Evidence map›Paper›PMID 42113447›Full record

ArticleScience China. Life sciences2026

Proteomic comparison of human neural cell-derived extracellular vesicles and parental cells from Alzheimer's disease and cognitively normal individuals.

Jia-Yan Xin, Jie Liu, Hao-Min Dong, Hai-Lun Yu, Zhong-Song Xiao, Jian-Ni Hu, Qiu Jiang, Yu-Peng Zhu, Lin Feng, Yun Feng and 12 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Science China. Life sciences, 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

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

22 authors.

Jia-Yan Xin *Department of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Jie Liu *Department of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Hao-Min Dong *Department of Cognitive Impairment Research, Chongqing Institute for Brain and Intelligence, Guangyang Bay Laboratory, Chongqing, 401336, China.
Hai-Lun YuCarrier Biomed (Suzhou) Co., Ltd., Suzhou, 215000, China.
Zhong-Song XiaoDepartment of Cognitive Impairment Research, Chongqing Institute for Brain and Intelligence, Guangyang Bay Laboratory, Chongqing, 401336, China.
Jian-Ni HuDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Qiu JiangDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Yu-Peng ZhuDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Lin FengDepartment of Cognitive Impairment Research, Chongqing Institute for Brain and Intelligence, Guangyang Bay Laboratory, Chongqing, 401336, China.
Yun FengDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Yu-Juan JiaDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Zi-Yu YuanDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Zhong-Yuan YuDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
An-Yu ShiDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Gui-Hua ZengDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Jun WangDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China.
Wen-Yuan WangInterdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, 201210, China.
Lesley ChengDepartment of Biochemistry and Chemistry, La Trobe Institute for Molecular Science, La Trobe University, Bundoora, Victoria, 3086, Australia.
Laura J VellaThe Florey Institute, The University of Melbourne, Parkville, Victoria, 3052, Australia.
Frederic Zhentao LiCarrier Biomed (Suzhou) Co., Ltd., Suzhou, 215000, China.
Colin L MastersThe Florey Institute, The University of Melbourne, Parkville, Victoria, 3052, Australia. c.masters@florey.edu.au.
Yan-Jiang WangDepartment of Neurology and Center for Clinical Neuroscience, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, 400042, China. yanjiang_wang@tmmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating brain-derived extracellular vesicles (BDEVs) have emerged as promising biomarkers for neurodegenerative diseases, including Alzheimer's disease (AD). However, it remains unclear to what extent extracellular vesicles (EVs) proteomes reflect the molecular states and disease-associated alterations of their parent brain cell types. Here, using a multi-line human induced pluripotent stem cell (hiPSC) platform derived from three AD and three cognitively normal (CN) donors, we generated neurons, astrocytes, microglia, and oligodendrocytes, and performed paired proteomic profiling of each cell type and its secreted EVs. We systematically compared protein profiles to evaluate cell-EV similarity, disease-associated features, and concordance with proteomic datasets from human AD brain tissue. Across all four lineages, EV proteomes showed extensive overlap with parent cells (>97% overlap; Jaccard index: 0.69-0.80) while also displaying lineage-specific functional biases. Under AD versus CN comparisons, EVs exhibited larger effect sizes and retained a higher number of differentially expressed proteins (DEPs) when applying the same fold-change criteria, yielding clearer AD-CN separation than their parent cells. Importantly, EV DEPs showed higher concordance with human AD brain proteomic signatures (EVs: 2,134 DEPs; cells: 816 DEPs). Finally, amyloid precursor protein (APP)-derived peptides, including amyloid-β (Aβ), were preferentially enriched in neuron- and oligodendrocyte-derived EVs, and AD EVs showed elevated Aβ42, p-Tau217 and p-Tau181 relative to CN EVs. Together, these data indicate that cell type-resolved EV proteomes largely recapitulate parent cell identity while sensitively capturing AD-relevant molecular alterations, supporting EV-based strategies for early diagnosis and monitoring of AD and potentially other neurodegenerative disorders.

Indexed as

Alzheimer DiseaseExtracellular VesiclesNeuronsProteomeProteomicsAmyloid beta-PeptidesAstrocytesBiomarkersBrainHumansInduced Pluripotent Stem CellsMicrogliaOligodendrogliaAmyloid beta-PeptidesBiomarkersProteomeAlzheimer’s diseasebiomarkersbrain-derived extracellular vesiclesdiagnosisliquid biopsyproteomics

Identifiers

PMID42113447

What Socratic holds

Textmetadata
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.