Evidence map›Paper›PMID 25448383›Full record

ArticleJournal of neuroscience methods2015

Neurons can be labeled with unique hues by helper virus-free HSV-1 vectors expressing Brainbow.

Guo-Rong Zhang, Hua Zhao, P M Abdul Muneer, Haiyan Cao, Xu Li, Alfred I Geller

Abstract read
In one paragraph

Article in Journal of neuroscience methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. GABAPsychopharmacology · 2019
    Review
  5. Review
  6. Article
  7. CRF-amplified neuronal TLR4/MCP-1 signaling regulates alcohol self-administration.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Guo-Rong ZhangNew Jersey Neuroscience Institute, JFK Medical Center, Edison, NJ 08818, USA.
Hua ZhaoNew Jersey Neuroscience Institute, JFK Medical Center, Edison, NJ 08818, USA.
P M Abdul MuneerNew Jersey Neuroscience Institute, JFK Medical Center, Edison, NJ 08818, USA.
Haiyan CaoNew Jersey Neuroscience Institute, JFK Medical Center, Edison, NJ 08818, USA.
Xu LiNew Jersey Neuroscience Institute, JFK Medical Center, Edison, NJ 08818, USA.
Alfred I GellerNew Jersey Neuroscience Institute, JFK Medical Center, Edison, NJ 08818, USA. Electronic address: alfredgeller1@gmail.com.

Funding

Promoters for Long-term Expression from HSV-1 VectorsR01NS045855 · NINDS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GELLER, ALFRED I. · 2003 to 2011
$2.0M
Targeted gene transfer across specific synapse typesR01NS086960 · NINDS · LSU HEALTH SCIENCES CENTER · PI GELLER, ALFRED I. · 2014 to 2017
$1.4M
Targeted Gene Transfer, to Specific Types of Neurons, with HSV-1 VectorsR01NS057558 · NINDS · HARVARD MEDICAL SCHOOL · PI GELLER, ALFRED I. · 2007 to 2011
$1.3M
Correcting Cognitive Deficits by Gene TherapyK01AG025894 · NIA · HARVARD MEDICAL SCHOOL · PI ZHANG, GUORONG · 2006 to 2010
$615k
NIA NIH HHS AG025894NIA NIH HHS K01 AG025894NINDS NIH HHS NS045855NINDS NIH HHS NS057558NINDS NIH HHS NS086960NINDS NIH HHS R01 NS045855NINDS NIH HHS R01 NS057558NINDS NIH HHS R01 NS086960
6 · The paper itself

Abstract

backgroundA central problem in neuroscience is elucidating synaptic connections, the connectome. Because mammalian forebrains contain many neurons, labeling specific neurons with unique tags is desirable. A novel technology, Brainbow, creates hundreds of hues by combinatorial expression of multiple fluorescent proteins (FPs). NEW

methodWe labeled small numbers of neurons, and their axons, with unique hues, by expressing Brainbow from a helper virus-free Herpes Simplex Virus (HSV-1) vector.

resultsThe vector expresses a Brainbow cassette containing four FPs from a glutamatergic-specific promoter. Packaging HSV-Brainbow produced arrays of seven to eight Brainbow cassettes, and using Cre, each FP gene was in a position to be expressed, in different cassettes. Delivery into rat postrhinal (POR) cortex or hippocampus labeled small numbers of neurons with different, often unique, hues. An area innervated by POR cortex, perirhinal (PER) cortex, contained axons with different hues. Specific axons in PER cortex were matched to specific cell bodies in POR cortex, using hue. COMPARISON WITH EXISTING

methodsHSV-Brainbow is the only technology for labeling small numbers of neurons with unique hues. In Brainbow mice, many neurons contain the same hue. Brainbow-adeno-associated virus vectors require transduction of the same neuron with multiple vector particles, confounding neuroanatomical studies. Replication-competent Brainbow-pseudorabies virus vectors label multiple neurons with the same hue.

conclusionsAttractive properties of HSV-Brainbow include each vector particle contains multiple cassettes, representing numerous hues, recombination products are stabile, and experimental control of the number of labeled neurons. Labeling neurons with unique hues will benefit mapping forebrain circuits.

Indexed as

Genetic VectorsAnimalsAxonsBrainCell LineCricetinaeFibroblastsGene Transfer TechniquesHerpesvirus 1, HumanLuminescent ProteinsMaleNeuronsRats, Sprague-DawleyRecombination, GeneticVesicular Glutamate Transport Protein 1Luminescent ProteinsSlc17a7 protein, ratVesicular Glutamate Transport Protein 1Axon projectionBrainbowCre-mediated recombinationFluorescent proteinHerpes simplex virus vectorHue

Identifiers

PMID25448383
PMCPMC4670084

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.