Evidence map›Paper›PMID 22536416›Full record

ArticlePloS one2012

High-throughput single-cell manipulation in brain tissue.

Joseph D Steinmeyer, Mehmet Fatih Yanik

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 27% of its field
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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Joseph D SteinmeyerDepartment of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Mehmet Fatih Yanik
Massachusetts Institute of Technology · US

Funding

High-throughput single-cell-resolution genetic and pharmacological screens usingR01NS066352 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI YANIK, MEHMET FATIH · 2009 to 2012
$1.7M
NINDS NIH HHS R01 NS066352
6 · The paper itself

Abstract

The complexity of neurons and neuronal circuits in brain tissue requires the genetic manipulation, labeling, and tracking of single cells. However, current methods for manipulating cells in brain tissue are limited to either bulk techniques, lacking single-cell accuracy, or manual methods that provide single-cell accuracy but at significantly lower throughputs and repeatability. Here, we demonstrate high-throughput, efficient, reliable, and combinatorial delivery of multiple genetic vectors and reagents into targeted cells within the same tissue sample with single-cell accuracy. Our system automatically loads nanoliter-scale volumes of reagents into a micropipette from multiwell plates, targets and transfects single cells in brain tissues using a robust electroporation technique, and finally preps the micropipette by automated cleaning for repeating the transfection cycle. We demonstrate multi-colored labeling of adjacent cells, both in organotypic and acute slices, and transfection of plasmids encoding different protein isoforms into neurons within the same brain tissue for analysis of their effects on linear dendritic spine density. Our platform could also be used to rapidly deliver, both ex vivo and in vivo, a variety of genetic vectors, including optogenetic and cell-type specific agents, as well as fast-acting reagents such as labeling dyes, calcium sensors, and voltage sensors to manipulate and track neuronal circuit activity at single-cell resolution.

Indexed as

AnimalsAutomation, LaboratoryBacterial ProteinsDendritic SpinesElectroporationGene ExpressionGreen Fluorescent ProteinsGuanine Nucleotide Exchange FactorsHippocampusLuminescent ProteinsMicroscopy, FluorescenceProtein IsoformsRatsRats, Sprague-DawleyRecombinant ProteinsSingle-Cell AnalysisBacterial Proteinsenhanced green fluorescent proteinGreen Fluorescent ProteinsGuanine Nucleotide Exchange FactorsKalrn protein, ratLuminescent ProteinsProtein IsoformsRecombinant Proteinsyellow fluorescent protein, Bacteria

Identifiers

PMID22536416
PMCPMC3334978
OpenAlexW2019204301

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.