J]. EUROPEAN JOURNAL OF HISTOCHEMISTRY, 2014, 58 (04): : 320 - 337
  • [5] STRUCTURE + ASSEMBLY OF MACROMOLECULAR LIPID COMPLEXES COMPOSED OF GLOBULAR MICELLES
    LUCY, JA
    GLAUERT, AM
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1964, 8 (05) : 727 - &
  • [6] Disentangling neural cell diversity using single-cell transcriptomics
    Poulin, Jean-Francois
    Tasic, Bosiljka
    Hjerling-Leffler, Jens
    Trimarchi, Jeffrey M.
    Awatramani, Rajeshwar
    [J]. NATURE NEUROSCIENCE, 2016, 19 (09) : 1131 - 1141
  • [7] Mapping of Brain Activity by Automated Volume Analysis of Immediate Early Genes
    Renier, Nicolas
    Adams, Eliza L.
    Kirst, Christoph
    Wu, Zhuhao
    Azevedo, Ricardo
    Kohl, Johannes
    Autry, Anita E.
    Kadiri, Lolahon
    Venkataraju, Kannan Umadevi
    Zhou, Yu
    Wang, Victoria X.
    Tang, Cheuk Y.
    Olsen, Olav
    Dulac, Catherine
    Osten, Pavel
    Tessier-Lavigne, Marc
    [J]. CELL, 2016, 165 (07) : 1789 - 1802
  • [8] STRUCTURE OF MEMBRANE HOLES IN OSMOTIC AND SAPONIN HEMOLYSIS
    SEEMAN, P
    CHENG, D
    ILES, GH
    [J]. JOURNAL OF CELL BIOLOGY, 1973, 56 (02) : 519 - 527