Evidence map›Paper›PMID 41096604›Full record

ArticleInternational journal of molecular sciences2025

Localisation-Dependent Variations in Articular Cartilage ECM: Implications for Tissue Engineering and Cartilage Repair.

Laura Weimer, Luisa M Schmidt, Gerhard Sengle, Marcus Krüger, Alan M Smith, Ilona Brändlin, Frank Zaucke

Erratum issuedAbstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Laura WeimerFaculty 2: Computer Science and Engineering, Frankfurt University of Applied Sciences, 60318 Frankfurt, Germany.
Luisa M SchmidtInstitute for Genetics, Cologne Excellence Cluster on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), and Center for Molecular Medicine Cologne (CMMC), University of Cologne, 50931 Cologne, Germany.ORCID 0000-0002-9805-4941
Gerhard SengleDepartment of Pediatrics and Adolescent Medicine, Faculty of Medicine and University Hospital Cologne, Center for Biochemistry, Center for Molecular Medicine Cologne (CMMC), Cologne Center for Musculoskeletal Biomechanics (CCMB), and Cologne Excellence Cluster on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.
Marcus KrügerInstitute for Genetics, Cologne Excellence Cluster on Cellular Stress Responses in Ageing-Associated Diseases (CECAD), and Center for Molecular Medicine Cologne (CMMC), University of Cologne, 50931 Cologne, Germany.ORCID 0000-0002-5846-6941
Alan M SmithDepartment of Pharmacy, School of Applied Sciences, University of Huddersfield, Huddersfield HD1 3DH, UK.ORCID 0000-0003-2791-3208
Ilona BrändlinFaculty 2: Computer Science and Engineering, Frankfurt University of Applied Sciences, 60318 Frankfurt, Germany.
Frank ZauckeDr. Rolf M. Schwiete Osteoarthritis Research Unit, Department of Trauma Surgery and Orthopedics, University Hospital, Goethe University, 60528 Frankfurt, Germany.ORCID 0000-0002-7680-9354

Funding

B. Braun Foundation BBST-D-23-00139Deutsche Forschungsgemeinschaft 384170921, FOR2722, KR3788/8-2Deutsche Forschungsgemeinschaft 384170921, FOR2722, ZA561/3-2Deutsche Forschungsgemeinschaft 397484323 TRR259Deutsche Forschungsgemeinschaft 468236352
6 · The paper itself

Abstract

Articular cartilage (AC) is a specialised connective tissue covering joint surfaces. It enables smooth movement, distributes mechanical loads, and protects the underlying bone. In response to loading, AC adapts by modifying both its thickness and composition. AC is organised in different zones, with low cellularity and a high abundance of extracellular matrix (ECM). Mechanical overloading or immobilisation can lead to structural changes, potentially resulting in osteoarthritis (OA), for which no causal treatment currently exists. However, smaller defects can be treated using chondrocyte/cartilage transplantation or tissue engineering. A better understanding of the molecular composition of AC at different locations is essential to improve such therapeutic approaches. For this purpose, we performed a comprehensive analysis of porcine femoral knee cartilage at eight defined anatomical sites. Cartilage thickness and proteoglycan (PG) content were analysed histologically, while specific ECM proteins were assessed by proteomics and validated by immunohistochemistry and Western blot. Significant differences were identified, particularly between medial and lateral compartments, in terms of cartilage thickness, PG abundance, and ECM composition. Some proteins also showed zone-specific localisation patterns. These structural differences likely reflect adaptation to mechanical loading and should be considered to optimise future cartilage repair and tissue engineering strategies.

Indexed as

Cartilage, ArticularExtracellular MatrixTissue EngineeringAnimalsBlotting, WesternExtracellular Matrix ProteinsImmunohistochemistryProteoglycansProteomicsSwineExtracellular Matrix ProteinsProteoglycansarticular cartilagecollagenextracellular matrixproteoglycanproteomics

Identifiers

PMID41096604
PMCPMC12524475

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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.