Evidence map›Paper›PMID 30801863›Full record

ReviewStem cells (Dayton, Ohio)2019

Concise Review: Modeling Neurodegenerative Diseases with Human Pluripotent Stem Cell-Derived Microglia.

Walther Haenseler, Lawrence Rajendran

Open access · bronzeAbstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Review
  3. Research models to study lewy body dementia.Molecular neurodegeneration · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Human Induced Pluripotent Stem Cell-Derived Microglia (hiPSC-Microglia).Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Synthetic human livers for modeling metabolic diseases.Current opinion in gastroenterology · 2021
    Review
  20. 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

2 authors at 2 institutions in 2 countries.

Walther HaenselerSystems and Cell Biology of Neurodegeneration, IREM, University of Zurich, Schlieren, Switzerland.ORCID 0000-0003-4868-3704
Lawrence RajendranSystems and Cell Biology of Neurodegeneration, IREM, University of Zurich, Schlieren, Switzerland.
King's College London · GBUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammation of the brain and the consequential immunological responses play pivotal roles in neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, and frontotemporal dementia (FTD). Microglia, the resident macrophage cells of the brain, have also emerged as key players in neuroinflammation. As primary human microglia from living subjects are normally not accessible to researchers, there is a pressing need for an alternative source of authentic human microglia which allows modeling of neurodegeneration in vitro. Several protocols for induced pluripotent stem cell (iPSC)-derived microglia have recently been developed and provide unlimited access to patient-derived material. In this present study, we give an overview of iPSC-derived microglia models in monoculture and coculture systems, their advantages and limitations, and how they have already been used for disease phenotyping. Furthermore, we outline some of the gene engineering tools to generate isogenic controls, the creation of gene knockout iPSC lines, as well as covering reporter cell lines, which could help to elucidate complex cell interaction mechanisms in the microglia/neuron coculture system, for example, microglia-induced synapse loss. Finally, we deliberate on how said cocultures could aid in personalized drug screening to identify patient-specific therapies against neurodegeneration. Stem Cells 2019;37:724-730.

Indexed as

Alzheimer DiseaseAmyotrophic Lateral SclerosisCell- and Tissue-Based TherapyCoculture TechniquesFrontotemporal DementiaGene Knockout TechniquesGenetic EngineeringHigh-Throughput Screening AssaysHumansInduced Pluripotent Stem CellsInflammationMicrogliaModels, BiologicalNeuronsNeuroprotective AgentsNootropic AgentsNeuroprotective AgentsNootropic AgentsExperimental modelsGliaInduced pluripotent stem cellsMyeloid cellsNeuroimmuneYolk sac cell

Identifiers

PMID30801863
PMCPMC6849818
OpenAlexW2917982873

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.