Evidence map›Paper›PMID 24459672›Full record

ArticleBioMed research international2013

Site-specific distribution of CD68-positive microglial cells in the brains of human midterm fetuses: a topographical relationship with growing axons.

Kwang Ho Cho, Jin Sung Cheong, Ji Hyun Kim, Hiroshi Abe, Gen Murakami, Baik Hwan Cho

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Glial cells in the mammalian olfactory bulb.Frontiers in cellular neuroscience · 2024
    Review
  3. Microglia in brain development and regeneration.Development (Cambridge, England) · 2022
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  6. Article
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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

6 authors at 4 institutions in 2 countries.

Kwang Ho ChoDepartment of Neurology, Jeonbuk Regional Cardiocerebrovascular Disease Center, Institute of Wonkwang Medical Science, Wonkwang University School of Medicine, Iksan 570-711, Republic of Korea.
Jin Sung CheongDepartment of Neurology, Jeonbuk Regional Cardiocerebrovascular Disease Center, Institute of Wonkwang Medical Science, Wonkwang University School of Medicine, Iksan 570-711, Republic of Korea.
Ji Hyun KimDepartment of Anatomy, Chonbuk National University School of Medicine, 634-18 Geumam-dong, Deokjin-gu, Jeonju 561-712, Republic of Korea.
Hiroshi AbeDepartment of Anatomy, Akita University School of Medicine, Akita 010-8502, Japan.
Gen MurakamiDivision of Internal Medicine, Iwamizawa Kojin-kai Hospital, Iwamizawa 068-0833, Japan.
Baik Hwan ChoDepartment of Surgery, Chonbuk National University School of Medicine, 634-18 Geumam-dong, Deokjin-gu, Jeonju 561-712, Republic of Korea.
Jeonbuk National University · KRWonkwang University · KRAkita University · JPMiwa Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using 5 fetuses of gestational age (GA) of 15-16 weeks and 4 of GA of 22-25 weeks, we examined site- and stage-dependent differences in CD68-positive microglial cell distribution in human fetal brains. CD68 positive cells were evident in the floor of the fourth ventricle and the pons and olive at 15-16 weeks, accumulating in and around the hippocampus at 22-25 weeks. At both stages, the accumulation of these cells was evident around the optic tract and the anterior limb of the internal capsule. When we compared CD68-positive cell distribution with the topographical anatomy of GAP43-positive developing axons, we found that positive axons were usually unaccompanied by CD68-positive cells, except in the transpontine corticofugal tract and the anterior limb of the internal capsule. Likewise, microglial cell distribution did not correspond with habenulointerpeduncular tract. Therefore, the distribution of CD68-positive cells during normal brain development may not reflect a supportive role of these microglia in axonogenesis of midterm human fetuses.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticAxonsBrainCD68 MoleculeFemaleFetusGestational AgeHumansMicrogliaPregnancyAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 Molecule

Identifiers

PMID24459672
PMCPMC3891602
OpenAlexW2078839260

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.