Evidence map›Paper›PMID 32090993›Full record

ArticleJournal of visualized experiments : JoVE2020

Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic Paraplegia.

Yongchao Mou, Sukhada Mukte, Eric Chai, Joshua Dein, Xue-Jun Li

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 17 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

5 authors at 2 institutions in 1 country.

Yongchao MouDepartment of Biomedical Sciences, University of Illinois College of Medicine Rockford; Department of Bioengineering, University of Illinois at Chicago.
Sukhada MukteDepartment of Biomedical Sciences, University of Illinois College of Medicine Rockford.
Eric ChaiDepartment of Biomedical Sciences, University of Illinois College of Medicine Rockford.
Joshua DeinMD Program, University of Illinois College of Medicine Rockford.
Xue-Jun LiDepartment of Biomedical Sciences, University of Illinois College of Medicine Rockford; Department of Bioengineering, University of Illinois at Chicago; xjli23@uic.edu.
Illinois College · USUniversity of Illinois Chicago · US

Funding

Rescuing axonal defects of human cortical neurons in hereditary spastic paraplegiasR21NS109837 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LI, XUE-JUN · 2019 to 2019
$440k
NINDS NIH HHS R21 NS109837
6 · The paper itself

Abstract

Neurons have intense demands for high energy in order to support their functions. Impaired mitochondrial transport along axons has been observed in human neurons, which may contribute to neurodegeneration in various disease states. Although it is challenging to examine mitochondrial dynamics in live human nerves, such paradigms are critical for studying the role of mitochondria in neurodegeneration. Described here is a protocol for analyzing mitochondrial transport and mitochondrial morphology in forebrain neuron axons derived from human induced pluripotent stem cells (iPSCs). The iPSCs are differentiated into telencephalic glutamatergic neurons using well-established methods. Mitochondria of the neurons are stained with MitoTracker CMXRos, and mitochondrial movement within the axons are captured using a live-cell imaging microscope equipped with an incubator for cell culture. Time-lapse images are analyzed using software with "MultiKymograph", "Bioformat importer", and "Macros" plugins. Kymographs of mitochondrial transport are generated, and average mitochondrial velocity in the anterograde and retrograde directions is read from the kymograph. Regarding mitochondrial morphology analysis, mitochondrial length, area, and aspect ratio are obtained using the ImageJ. In summary, this protocol allows characterization of mitochondrial trafficking along axons and analysis of their morphology to facilitate studies of neurodegenerative diseases.

Indexed as

AnimalsAxonsBiological TransportCells, CulturedHumansInduced Pluripotent Stem CellsMitochondriaMitochondrial DynamicsNeuronsProsencephalonSpastic Paraplegia, Hereditary

Identifiers

PMID32090993
PMCPMC7341675
OpenAlexW3004890442

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.