Evidence map›Paper›PMID 35882934›Full record

ArticleNature immunology2022

Lymph node homeostasis and adaptation to immune challenge resolved by fibroblast network mechanics.

Harry L Horsnell, Robert J Tetley, Henry De Belly, Spyridon Makris, Lindsey J Millward, Agnesska C Benjamin, Lucas A Heeringa, Charlotte M de Winde, Ewa K Paluch, Yanlan Mao and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Nature immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
7.0field-weighted citation impact, top 2% of its field
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

44 citing papers in PubMed, 61 citations in OpenAlex.

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  13. Antigen mobility regulates the dynamics and precision of antigen capture in the B cell immune synapse.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  19. Fibroblasts in heterotopic ossification: mechanisms and therapeutic targets.International journal of biological sciences · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Harry L HorsnellStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.ORCID 0000-0002-4321-6958
Robert J TetleyTissue Mechanics Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Henry De BellyPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Spyridon MakrisStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Lindsey J MillwardStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Agnesska C BenjaminStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Lucas A HeeringaStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Charlotte M de WindeStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Ewa K PaluchPhysiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Yanlan MaoTissue Mechanics Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK.
Sophie E ActonStromal Immunology Group, MRC Laboratory for Molecular Cell Biology, University College London, London, UK. s.acton@ucl.ac.uk.ORCID 0000-0003-2704-716X
MRC Laboratory for Molecular Cell Biology · GBUniversity of Cambridge · GB

Funding

Cancer Research UK 19763Cancer Research UK A19763Cancer Research UK CRUK-A19763Medical Research Council MC-U12266BMedical Research Council MC_UP_1205/1Medical Research Council MC_UU_00012/5Medical Research Council MC_UU_12018/5Medical Research Council MR/L009056/Medical Research Council MR/L009056/1Medical Research Council MR/T031646/1Medical Research Council MR/W027437/1
6 · The paper itself

Abstract

Emergent physical properties of tissues are not readily understood by reductionist studies of their constituent cells. Here, we show molecular signals controlling cellular, physical, and structural properties and collectively determine tissue mechanics of lymph nodes, an immunologically relevant adult tissue. Lymph nodes paradoxically maintain robust tissue architecture in homeostasis yet are continually poised for extensive expansion upon immune challenge. We find that in murine models of immune challenge, cytoskeletal mechanics of a cellular meshwork of fibroblasts determine tissue tension independently of extracellular matrix scaffolds. We determine that C-type lectin-like receptor 2 (CLEC-2)-podoplanin signaling regulates the cell surface mechanics of fibroblasts, providing a mechanically sensitive pathway to regulate lymph node remodeling. Perturbation of fibroblast mechanics through genetic deletion of podoplanin attenuates T cell activation. We find that increased tissue tension through the fibroblastic stromal meshwork is required to trigger the initiation of fibroblast proliferation and restore homeostatic cellular ratios and tissue structure through lymph node expansion.

Indexed as

FibroblastsLymph NodesAnimalsExtracellular MatrixHomeostasisLectins, C-TypeMiceLectins, C-Type

Identifiers

PMID35882934
PMCPMC9355877
OpenAlexW4288068964

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.