Evidence map›Paper›PMID 42438074›Full record

ReviewThe FEBS journal2026

Combating ageing beyond the cell: Emerging roles of extracellular proteostasis.

Siddharth R Venkatesh, Ivan Gallotta, Bolanle F Olabiyi, Yoon Hee Choi, Sarah Inglesfield, Janet R Kumita, Collin Y Ewald, Della C David

Abstract readReview
In one paragraph

Review in The FEBS journal, 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. 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

8 authors.

Siddharth R VenkateshSignalling Programme, Babraham Institute, Cambridge, UK.ORCID https://orcid.org/0000-0002-0393-2036
Ivan GallottaSignalling Programme, Babraham Institute, Cambridge, UK.ORCID https://orcid.org/0009-0008-1521-2029
Bolanle F OlabiyiSignalling Programme, Babraham Institute, Cambridge, UK.ORCID https://orcid.org/0000-0001-5753-5143
Yoon Hee ChoiSignalling Programme, Babraham Institute, Cambridge, UK.ORCID https://orcid.org/0000-0002-4740-3937
Sarah InglesfieldBioinformatics Facility, Babraham Institute, Cambridge, UK.ORCID https://orcid.org/0000-0002-3511-9090
Janet R KumitaDepartment of Pharmacology, University of Cambridge, UK.ORCID https://orcid.org/0000-0002-3887-4964
Collin Y EwaldLaboratory of Extracellular Matrix Regeneration, Institute of Translational Medicine, Department of Health Sciences and Technology, ETH Zürich, Schwerzenbach, Switzerland.ORCID https://orcid.org/0000-0003-1166-4171
Della C DavidSignalling Programme, Babraham Institute, Cambridge, UK.ORCID https://orcid.org/0000-0001-8597-9470

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/000C0531Medical Research Council MR/W01632X/1Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung P3 Project 190072Wellcome TrustWellcome Trust 225838/Z/22/Z
6 · The paper itself

Abstract

Proteostasis, the maintenance of a healthy proteome, is a fundamental pillar of cellular and organismal health that declines with age. While the intracellular proteostasis network (PN) is well-characterised, proteostasis mechanisms acting in the extracellular space remain understudied. Yet, these mechanisms face unique challenges and are critical for ensuring functional systemic signalling, immune surveillance and structural integrity. In contrast to the cytosol, extracellular environments lack ATP-activated chaperones and a comprehensive ubiquitin-proteasome system and instead rely on specialised secreted chaperones, extracellular proteases and receptor-mediated clearance mechanisms. This review examines the emerging landscape of the extracellular proteostasis network (exPN) and its challenges with age. We discuss how age-related remodelling of the extracellular proteome, shifts in extracellular physicochemical properties and disrupted fluid dynamics collectively create a permissive environment for protein misfolding and aggregation. We evaluate current experimental models of extracellular protein damage and examine how exPN factors target specific stages of the aggregation process to cooperatively safeguard extracellular proteome integrity. Analysis of recent human proteomic data spanning the life course uncovers an unexpected upregulation of exPN components with age. We further explore the role of extracellular proteostasis in inflammageing, a defining hallmark of ageing. Finally, we highlight strategies that bolster extracellular proteostasis as a promising frontier for extending healthspan, limiting age-associated protein aggregation and restoring extracellular matrix homeostasis. By adopting an ageing-centred perspective, we move beyond the disease context to present a holistic overview of extracellular proteostasis in organismal health, thereby positioning the exPN as a critical yet under-exploited target for biomedical intervention.

Indexed as

AgingProteomeProteostasisAnimalsExtracellular SpaceHumansMolecular ChaperonesProteasome Endopeptidase ComplexProtein FoldingProteotoxic StressMolecular ChaperonesProteasome Endopeptidase ComplexProteomeageingextracellular chaperonesextracellular matrixextracellular proteasesextracellular proteostasis networkimmunityprotein aggregation

Identifiers

PMID42438074
PMCPMC13580247

What OpenQuestion holds

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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.