Evidence map›Paper›PMID 41299697›Full record

ArticleCell communication and signaling : CCS2025

Extracellular vesicles for delivery of functional telomerase.

Yingying He, Yumeng Cui, Lijuan Wang, Wen Yang, Ruping Wang, Yanghua Li, Yue Ma, Yanli Lin, Xiaojie Wu, Long Cheng and 2 more

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. 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

12 authors.

Yingying He *Baotou Medical College, Baotou, 014040, China.
Yumeng Cui *Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, 100071, China.
Lijuan Wang *Baotou Medical College, Baotou, 014040, China.
Wen Yang *Department of Third General Surgery, Lanzhou Second People's Hospital, Lanzhou, 730046, China.
Ruping WangBaotou Medical College, Baotou, 014040, China.
Yanghua LiLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, 100071, China.
Yue MaLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, 100071, China.
Yanli LinLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, 100071, China.
Xiaojie WuLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, 100071, China.
Long ChengThe Key Laboratory of Geriatrics, Institute of Geriatric Medicine, Beijing Institute of Geriatrics, Chinese Academy of Medical Sciences, Beijing Hospital/National Centre of Gerontology of National Health Commission, Beijing, 100730, China.
Chengjiang ZhouBaotou Medical College, Baotou, 014040, China. 81827358@qq.com.
Youliang WangLaboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, 100071, China. wang_you_liang@aliyun.com.

Funding

Baotou Medical College High-Level Talent Research Fund Project BYJJ-GCC 202502National Key Research and Development Program 2022YFC3600100
6 · The paper itself

Abstract

backgroundTelomerase, essential for maintaining chromosomal telomere integrity and preventing cellular senescence, represents a promising therapeutic target. However, the inherent risks associated with existing treatments for telomerase deficiency-related diseases necessitate the development of safe and precise targeted delivery systems capable of reaching specific cell populations. Extracellular vesicles (EVs), nanoscale membrane-bound particles naturally secreted by cells, mediate intercellular communication by transporting bioactive molecules, including proteins and nucleic acids. We hypothesized that EVs could function as intrinsic vehicles for telomerase delivery.

methodsTo investigate this, we demonstrated the effective encapsulation of functional telomerase components, specifically TERT and TERC, within EVs. Furthermore, we observed that enhanced TERT expression led to increased telomerase activity within the EVs, as confirmed by TRAP assay results.

resultsThese telomerase-loaded EVs, leveraging their inherent targeting capabilities and unique vesicular structure, efficiently delivered the active enzyme to recipient cells. In aged mice, delivery of telomerase via EVs restored endogenous telomerase activity, preserved telomere integrity, and attenuated senescence across multiple tissues. We observed that the internalized telomerase modulated the expression of senescence-associated markers, thereby delaying cellular aging and promoting cellular proliferation.

conclusionsThese findings support the feasibility of EV-mediated intercellular telomerase delivery, suggesting a potential avenue for developing therapeutic interventions for pathologies associated with telomerase deficiency.

Indexed as

Cellular SenescenceDrug CarriersExtracellular VesiclesTelomeraseAnimalsFemaleHeLa CellsHumansMaleMiceMice, Inbred C57BLRNATelomere HomeostasisDrug CarriersRNATelomerasetelomerase RNACellular senescenceExtracellular vesiclesTelomeraseTERT

Identifiers

PMID41299697
PMCPMC12659060

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.