Evidence map›Paper›PMID 25869862›Full record

ArticleNeuroImage2015

3D mapping of neuronal migration in the embryonic mouse brain with magnetic resonance microimaging.

Abby E Deans, Youssef Zaim Wadghiri, Orlando Aristizábal, Daniel H Turnbull

Abstract read
In one paragraph

Article in NeuroImage, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

4 authors at 1 institution in 1 country.

Abby E DeansSkirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Ave, New York, NY 10016, USA.
Youssef Zaim WadghiriDepartment of Radiology, New York University School of Medicine, 540 First Ave, New York, NY 10016, USA.
Orlando AristizábalSkirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Ave, New York, NY 10016, USA.
Daniel H TurnbullSkirball Institute of Biomolecular Medicine, New York University School of Medicine, 540 First Ave, New York, NY 10016, USA; Department of Radiology, New York University School of Medicine, 540 First Ave, New York, NY 10016, USA; Department of Pathology, New York University School of Medicine, 540 First Ave, New York, NY 10016, USA. Electronic address: Daniel.Turnbull@med.nyu.edu.
New York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Ultrasound and MR Imaging of Mouse Brain Development.R01NS038461 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TURNBULL, DANIEL H · 1999 to 2016
$6.5M
MRI Tracking of Stem Cell Migration During Brain InjuryR21NS066490 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI TURNBULL, DANIEL H · 2010 to 2011
$461k
NCI NIH HHS P30 CA016087NINDS NIH HHS R01 NS038461NINDS NIH HHS R01NS038461NINDS NIH HHS R21 NS066490NINDS NIH HHS R21NS066490
6 · The paper itself

Abstract

A prominent feature of the developing mammalian brain is the widespread migration of neural progenitor (NP) cells during embryogenesis. A striking example is provided by NP cells born in the ventral forebrain of mid-gestation stage mice, which subsequently migrate long distances to their final positions in the cortex and olfactory bulb. Previous studies have used two-dimensional histological methods, making it difficult to analyze three-dimensional (3D) migration patterns. Unlike histology, magnetic resonance microimaging (micro-MRI) is a non-destructive, quantitative and inherently 3D imaging method for analyzing mouse embryos. To allow mapping of migrating NP cells with micro-MRI, cells were labeled in situ in the medial (MGE) and lateral (LGE) ganglionic eminences, using targeted in utero ultrasound-guided injection of micron-sized particles of iron-oxide (MPIO). Ex vivo micro-MRI and histology were then performed 5-6days after injection, demonstrating that the MPIO had magnetically labeled the migrating NP populations, which enabled 3D visualization and automated segmentation of the labeled cells. This approach was used to analyze the distinct patterns of migration from the MGE and LGE, and to construct rostral-caudal migration maps from each progenitor region. Furthermore, abnormal migratory phenotypes were observed in Nkx2.1(-/-) embryos, most notably a significant increase in cortical neurons derived from the Nkx2.1(-/-) LGE. Taken together, these results demonstrate that MPIO labeling and micro-MRI provide an efficient and powerful approach for analyzing 3D cell migration patterns in the normal and mutant mouse embryonic brain.

Indexed as

Cell MovementAnimalsBrainFemaleImaging, Three-DimensionalMagnetic Resonance ImagingMiceMice, Inbred ICRNeuronsLateral ganglionic eminenceLGEMagnetic resonance imagingMedial ganglionic eminenceMGEMicron-sized particles of iron-oxideMPIOMRIUBMUltrasound biomicroscopy

Identifiers

PMID25869862
PMCPMC4446241
OpenAlexW1980509509

What OpenQuestion holds

Textmetadata
LicenceTDM
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.