Evidence map›Paper›PMID 29858777›Full record

ArticleMolecular neurobiology2019

Cerebrospinal Fluid from Patients with Sporadic Amyotrophic Lateral Sclerosis Induces Degeneration of Motor Neurons Derived from Human Embryonic Stem Cells.

Rajendrarao Sumitha, Venkataswamy M Manjunatha, Rajesh K Sabitha, Phalguni A Alladi, A Nalini, Laxmi T Rao, B K Chandrasekhar Sagar, Harry W M Steinbusch, Boris W Kramer, T N Sathyaprabha and 1 more

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Article in Molecular neurobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 14 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

11 authors at 2 institutions in 2 countries.

Rajendrarao SumithaDepartment of Neurophysiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Venkataswamy M ManjunathaDepartment of Neurovirology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Rajesh K SabithaDepartment of Neurophysiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Phalguni A AlladiDepartment of Neurophysiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
A NaliniDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Laxmi T RaoDepartment of Neurophysiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
B K Chandrasekhar SagarDepartment of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Harry W M SteinbuschSchool of Mental Health and Neuroscience, Maastricht University Medical Center, Maastricht, The Netherlands.
Boris W KramerSchool of Mental Health and Neuroscience, Maastricht University Medical Center, Maastricht, The Netherlands.
T N SathyaprabhaDepartment of Neurophysiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Trichur R RajuDepartment of Neurophysiology, National Institute of Mental Health and Neurosciences, Bengaluru, India. trraju.nimhans@gmail.com.ORCID http://orcid.org/0000-0002-7742-4050
National Institute of Mental Health and Neurosciences · INMaastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disease modeling has become challenging in the context of amyotrophic lateral sclerosis (ALS), as obtaining viable spinal motor neurons from postmortem patient tissue is an unlikely possibility. Limitations in the animal models due to their phylogenetic distance from human species hamper the success of translating possible findings into therapeutic options. Accordingly, there is a need for developing humanized models as a lead towards identifying successful therapeutic possibilities. In this study, human embryonic stem cells-BJNHem20-were differentiated into motor neurons expressing HB9, Islet1, and choline acetyl transferase using retinoic acid and purmorphamine. These motor neurons discharged spontaneous action potentials with two different frequencies (< 5 and > 5 Hz), and majority of them were principal neurons firing with < 5 Hz. Exposure to cerebrospinal fluid from ALS patients for 48 h induced several degenerative changes in the motor neurons as follows: cytoplasmic changes such as beading of neurites and vacuolation; morphological alterations, viz., dilation and vacuolation of mitochondria, curled and closed Golgi architecture, dilated endoplasmic reticulum, and chromatin condensation in the nucleus; lowered activity of different mitochondrial complex enzymes; reduced expression of brain-derived neurotrophic factor; up-regulated neurofilament phosphorylation and hyperexcitability represented by increased number of spikes. All these changes along with the enhanced expression of pro-apoptotic proteins-Bax and caspase 9-culminated in the death of motor neurons.

Indexed as

Cerebrospinal FluidAmyotrophic Lateral SclerosisCells, CulturedEndoplasmic ReticulumFemaleHuman Embryonic Stem CellsHumansIntermediate FilamentsMaleMitochondriaMotor NeuronsNerve DegenerationSpinal CordAmyotrophic lateral sclerosisCerebrospinal fluidHuman embryonic stem cellsMotor neurons

Identifiers

PMID29858777
OpenAlexW2805770517

What OpenQuestion holds

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Registered trials

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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.