Cited by 482Neuroinflammation and Neurodegeneration MechanismsNeurological Disease Mechanisms and TreatmentsMultiple Sclerosis Research Studies

Local distribution of microglia in the normal adult human central nervous system differs by up to one order of magnitude

Mittelbronn, M., Dietz, K., Schluesener, H. J., Meyermann, R.·2001·Acta Neuropathologica

Abstract

Although microglia are considered to be a sensitive sensor for pathological processes in the central nervous system, there are only a few studies about the distribution and density of microglia in the normal human brain. Therefore, a study of local density of microglial cells was conducted by investigating 20 normal human brains with no clinical neurological symptoms or diseases and no neuropathological alterations. Microglial cells were visualized by immunolabeling of proteins which are known to be expressed either constitutively or facultatively, such as CD68, major histocompatibility complex class II (MHC-II), leukocyte common antigen (LCA), leukocyte chemotactic factor (LCF), macrophage inhibitory factor-related protein (MRP) 8, MRP14, CD4 and allograft-inflammatory factor-1 (AIF-1). CD68, MHC-II and AIF-1 showed the highest densities with significant regional differences ranging from 0.5% to 16.6% of all cells in the brain parenchyma with significantly more microglia in white than in gray matter. LCF and LCA showed a similar pattern of distribution as the proteins described above, but with lower percentages of microglial cells. CD4 was not found in the brain parenchyma. We conclude that CD68, MHC-II and AIF-1 define the main microglial cell population, whereas LCF and LCA are expressed by a subpopulation of microglial cells. The brains showed no or a negligible vascular expression of MRP8 and MRP14. Information about the local microglia density in the normal human brain can serve as a reference for the evaluation of pathological microglial responses.

Integrity signals

Registry

Crossref · 10.1007/s004010000284

Cites

5 of 5 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Microglia comprise 0.5-16.6% of the total cell population in the adult brain and spinal cord, depending on anatomical region, sex, and stage of development.

    “Microglia comprise 0.5–16.6% of the total cell population in the adult brain and spinal cord, depending on the anatomical region, sex, and stage of development, among other variables [307,308].”

    From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [307]

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Mittelbronn, M., Dietz, K., Schluesener, H. J., & Meyermann, R.
Affiliations
University of Tübingen (DE)
Corresponding author
Meyermann, R.
Venue
Acta Neuropathologica
Published
2001-03
Volume
101
Issue
3
Pages
249-255
ISSN
  • 0001-6322 (ISSN-L)
  • 1432-0533
OpenAlex
W175813982
Cited by
482
References
5
Citations by year
2026: 19 · 2025: 31 · 2024: 24 · 2023: 32 · 2022: 38 · 2021: 36 · 2020: 36 · 2019: 32 · 2018: 22 · 2017: 38 · 2016: 19 · 2015: 14 · 2014: 21 · 2013: 20 · 2012: 17
FWCI
2.62
Type
journal article
Language
en
Open access
closed
Locations
  • Acta Neuropathologica (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
Keywords
microglia, microglial density, regional distribution, normal human brain, CD68, MHC class II, CD45, S100A8, S100A9, allograft inflammatory factor-1, gray and white matter, microglial subpopulations, brain parenchyma
MeSH terms
CD68 Molecule, Adult, Aged, Aged, 80 and over, Antigens, Differentiation, Brain, Calcium-Binding Proteins, DNA-Binding Proteins, Female, Humans, Immunohistochemistry, Major Histocompatibility Complex, Male, Microfilament Proteins, Middle Aged, S100 Proteins, Reference Values, Antigens, Differentiation, Myelomonocytic, Antigens, CD, CD4 Antigens, Leukocyte Common Antigens, Microglia, Interleukin-16, Calgranulin A, Calgranulin B

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review