Evidence map›Paper›PMID 42298696›Full record

ArticleJournal of orthopaedic surgery and research2026

Sequential vascular and neural changes underlying the progression of patellar tendinopathy.

Jinsung Park, Naoki Takemoto, Tae-Hwan Kim, Junsuke Nakase, Jin Kyu Lee

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Article in Journal of orthopaedic surgery and research, 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jinsung Park *Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.
Naoki Takemoto *Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Ishikawa, Japan.
Tae-Hwan KimHanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.
Junsuke NakaseDepartment of Orthopaedic Surgery, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Ishikawa, Japan. nakase1007@yahoo.co.jp.
Jin Kyu LeeHanyang University Institute for Rheumatology Research, Seoul, Republic of Korea. jklee77@hanyang.ac.kr.

Funding

Korean Fund for Regenerative Medicine RS-2023-00215515National Research Foundation of Korea 2021R1A6A1A03038899
6 · The paper itself

Abstract

purposeTo investigate the temporal sequence of vascular, neural, and extracellular matrix (ECM) changes during the progression of collagenase-induced patellar tendinopathy and to test the hypothesis that early angiogenesis initiates a cascade leading to neural remodeling and tendon degeneration.

methodsA collagenase-induced rat patellar tendinopathy model was established in 40 male Sprague-Dawley rats. Animals were divided into one control group (PBS injection, n = 8, sacrificed at 12 weeks) and four experimental groups (collagenase type I injection, n = 8 each, sacrificed at 2, 4, 8, and 12 weeks post-injection). Histological evaluation (H&E and Masson's trichrome staining), immunohistochemistry, immunofluorescence (CD31, α-SMA, CGRP), and RT-qPCR for Col1a1, Col3a1, decorin (Dcn), and tenascin C (Tnc) were performed. Semi-quantitative scoring of cellularity, fibrosis, and vascularity was applied. Statistical analysis was conducted using ANOVA.

resultsHistology revealed progressive hypercellularity, fibrosis, and calcification, with significant increases in cellularity from week 8 and in vascularity from week 4. Immunofluorescence showed CD31-positive cells increasing significantly at week 4, followed by α-SMA-positive and CGRP-positive cells at week 8. mRNA analysis demonstrated early peaks of Col3a1, Dcn, and Tnc expression at 2 weeks, while Col1a1 expression peaked at 8 weeks and declined sharply by week 12. The Col1a1/Col3a1 ratio was significantly elevated at 8 weeks before decreasing at 12 weeks.

conclusionThis study demonstrates a sequential progression in collagenase-induced patellar tendinopathy, where early angiogenesis precedes neural remodeling and ECM turnover. These findings suggest that vascular remodeling may be associated with subsequent neural and structural changes during tendinopathy progression.

Indexed as

Disease ProgressionNeovascularization, PathologicPatellar LigamentTendinopathyActinsAnimalsCollagenasesCollagen Type ICollagen Type I, alpha 1 ChainCollagen Type IIIDecorinExtracellular MatrixMaleRatsRats, Sprague-DawleyTenascinActa2 protein, ratActinsCOL3A1 protein, ratCollagenasesCollagen Type ICollagen Type I, alpha 1 ChainCollagen Type IIIDecorinTenascinAngiogenesisCollagenase-induced tendinopathy modelNeural remodeling (CGRP)Patellar tendinopathy

Identifiers

PMID42298696
PMCPMC13523466

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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.