Evidence map›Paper›PMID 25193935›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2014

Ontogeny and functions of central nervous system macrophages.

Atsuko Katsumoto, Haiyan Lu, Aline S Miranda, Richard M Ransohoff

Abstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing 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

77 citing papers in PubMed.

  1. Review
  2. Article
  3. Revisiting the critical roles of reactive microglia in traumatic brain injury.International journal of surgery (London, England) · 2025
    Review
  4. Preclinical characterization of [Acta pharmacologica Sinica · 2025
    Article
  5. Review
  6. Article
  7. Current neuropharmacology · 2024
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. The potential roles of mJournal of neuroinflammation · 2021
    Article
  17. Article
  18. Review
  19. Decoding Mast Cell-Microglia Communication in Neurodegenerative Diseases.International journal of molecular sciences · 2021
    Review
  20. Article

17 more citing papers are in PubMed but not listed here.

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

4 authors.

Atsuko KatsumotoNeuroinflammation Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195; and.
Haiyan LuNeuroinflammation Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195; and.
Aline S MirandaNeuroinflammation Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195; and.
Richard M RansohoffNeuroinflammation Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195; and Mellen Center for Multiple Sclerosis Treatment and Research, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195 ransohr@ccf.org.

Funding

CHEMOKINES IN CNS INFLAMMATIONR01NS032151 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI RANSOHOFF, RICHARD M. · 1994 to 2013
$3.7M
Drugs of abuse and the epigenetic and signaling pathways controlling HIV latencyR01DA036171 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI GOLDSTEIN, HARRIS, HARVEY, BRANDON K · 2013 to 2017
$3.6M
The role of fractalkine signaling in neurodegenerative diseaseR01NS074804 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI LAMB, BRUCE T, RANSOHOFF, RICHARD M. · 2011 to 2015
$1.7M
Myeloid cells, aging and the metabolic syndromeR21AG046399 · NIA · CLEVELAND CLINIC LERNER COM-CWRU · PI LI, XIAOXIA, RANSOHOFF, RICHARD M. · 2013 to 2014
$436k
The Role of Monocytes and Microglia in Traumatic Brain Injury-Induced TauopathiesR21NS082798 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI LAMB, BRUCE T, RANSOHOFF, RICHARD M. · 2013 to 2014
$434k
NIA NIH HHS R21 AG046399NIDA NIH HHS R01 DA036171NINDS NIH HHS R01 NS032151NINDS NIH HHS R01 NS074804NINDS NIH HHS R21 NS082798
6 · The paper itself

Abstract

Microglia, the only nonneuroepithelial cells found in the parenchyma of the CNS, originate during embryogenesis from the yolk sac and enter the CNS quite early (embryonic day 9.5-10 in mice). Thereafter, microglia are maintained independently of any input from the blood and, in particular, do not require hematopoietic stem cells as a source of replacement for senescent cells. Monocytes are hematopoietic cells, derived from bone marrow. The ontogeny of microglia and monocytes is important for understanding CNS pathologies. Microglial functions are distinct from those of blood-derived monocytes, which invade the CNS only under pathological conditions. Recent data reveal that microglia play an important role in managing neuronal cell death, neurogenesis, and synaptic interactions. In this article, we discuss the physiology of microglia and the functions of monocytes in CNS pathology. We address the roles of microglia and monocytes in neurodegenerative diseases as an example of CNS pathology.

Indexed as

AnimalsApoptosisCell CommunicationCell DifferentiationCell LineageCentral Nervous SystemHumansMacrophagesMiceMicrogliaNeurodegenerative DiseasesNeurogenesis

Identifiers

PMID25193935
PMCPMC4157312

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.