Evidence map›Paper›PMID 33085226›Full record

ReviewImmunity, inflammation and disease2020

What has single-cell RNA sequencing revealed about microglial neuroimmunology?

Norwin Kubick, Patrick C Henckell Flournoy, Pavel Klimovich, Gina Manda, Michel-Edwar Mickael

Abstract readReview
In one paragraph

Review in Immunity, inflammation and disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. The Journey of Cancer Cells to the Brain: Challenges and Opportunities.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Microglia in brain development and regeneration.Development (Cambridge, England) · 2022
    Review
  11. CD4Neural regeneration research · 2021
    Article
  12. Article
  13. 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

5 authors.

Norwin KubickDepartment of Biochemistry and Molecular Cell Biology (IBMZ), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Patrick C Henckell FlournoyDepartment of Immunology, PM Research Center, Stockholm, Ekerö, Sweden.
Pavel KlimovichDepartment of Immunology, PM Research Center, Stockholm, Ekerö, Sweden.
Gina MandaDepartment of Radiology, Victor Babes National Institute of Pathology, Bucharest, Romania.
Michel-Edwar MickaelDepartment of Immunology, PM Research Center, Stockholm, Ekerö, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of single-cell RNA sequencing (scRNA-seq) in microglial research is increasing rapidly. The basic workflow of this approach consists of isolating single cells, followed by sequencing. scRNA-seq is capable of examining microglial heterogeneity on a cellular level. However, the results gained from applying this technique suffer from discrepancies due to differences between applied methods characteristics such as the number of cells sequenced and the depth of sequencing. This review aims to shed more light on the recent developments that happened in this field and how they are related to the methods used. To do that, we track the progress and limitations of various scRNA-seq methods currently available. The review then summarizes the current knowledge gained using scRNA-seq in the field of microglia, including novel subpopulations associated with function and development under homeostasis as well during several pathological conditions such as Alzheimer, lipopolysaccharide response, and HIV in relation to the methods employed. Our review points out that despite major developments found using this technique, current scRNA-seq methods suffer from high cost, low yields, and nonstandardization of generated data. Additional development of scRNA-seq methods will raise our awareness of microglia's heterogeneity and plasticity under healthy and pathological conditions.

Indexed as

MicrogliaNeurodegenerative DiseasesAnimalsGene Expression ProfilingHumansSequence Analysis, RNASingle-Cell AnalysisSoftwaremicrogliasingle-cell RNA sequencingT cells

Identifiers

PMID33085226
PMCPMC7654416

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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.