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Investigating the mechanobiology of chondrocytes is challenging due to the complex micromechanical environment of cartilage tissue. The innate zonal differences and poroelastic properties of the tissue combined with its heterogeneous composition create spatial- and temporal-dependent cell behavior, which further complicates the investigation. Despite the numerous challenges, understanding the mechanobiology of chondrocytes is crucial for developing strategies for treating cartilage related diseases as chondrocytes are the only cell type within the tissue. The effort to understand chondrocyte behavior under various mechanical stimuli has been ongoing over the last 50 years. Early studies examined global biosynthetic behavior under unidirectional mechanical stimulus. With the technological development in high-speed confocal imaging techniques, recent studies have focused on investigating real-time individual and collective cell responses to multiple / combined modes of mechanical stimuli. Such efforts have led to tremendous advances in understanding the influence of local physical stimuli on chondrocyte behavior. In addition, we highlight the wide variety of experimental techniques, spanning from static to impact loading, and analysis techniques, from biochemical assays to machine learning, that have been utilized to study chondrocyte behavior. Finally, we review the progression of hypotheses about chondrocyte mechanobiology and provide a perspective on the future outlook of chondrocyte mechanobiology.
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http://dx.doi.org/10.1007/978-3-031-25588-5_2 | DOI Listing |
Osteoarthritis Cartilage
September 2025
Department of Inflammation and Ageing, School of Infection, Inflammation and Immunology, College of Medicine and Health, University of Birmingham, Birmingham B15 2TT, United Kingdom; National Institute for Health and Care Research (NIHR) Birmingham Biomedical Research Centre, United Kingdom. Electro
Objective: To investigate the inflammatory profiles of adipose tissues from patients with osteoarthritis (OA), comparing the joint-associated adipose tissues (infrapatellar fat pad (IFP) and sub-synovial (SSAT)) with subcutaneous adipose tissue (SCAT), and to explore adipose-joint cell crosstalk.
Design: RNA sequencing was performed on autologous IFP, SSAT, and SCAT from six patients. The adipose tissue secretome was profiled using targeted proteomics.
Mater Today Bio
October 2025
Department of Facial Plastic and Reconstructive Surgery, Eye and ENT Hospital, Fudan University, Shanghai, China.
Cartilage defects, whether congenital or acquired, are highly prevalent in clinical practice. Tissue engineering offers a promising strategy for cartilage regeneration; however, the loss of chondrocyte phenotype during expansion remains a major barrier to the clinical translation of chondrocyte-based engineered cartilage. Emerging evidence has highlighted that alterations in chondrocyte metabolic states can profoundly impact their phenotypic stability.
View Article and Find Full Text PDFNat Commun
August 2025
Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC, USA.
Osteoarthritis affects millions worldwide, yet effective treatments remain elusive due to poorly understood molecular mechanisms. While genome-wide association studies (GWAS) have identified hundreds of osteoarthritis-associated loci, identifying the genes impacted at each locus remains challenging. We investigate alternative splicing using RNA-sequencing data from 101 human chondrocyte samples treated with phosphate-buffered saline or fibronectin fragment, an osteoarthritis trigger.
View Article and Find Full Text PDFClin Biomech (Bristol)
October 2025
Department of Spine Surgery, Tianjin Union Medical Center, The First Affiliated Hospital of Nankai University, Tianjin 300121, China. Electronic address:
Background: This study aimed to systematically investigate how different degrees of mechanical loading caused by varying varus angles affect stress distribution and chondrocyte apoptosis in the medial tibial plateau of the knee joint. Specifically, it integrates finite-element analysis to simulate biomechanical stress patterns and evaluates the molecular responses (Piezo1, Bax, Bcl-2, and caspase-3 expressions) to elucidate the mechanobiological interplay contributing to cartilage degeneration.
Methods: Four knee models with varus angles (6°, 9°, 12°, and 15°) were constructed from computed tomography images.
Int J Mol Sci
August 2025
Department of Medicine for Sports and Performing Arts, Graduate School of Medicine, The University of Osaka, Osaka 565-0871, Japan.
Osteoarthritis (OA) is the most common joint disorder worldwide. Autologous chondrocyte implantation (ACI) is an established treatment for articular cartilage defects of the knee, but its effectiveness in OA is still under investigation. In this study, we investigated the effects of a newly developed mammalian-derived collagen matrix, NC-Col, on the proliferation, migration, adhesion, and gene expression of human articular cartilage-derived chondrocytes from OA patients in vitro, using proliferation assays, wound healing assays, adhesion assays, RT-qPCR, and RNA sequencing, respectively.
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