Evidence map›Paper›PMID 29577367›Full record

ArticleJournal of neuroscience research2020

Bioluminescence-driven optogenetic activation of transplanted neural precursor cells improves motor deficits in a Parkinson's disease mouse model.

Jessica R Zenchak, Brandon Palmateer, Nicolai Dorka, Tariq M Brown, Lina-Marie Wagner, William E Medendorp, Eric D Petersen, Mansi Prakash, Ute Hochgeschwender

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroscience research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. CaBLAM! A high-contrast bioluminescent CabioRxiv : the preprint server for biology · 2025
    Article
  3. Article
  4. Application of Optogenetics in Neurodegenerative Diseases.Cellular and molecular neurobiology · 2024
    Review
  5. Bioluminescent Systems for Theranostic Applications.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Engineering luminopsins with improved coupling efficiencies.bioRxiv : the preprint server for biology · 2023
    Article
  9. Article
  10. Article
  11. Review
  12. EndogenousNeural regeneration research · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Applications of Bioluminescence-Optogenetics in Rodent Models.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Jessica R ZenchakNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Brandon PalmateerNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Nicolai DorkaNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Tariq M BrownNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Lina-Marie WagnerNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
William E MedendorpNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Eric D PetersenNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Mansi PrakashNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.
Ute HochgeschwenderNeuroscience Program, Central Michigan University, Mt. Pleasant, Michigan.ORCID 0000-0001-5165-6518
Central Michigan University · US

Funding

BioLuminescent OptoGenetics (BL-OG): A Novel and Versatile Strategy for NeuromodulationU01NS099709 · NINDS · CENTRAL MICHIGAN UNIVERSITY · PI HOCHGESCHWENDER, UTE H, MOORE, CHRISTOPHER I · 2016 to 2018
$2.4M
Employing subcellular calcium to control membrane voltageR21EY026427 · NEI · CENTRAL MICHIGAN UNIVERSITY · PI HOCHGESCHWENDER, UTE H, LIPSCOMBE, DIANE · 2015 to 2016
$472k
A transgenic platform for highly specific and remote control of neuronal activityR21MH093914 · NIMH · DUKE UNIVERSITY · PI HOCHGESCHWENDER, UTE H · 2011 to 2012
$438k
Genetically Encoded Light-Production and Light-Sensing for Neuronal ManipulationR21MH101525 · NIMH · DUKE UNIVERSITY · PI HOCHGESCHWENDER, UTE H · 2013 to 2015
$434k
Deriving ES Cell Lines from a Down Syndrome Mouse ModelR03HD046913 · NICHD · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI HOCHGESCHWENDER, UTE H · 2005 to 2006
$153k
Central Michigan UniversityDAAD RISE "Research Internships in Science and Engineering" Research FellowshipDivision of Chemical, Bioengineering, Environmental, and Transport SystemsGraduate Student Research & Creative Endeavors GrantMcNair Scholars Program (TMB)NEI NIH HHS R21 EY026427NICHD NIH HHS R03 HD046913NIMH NIH HHS R21 MH093914NIMH NIH HHS R21 MH101525NINDS NIH HHS U01 NS099709RISEThe CMU Office of Research and Graduate StudiesThe National Institutes of Health R21EY026427The National Institutes of Health R21MH101525The National Institutes of Health U01NS099709The National Science Foundation CBET-1464686Undergraduate Summer Scholars Program
6 · The paper itself

Abstract

The need to develop efficient therapies for neurodegenerative diseases is urgent, especially given the increasing percentages of the population living longer, with increasing chances of being afflicted with conditions like Parkinson's disease (PD). A promising curative approach toward PD and other neurodegenerative diseases is the transplantation of stem cells to halt and potentially reverse neuronal degeneration. However, stem cell therapy does not consistently lead to improvement for patients. Using remote stimulation to optogenetically activate transplanted cells, we attempted to improve behavioral outcomes of stem cell transplantation. We generated a neuronal precursor cell line expressing luminopsin 3 (LMO3), a luciferase-channelrhodopsin fusion protein, which responds to the luciferase substrate coelenterazine (CTZ) with emission of blue light that in turn activates the opsin. Neuronal precursor cells were injected bilaterally into the striatum of homozygous aphakia mice, which carry a spontaneous mutation leading to lack of dopaminergic neurons and symptoms of PD. Following transplantation, the cells were stimulated over a period of 10 days by intraventricular injections of CTZ. Mice receiving CTZ demonstrated significantly improved motor skills in a rotarod test compared to mice receiving vehicle. Thus, bioluminescent optogenetic stimulation of transplanted neuronal precursor cells shows promising effects in improving locomotor behavior in the aphakia PD mouse model and encourages further studies to elucidate the mechanisms and long-term outcomes of these beneficial effects.

Indexed as

Luminescent ProteinsMotor ActivityAnimalsDisease Models, AnimalFemaleImidazolesLuminescent AgentsLuminescent MeasurementsMaleMice, TransgenicNeural Stem CellsOpsinsOptogeneticsParkinson DiseasePyrazinesRotarod Performance TestcoelenterazineImidazolesLuminescent AgentsLuminescent ProteinsOpsinsPyrazineschemogeneticembryonic stem cellsluminopsinmultielectrode arrayneural differentiationPitx3

Identifiers

PMID29577367
PMCPMC6157008
OpenAlexW2793759392

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.