A Hydrophobic Tissue Clearing Method for Rat Brain Tissue.
Animals
Antibodies
/ metabolism
Brain
/ physiology
Calcium-Binding Proteins
/ metabolism
Cholera Toxin
/ metabolism
Dehydration
Dopaminergic Neurons
/ metabolism
Hydrophobic and Hydrophilic Interactions
Immunohistochemistry
/ methods
Mice
Microfilament Proteins
/ metabolism
Microglia
/ metabolism
Microtomy
Rats
Rats, Inbred F344
Staining and Labeling
Tyrosine 3-Monooxygenase
/ metabolism
Journal
Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252
Informations de publication
Date de publication:
23 12 2020
23 12 2020
Historique:
entrez:
11
1
2021
pubmed:
12
1
2021
medline:
27
2
2021
Statut:
epublish
Résumé
Hydrophobic tissue clearing methods are easily adjustable, fast, and low-cost procedures that allows for the study of a molecule of interest in unaltered tissue samples. Traditional immunolabeling procedures require cutting the sample into thin sections, which restricts the ability to label and examine intact structures. However, if brain tissue can remain intact during processing, structures and circuits can remain intact for the analysis. Previously established clearing methods take significant time to completely clear the tissue, and the harsh chemicals can often damage sensitive antibodies. The iDISCO method quickly and completely clears tissue, is compatible with many antibodies, and requires no special lab equipment. This technique was initially validated for the use in mice tissue, but the current protocol adapts this method to image hemispheres of control and transgenic rat brains. In addition to this, the present protocol also makes several adjustments to preexisting protocol to provide clearer images with less background staining. Antibodies for Iba-1 and tyrosine hydroxylase were validated in the HIV-1 transgenic rat and in F344/N control rats using the present hydrophobic tissue clearing method. The brain is an interwoven network, where structures work together more often than separately of one another. Analyzing the brain as a whole system as opposed to a combination of individual pieces is the greatest benefit of this whole brain clearing method.
Identifiants
pubmed: 33427244
doi: 10.3791/61821
pmc: PMC7945813
mid: NIHMS1666698
doi:
Substances chimiques
Aif1 protein, rat
0
Antibodies
0
Calcium-Binding Proteins
0
Microfilament Proteins
0
Cholera Toxin
9012-63-9
Tyrosine 3-Monooxygenase
EC 1.14.16.2
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Video-Audio Media
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NINDS NIH HHS
ID : R01 NS100624
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD043680
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH106392
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM081740
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA013137
Pays : United States
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