Cellular Components and Their Correlations in the Subchondral Bone Plate and Cancellous Bone of Patients With Knee Osteoarthritis
Year: 2026
Type: article
Study design: Observational Study
Abstract: Objective: The load-bearing structures of the subchondral bone undergo alterations in osteoarthritis (OA) joints and exhibit distinct bone remodelling properties. This study examined the pathological features and cellular components of the subchondral bone plate (SCBP) and subchondral cancellous bone (SCCB) in OA-affected regions of human knee joints. Methods: Tibial plateaus were obtained from patients with varus knee OA (n = 42; women: n = 22, aged 57–87 years; men: n = 20, aged 59–82 years). Osteochondral specimens were collected from OA lesion sites in the medial compartment (OA region) and paired control sites in the lateral compartment (C region). Bone mineral density (BMD) was evaluated using micro-computed tomography, osterix+ osteoprogenitors, cathepsin K (CTSK)+ osteoclasts, and F4/80+ macrophages were quantified by immunohistochemistry, and correlations between cellular components were analysed by sex and region. Results: The OA SCBP had a significantly higher BMD than did the C region. In male patients, more F4/80+ macrophages were present in the SCBP C region than in the OA region. Female OA SCCB samples showed an increased number of CTSK+ osteoclasts. In both sexes, compared with the C region, the OA SCCB contained more CTSK+ osteoclasts and macrophages. Positive correlations between macrophage and osteoprogenitor densities were observed in most subchondral bone regions, except in male OA samples. Conclusions: Region-specific differences in cellular components were identified in the OA subchondral bone. Asynchronous remodelling responses were noted between the SCBP and SCCB. These findings provide detailed insights into OA pathology and can inform future therapeutic strategies.
Source: European Cells and Materials
DOI: 10.22203/ecm.v056a03
Language: English
Subfield: Rheumatology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,000
OpenAlex ID: W7160024410
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