Evidence map›Paper›PMID 26586020›Full record

ArticleScientific reports2015

Adipose-derived Stem Cell Conditioned Media Extends Survival time of a mouse model of Amyotrophic Lateral Sclerosis.

Christine V Fontanilla, Huiying Gu, Qingpeng Liu, Timothy Z Zhu, Changwei Zhou, Brian H Johnstone, Keith L March, Robert M Pascuzzi, Martin R Farlow, Yansheng Du

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

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  14. Therapeutic Potential of Adipose Stem Cells.Advances in experimental medicine and biology · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Christine V FontanillaDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN.
Huiying GuDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN.
Qingpeng LiuDepartment of Orthopedic Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, P.R.C.
Timothy Z ZhuDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN.
Changwei ZhouDepartment of Orthopedic Surgery, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, P.R.C.
Brian H JohnstoneDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Keith L MarchDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Robert M PascuzziDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN.
Martin R FarlowDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN.
Yansheng DuDepartment of Neurology, Indiana University School of Medicine, Indianapolis, IN.
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineHarbin Medical University · CNRegenerative Medicine Institute · MX

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
NCATS NIH HHS UL1 TR001108
6 · The paper itself

Abstract

Adipose stromal cells (ASC) secrete various trophic factors that assist in the protection of neurons in a variety of neuronal death models. In this study, we tested the effects of human ASC conditional medium (ASC-CM) in human amyotrophic lateral sclerosis (ALS) transgenic mouse model expressing mutant superoxide dismutase (SOD1(G93A)). Treating symptomatic SOD1(G93A) mice with ASC-CM significantly increased post-onset survival time and lifespan. Moreover, SOD1(G93A) mice given ASC-CM treatment showed high motor neuron counts, less activation of microglia and astrocytes at an early symptomatic stage in the spinal cords under immunohistochemical analysis. SOD1(G93A) mice treated with ASC-CM for 7 days showed reduced levels of phosphorylated p38 (pp38) in the spinal cord, a mitogen-activated protein kinase that is involved in both inflammation and neuronal death. Additionally, the levels of α-II spectrin in spinal cords were also inhibited in SOD1(G93A) mice treated with ASC-CM for 3 days. Interestingly, nerve growth factor (NGF), a neurotrophic factor found in ASC-CM, played a significant role in the protection of neurodegeneration inSOD1(G93A) mouse. These results indicate that ASC-CM has the potential to develop into a novel and effective therapeutic treatment for ALS.

Indexed as

Disease Models, AnimalAdipose TissueAmyotrophic Lateral SclerosisAnimalsAstrocytesBlotting, WesternCD11b AntigenCulture Media, ConditionedGlial Fibrillary Acidic ProteinHumansImmunohistochemistryMice, TransgenicMicrogliaMotor Neuronsp38 Mitogen-Activated Protein KinasesPhosphorylationCD11b AntigenCulture Media, ConditionedGlial Fibrillary Acidic Proteinp38 Mitogen-Activated Protein KinasesSOD1 G93A proteinSpectrinSuperoxide Dismutase

Identifiers

PMID26586020
PMCPMC4653659
OpenAlexW2341575018

What OpenQuestion holds

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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.