A Quantitative Evaluation of a 2.5 kb Rat Tyrosine Hydroxylase Promoter to Target Expression in Ventral Mesencephalic Dopamine Neurons In Vivo

Highlights • AAV vectors with specific promoters for neuron phenotypes are powerful tools in neuroscience, particularly in optogenetics. • Midbrain dopamine neurons have great interest because they play a central role in neurodegenerative and psychiatric disease. • To facilitate their study we analy...

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Veröffentlicht in:Neuroscience 2017-03, Vol.346, p.126-134
Hauptverfasser: Rolland, Anne-Sophie, Kareva, Tatyana, Kholodilov, Nikolai, Burke, Robert E
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container_title Neuroscience
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creator Rolland, Anne-Sophie
Kareva, Tatyana
Kholodilov, Nikolai
Burke, Robert E
description Highlights • AAV vectors with specific promoters for neuron phenotypes are powerful tools in neuroscience, particularly in optogenetics. • Midbrain dopamine neurons have great interest because they play a central role in neurodegenerative and psychiatric disease. • To facilitate their study we analyzed specificity and efficiency of a 2.5 kb sequence of rat tyrosine hydroxylase promoter. • Regional specificity was good, as no expression was seen in striatum or cortex, but cellular specificity in SN was only 50% • This promoter has utility in the study of dopaminergic neurons, but incomplete specificity necessitates caution in its use.
doi_str_mv 10.1016/j.neuroscience.2017.01.014
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects AAV
Animals
Dependovirus - physiology
dopamine
Dopaminergic Neurons - metabolism
Genetic Vectors
Immunohistochemistry
Luminescent Proteins - genetics
Luminescent Proteins - metabolism
Male
Mice, Inbred C57BL
Neurology
Optogenetics
promoter
Promoter Regions, Genetic
Rats
Red Fluorescent Protein
substantia nigra
Substantia Nigra - metabolism
Transgenes
Tyrosine 3-Monooxygenase - genetics
Tyrosine 3-Monooxygenase - metabolism
tyrosine hydroxylase
title A Quantitative Evaluation of a 2.5 kb Rat Tyrosine Hydroxylase Promoter to Target Expression in Ventral Mesencephalic Dopamine Neurons In Vivo
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