Evidence map›Paper›PMID 41814352›Full record

ArticleMicrobiome2026

Agarose oligosaccharides balance intestinal stem cell homeostasis in aging D. melanogaster by regulating the Acetobacter persici-acetic acid-JAK/STAT signaling axis.

Shuhang Fan, Qiyu Xu, Qianyi Zhang, Jiayi She, Cheng Zhang, Mark Christian, Zhenyu Wang, Xianjun Dai

Abstract read
In one paragraph

Article in Microbiome, 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

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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Shuhang Fan *College of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Qiyu Xu *College of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Qianyi ZhangCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Jiayi SheCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Cheng ZhangCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China.
Mark ChristianSchool of Science and Technology, Nottingham Trent University, Clifton, Nottingham, NG11 8NS, UK.
Zhenyu WangCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China. mrwangzyu@cjlu.edu.cn.
Xianjun DaiCollege of Life Sciences, China Jiliang University, Hangzhou, 310018, China. xjdai@cjlu.edu.cn.

Funding

Fundamental Research Funds for the Provincial Universities of Zhejiang No. 2024YW56National Key Research and Development Program of China No. 2024YFF1106203Project of Innovation and Entrepreneurship Training for National Undergraduates No. 202310356045Science and Technology Development Project in Zhejiang No. 2022C01030Zhejiang Provincial Natural Science Foundation No. LQN25C200002
6 · The paper itself

Abstract

backgroundIntestinal aging manifests as the decline in gut function and structure, affecting nutrient absorption and overall health. Agarose oligosaccharides (AOS) exhibit considerable anti-aging effects, but their mechanism of action remains unclear.

resultsHere, aging male Drosophila melanogaster (D. melanogaster) were employed to evaluate the effects of AOS on the proliferation and differentiation of intestinal stem cell (ISC) and its underlying mechanism. Our findings revealed that supplementation with AOS significantly extended mean and maximum lifespan, reduced oxidative stress, and alleviated intestinal epithelial barrier dysfunction. Notably, AOS supplementation reduced the mean fluorescence intensity of esg⁺ cells and enteroblasts (EB), leading to an improvement in ISC homeostasis, with potential mechanisms associated with activation of the PERK and JAK/STAT signaling pathways, as demonstrated by RNA interference. Integrated 16S rRNA sequencing, strain isolation, and short-chain fatty acids (SCFAs) analysis revealed that AOS was beneficial for intestinal microflora and its metabolites, evidenced by the significant increase in Acetobacter persici and acetic acid contents. Importantly, further experiments demonstrated that Acetobacter persici and acetic acid treatment could significantly decrease the esg⁺ ISC count and downregulate the expression levels of PERK, STAT, and Hsp70Bbb, suggesting that AOS can increase production of Acetobacter persici and its metabolite acetic acid, thereby modulating JAK/STAT signaling to improve ISC steady-state.

conclusionsThe homeostasis of ISC in aging D. melanogaster is balanced by AOS via the acetic acid-JAK/STAT axis mediated by Acetobacter persici. This axis counters age-related ISC dysregulation by balancing proliferative signals with redox homeostasis, positioning AOS as a microbiota-targeted intervention for age-associated intestinal decline.

Indexed as

Acetic AcidAcetobacterAgingDrosophila melanogasterIntestinesOligosaccharidesStem CellsAnimalsCell DifferentiationCell ProliferationDrosophila ProteinsGastrointestinal MicrobiomeHomeostasisJanus KinasesMaleOxidative StressAcetic AcidDrosophila ProteinsJanus KinasesOligosaccharidesRNA, Ribosomal, 16SSTAT Transcription FactorsAcetic acidAcetobacter persiciAgarose oligosaccharidesAgingD. melanogasterIntestinal stem cell

Identifiers

PMID41814352
PMCPMC12994225

What OpenQuestion 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 OpenQuestion graph.