Evidence map›Paper›PMID 41689059›Full record

ArticleMolecular neurodegeneration2026

The functional role of glial cells in the pathologic brain as reviewed by Alois Alzheimer in 1910.

Helmut Kettenmann, Hans Lassmann, Bilge Ugursu, Xianyuan Xiang

Abstract readHistorical Article
In one paragraph

Article in Molecular neurodegeneration, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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.

Helmut KettenmannBio-X International Institute, Faculty of Life and Health Sciences, Shenzhen University of Advanced Technology, Shenzhen, China. kettenmann@suat-sz.edu.cn.
Hans LassmannCenter for Brain Research, Medical University of Vienna, Vienna, Austria.
Bilge UgursuMax-Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Xianyuan XiangBio-X International Institute, Faculty of Life and Health Sciences, Shenzhen University of Advanced Technology, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alois Alzheimer is known for the clinical diagnosis and neuropathological analysis of the neurodegenerative disease named after him. Yet, a less celebrated but equally fundamental contribution lies in his monograph, “Contributions to the knowledge of the pathologic neuroglia and their relationship to degenerative processes in the nervous tissue.” This work, now translated, meticulously details the dynamic role of glial cells in brain pathology, a paradigm-shifting concept for its time. Alzheimer applied then-novel staining techniques -including adaptations of Scharlach red and Mallory hematoxylin- to visualize lipids and protoplasmic degradation in post-mortem human brains. These approaches revealed striking changes in the glial network across disorders ranging from stroke and trauma to multiple sclerosis, syphilis-related dementia, various forms of neurodegeneration, and schizophrenia. He documented the appearance of two novel glial forms, which he termed “ameboid glia” and “glial granule cells”, involved in the phagocytosis of “fatty matter” and “lipoid substances” from degenerating nervous tissue. He also documented “neuronophagia,” where glial cells appeared to directly interact with and “dissolve” damaged neurons. This work laid the conceptual groundwork for modern neuroscience. We now recognize Alzheimer’s “ameboid glia” as the earliest documented observations of activated microglia and astrocytes, and his descriptions of glia’s engagement with cellular damage provided the first evidence for what we now call neuroinflammation. His methodical approach and detailed observations proved that glial cells are not passive bystanders but central, active players that sense, respond to, and shape the course of brain diseases. The English translation and the original German text can be found in the attachment.

Indexed as

Alzheimer DiseaseBrainNeurogliaAnimalsHistory, 20th CenturyHumansReview Literature as TopicAlois AlzheimerAmeboid gliaAstrocytesGlial granule cellsMicrogliaNeuroinflammationPathologic neuroglia

Identifiers

PMID41689059
PMCPMC13005332

What Socratic holds

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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 Socratic graph.