Evidence map›Paper›PMID 31710637›Full record

ArticlePloS one2019

Optogenetically transduced human ES cell-derived neural progenitors and their neuronal progenies: Phenotypic characterization and responses to optical stimulation.

Jiwon Ryu, Philippe F Y Vincent, Nikolaos K Ziogas, Leyan Xu, Shirin Sadeghpour, John Curtin, Athanasios S Alexandris, Nicholas Stewart, Richard Sima, Sascha du Lac and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. The role of SWI/SNF complexes in digestive system neoplasms.Medical oncology (Northwood, London, England) · 2024
    Review
  3. Optogenetics in Alzheimer's Disease: Focus on Astrocytes.Antioxidants (Basel, Switzerland) · 2023
    Review
  4. Review
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

12 authors at 1 institution in 1 country.

Jiwon RyuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.ORCID 0000-0003-0251-7858
Philippe F Y VincentDepartment of Otolaryngology Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.ORCID 0000-0001-7712-7198
Nikolaos K ZiogasDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Leyan XuDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Shirin SadeghpourDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
John CurtinDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Athanasios S AlexandrisDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.ORCID 0000-0002-5324-8355
Nicholas StewartDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Richard SimaDepartment of Otolaryngology Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.ORCID 0000-0001-7902-2728
Sascha du LacDepartment of Otolaryngology Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Elisabeth GlowatzkiDepartment of Otolaryngology Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Vassilis E KoliatsosDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Johns Hopkins University · US

Funding

AFFERENT SYNAPTIC TRANSMISSION IN THE MAMMALIAN COCHLEAR01DC006476 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI GLOWATZKI, ELISABETH · 2004 to 2022
$6.4M
Cerebellar Output CircuitsR01NS105039 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DU LAC, SASCHA · 2018 to 2022
$1.9M
Synaptic mechanisms underlying vestibular nerve fiber activityR01DC012957 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI GLOWATZKI, ELISABETH · 2014 to 2018
$1.9M
NIDCD NIH HHS R01 DC006476NIDCD NIH HHS R01 DC012957
6 · The paper itself

Abstract

Optogenetically engineered human neural progenitors (hNPs) are viewed as promising tools in regenerative neuroscience because they allow the testing of the ability of hNPs to integrate within nervous system of an appropriate host not only structurally, but also functionally based on the responses of their differentiated progenies to light. Here, we transduced H9 embryonic stem cell-derived hNPs with a lentivirus harboring human channelrhodopsin (hChR2) and differentiated them into a forebrain lineage. We extensively characterized the fate and optogenetic functionality of hChR2-hNPs in vitro with electrophysiology and immunocytochemistry. We also explored whether the in vivo phenotype of ChR2-hNPs conforms to in vitro observations by grafting them into the frontal neocortex of rodents and analyzing their survival and neuronal differentiation. Human ChR2-hNPs acquired neuronal phenotypes (TUJ1, MAP2, SMI-312, and synapsin 1 immunoreactivity) in vitro after an average of 70 days of coculturing with CD1 astrocytes and progressively displayed both inhibitory and excitatory neurotransmitter signatures by immunocytochemistry and whole-cell patch clamp recording. Three months after transplantation into motor cortex of naïve or injured mice, 60-70% of hChR2-hNPs at the transplantation site expressed TUJ1 and had neuronal cytologies, whereas 60% of cells also expressed ChR2. Transplant-derived neurons extended axons through major commissural and descending tracts and issued synaptophysin+ terminals in the claustrum, endopiriform area, and corresponding insular and piriform cortices. There was no apparent difference in engraftment, differentiation, or connectivity patterns between injured and sham subjects. Same trends were observed in a second rodent host, i.e. rat, where we employed longer survival times and found that the majority of grafted hChR2-hNPs differentiated into GABAergic neurons that established dense terminal fields and innervated mostly dendritic profiles in host cortical neurons. In physiological experiments, human ChR2+ neurons in culture generated spontaneous action potentials (APs) 100-170 days into differentiation and their firing activity was consistently driven by optical stimulation. Stimulation generated glutamatergic and GABAergic postsynaptic activity in neighboring ChR2- cells, evidence that hChR2-hNP-derived neurons had established functional synaptic connections with other neurons in culture. Light stimulation of hChR2-hNP transplants in vivo generated complicated results, in part because of the variable response of the transplants themselves. Our findings show that we can successfully derive hNPs with optogenetic properties that are fully transferrable to their differentiated neuronal progenies. We also show that these progenies have substantial neurotransmitter plasticity in vitro, whereas in vivo they mostly differentiate into inhibitory GABAergic neurons. Furthermore, neurons derived from hNPs have the capacity of establishing functional synapses with postsynaptic neurons in vitro, but this outcome is technically challenging to explore in vivo. We propose that optogenetically endowed hNPs hold great promise as tools to explore de novo circuit formation in the brain and, in the future, perhaps launch a new generation of neuromodulatory therapies.

Indexed as

OptogeneticsAnimalsAstrocytesAxonsCell DifferentiationCell LineageCell SurvivalChannelrhodopsinsHuman Embryonic Stem CellsHumansLentivirusLightMice, NudeMotor CortexNeural Stem CellsNeuronal PlasticityChannelrhodopsinsNeurotransmitter Agents

Identifiers

PMID31710637
PMCPMC6844486
OpenAlexW2986661580

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.