Evidence map›Paper›PMID 41659527›Full record

ArticlebioRxiv : the preprint server for biology2026

Injury-transduced SerpinOLs modulate neuroinflammation and glial activation in the diseased and non-diseased CNS.

Yan Wang, Meina Zhu, Joohyun Park, Hyun Kyu Kim, Xiong Ge, Xi Chen, Bo Chen, Shinghua Ding, Wensheng Lin, Fuzheng Guo

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Yan WangDepartment of Neurology, School of Medicine, University of California, Davis.
Meina ZhuDepartment of Neurology, School of Medicine, University of California, Davis.
Joohyun ParkDepartment of Neurology, School of Medicine, University of California, Davis.
Hyun Kyu KimDepartment of Neurology, School of Medicine, University of California, Davis.
Xiong GeDepartment of Neurology, School of Medicine, University of California, Davis.
Xi ChenInstitute of Neurology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Bo ChenDepartment of Neuroscience, Cell Biology and Anatomy, University of Texas Medical Branch, Galveston, TX.
Shinghua DingDepartment of Chemical and Biomedical Engineering, University of Missouri - Columbia.
Wensheng LinDepartment of Neuroscience, University of Minnesota.
Fuzheng GuoDepartment of Neurology, School of Medicine, University of California, Davis.ORCID 0000-0003-3410-8389

Funding

The Role of Gliotransmission in Cerebral IschemiaR01NS069726 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI DING, SHINGHUA · 2010 to 2022
$3.3M
The curious case of PARP1 in CNS myelin formation and repairR01NS123165 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Fuzheng Guo · 2022 to 2026
$2.5M
Glial HIFa: mechanisms and implications in hypoxia/ischemia-induced oligodendroglial pathologyR01NS123080 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GUO, FUZHENG · 2021 to 2025
$2.3M
Pathogenesis and motor neuron degeneration of a novel disease associated with a P158A mutation in NAMPTR01NS123023 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI Shinghua Ding · 2022 to 2026
$2.3M
SOX2-regulated astrocyte homeostasis and pathophysiologyR01NS134887 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Fuzheng Guo · 2024 to 2026
$1.8M
Novel mechanisms of metabolic reprogramming of reactive astrocytes and brain repair after focal cerebral ischemiaR01NS138748 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI Shinghua Ding · 2025 to 2026
$1.2M
Using genetic approaches to explore the role of group I PAKs in developmental myelination of the mammalian CNSR21NS125464 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GUO, FUZHENG · 2022 to 2022
$439k
NINDS NIH HHS R01 NS069726NINDS NIH HHS R01 NS123023NINDS NIH HHS R01 NS123080NINDS NIH HHS R01 NS123165NINDS NIH HHS R01 NS134887NINDS NIH HHS R01 NS138748NINDS NIH HHS R21 NS125464
6 · The paper itself

Abstract

Oligodendroglial dysfunction is common in CNS diseases and injuries, but the molecular and functional responses of oligodendroglia to CNS pathologies remain poorly defined. Here, we report that oligodendrocytes (OLs) respond to demyelinating diseases by dysregulating serine protease inhibitor clade A member 3N (SERPINA3N). Homeostatic OLs transition to Serpina3n-expressing OLs (SerpinOLs) under other diseased conditions including stroke, endotoxicity, neurodegeneration, neurotrauma, and non-diseased healthy aging conditions. Mechanistically, general neuroinflammation or inflammatory mediators is insufficient for SerpinOL transition. Instead, oligodendrocyte damage/injury, even in the absence of neuroinflammation or glial activation, is sufficient for the transition. Phenotypically, SerpinOLs are characterized by molecular signatures of inflammatory and immune regulation and STAT3 signaling activation. Functionally, SerpinOLs exacerbate neuroinflammation and promote glial activation toward pro-inflammatory and neurodegenerative states. Together, our findings suggest SerpinOLs are a common population of injury-transduced OLs that amplify neuroinflammation and glial activation in the diseased and non-diseased CNS through SERPINA3N secretion. Our findings provide new insights into myelination-independent role of OLs in regulating CNS pathophysiology.

Identifiers

PMID41659527
PMCPMC12874004

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.