Evidence map›Paper›PMID 42039479›Full record

ArticlebioRxiv : the preprint server for biology2026

Expansion Microscopy reveals changes in cellular and extracellular structures between healthy and perturbed tendons.

Marcus A Woodworth, Tristan McDonnell, Xi Jiang, Zizhao Li, Yuna Heo, Mary Kate Evans, Robert L Mauck, Su Chin Heo, Nathaniel Dyment, Melike Lakadamyali

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

10 authors.

Marcus A WoodworthDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Tristan McDonnellCellular and Molecular Biology Program, Department of Biology, San Diego State University, San Diego, CA, United States.
Xi JiangMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.
Zizhao LiMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.
Yuna HeoMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.
Mary Kate EvansMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.
Robert L MauckMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.
Su Chin HeoMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.
Nathaniel DymentMcKay Orthopaedic Research Laboratory, Department of Orthopaedic Surgery, University of Pennsylvania, Philadelphia, PA, United States.ORCID 0000-0001-8708-112X
Melike LakadamyaliDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Funding

Research Project 2P50AR080581 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI LOUIS J SOSLOWSKY · 2023 to 2026
$7.9M
Integrative mechanisms of organelle dynamics from the atomic-to-cellular levelRM1GM136511 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI DOMINGUEZ, ROBERTO, HOLZBAUR, ERIKA L · 2020 to 2024
$7.4M
Training in Muscle Biology and Muscle DiseaseT32AR053461 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI OSTAP, E. MICHAEL · 2006 to 2025
$4.9M
Preserving chromatin nano-structure to enhance chondrocyte therapeutic potential for cartilage repairR01AR079224 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Su Chin Heo, Melike Lakadamyali · 2022 to 2026
$2.0M
Quantitative super-resolution imaging to map the multi-scale functional organization of cellsR35GM152111 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Melike Lakadamyali · 2024 to 2026
$1.7M
Calibration nanotemplates as universal standards for determining protein copy number in super-resolution microscopyR01GM133842 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LAKADAMYALI, MELIKE · 2019 to 2022
$1.7M
NIAMS NIH HHS P50 AR080581NIAMS NIH HHS R01 AR079224NIAMS NIH HHS T32 AR053461NIGMS NIH HHS R01 GM133842NIGMS NIH HHS R35 GM152111NIGMS NIH HHS RM1 GM136511
6 · The paper itself

Abstract

Tendons transmit mechanical forces between muscles and bones through their highly aligned, collagen-rich extracellular matrix. When damaged, resident cells help restore this matrix. However, in tendinopathies, this repair response fails, leading to loss of proper tendon function. How altered mechanical states reshape tendon cell and matrix architecture remains poorly understood because existing methods do not readily capture tendon structure across relevant length scales. Here, we combine Fluorescent Labeling of Abundant Reactive Entities (FLARE) with Expansion Microscopy (ExM) to visualize cellular and extracellular structures in native tendon tissue. FLARE-ExM resolves the dense fibrillar matrix across multiple tendon types, including elastic fibers and glycan-rich cellular protrusions. In a tendon resection model, acute loss-of-tension was associated with increased fibril width and expansion of carbohydrate- and protein-rich regions. In ruptured human Achilles tendon, FLARE-ExM revealed extracellular disorganization and disrupted cellular architecture. These results establish FLARE-ExM as a useful approach for studying how mechanical perturbation remodels tendon architecture across physiological and disease contexts.

Identifiers

PMID42039479
PMCPMC13104912

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LicenceCC BY-NC
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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.