Evidence map›Paper›PMID 41524834›Full record

ArticleTissue engineering and regenerative medicine2026

High-Concentration Type I Atelocollagen Enhances Early Cartilage Regeneration: An In Vivo Comparative Study.

Bo Seung Bae, Seon Ae Kim, Eun Jeong Go, Jae Woong Jung, Mi-La Cho, Asode Ananthram Shetty, Seok Jung Kim

Abstract readComparative Study
In one paragraph

Article in Tissue engineering and regenerative medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Bo Seung BaeDepartment of Orthopedic Surgery, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271, Cheonbo-Ro, Uijeongbu-Si, Seoul, Gyeonggi-Do, Republic of Korea.
Seon Ae KimDepartment of Orthopedic Surgery, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271, Cheonbo-Ro, Uijeongbu-Si, Seoul, Gyeonggi-Do, Republic of Korea.
Eun Jeong GoDepartment of Orthopedic Surgery, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271, Cheonbo-Ro, Uijeongbu-Si, Seoul, Gyeonggi-Do, Republic of Korea.
Jae Woong JungDepartment of Orthopedic Surgery, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271, Cheonbo-Ro, Uijeongbu-Si, Seoul, Gyeonggi-Do, Republic of Korea.
Mi-La ChoDepartment of Pathology, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Asode Ananthram ShettyInstitute of Medical Sciences, Faculty of Health and Social Care, Canterbury Christ Church University, Canterbury, UK.
Seok Jung KimDepartment of Orthopedic Surgery, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271, Cheonbo-Ro, Uijeongbu-Si, Seoul, Gyeonggi-Do, Republic of Korea. peter@catholic.ac.kr.ORCID http://orcid.org/0000-0002-9116-8786

Funding

National Research Foundation of Korea RS-2022-NR071147National Research Foundation of Korea RS-2023-NR077015
6 · The paper itself

Abstract

backgroundType I atelocollagen is used to treat full-thickness chondral lesions. However, evidence on the concentration-dependent effects of atelocollagen-based scaffolds on chondrogenesis is lacking. This study aimed to evaluate the in vitro and in vivo chondrogenic potentials of low-, intermediate-, and high-concentration atelocollagen-based scaffolds in a rabbit model of osteochondral defects.

methodsHuman mesenchymal stem cells (hMSCs) were encapsulated in 3%, 6%, and 9% type I collagen gels to assess cell viability and chondrogenic differentiation in vitro. In vivo, full-thickness osteochondral defects (4 × 4 mm) were created in 24 rabbits and treated as follows: Group 1 (microfracture only), Group 2 (microfracture + 3% atelocollagen), Group 3 (microfracture + 6%), and Group 4 (microfracture + 9%). The animals were euthanized at 4, 8, or 12 weeks. Macroscopic and histological outcomes were evaluated using gross morphological assessment and modified O'Driscoll scores.

resultsAt 8 weeks postoperatively, Group 4 (7.17 ± 0.76) exhibited significantly higher macroscopic scores than Group 2 (3.83 ± 0.29, p < 0.001) and Group 3 (4.50 ± 0.50, p < 0.001), indicating near-complete defect filling and smooth surface restoration. At 12 weeks, Groups 2 (7.33 ± 0.58), 3 (7.50 ± 0.87), and 4 (8.00 ± 0.00) all demonstrated significantly higher macroscopic scores than Group 1 (0.17 ± 0.12, p < 0.001 for all). Histologically, all atelocollagen-treated groups (Group 2:20.77 ± 1.55; Group 3:23.5 ± 1.00; Group 4:23.67 ± 1.44) exhibited significantly higher scores than Group 1 (1.67 ± 0.29, p < 0.001), with Group 4 achieving the highest overall.

conclusionHigh-concentration atelocollagen-based scaffolds significantly enhanced both the efficiency and quality of cartilage regeneration by providing mechanical support and a favorable microenvironment for chondrogenesis.

Indexed as

CartilageCartilage, ArticularCollagenCollagen Type IRegenerationAnimalsCell DifferentiationChondrogenesisHumansMesenchymal Stem CellsRabbitsTissue ScaffoldsatelocollagenCollagenCollagen Type IAtelocollagenChondrogenesisMesenchymal stem cell

Identifiers

PMID41524834
PMCPMC13031566

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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.