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4D bioprinting is a cutting-edge approach for manufacturing active scaffolds able to shape-morph in a predefined way after the application of an environmental stimulus, thus enabling to mimic the dynamics of native tissues. In this study, we developed a self-folding gelatin-based bilayer scaffold for trachea engineering exploiting the 4D bioprinting approach. Starting from a 2D flat configuration, upon hydration, the scaffold automatically forms a closed tubular structure. An analytical model, based on Timoshenko's beam thermostats, was developed and validated to predict the radius of curvature of the scaffold. The 4D bioprinted structure was tested with airway fibroblast, lung endothelial cells and cartilage progenitor cells (CPCs) toward the development of a tissue engineered trachea. Cells were seeded on the scaffold in its initial flat configuration, maintained their position after the scaffold actuation and proliferated over or inside it. The ability of CPCs to differentiate towards mature cartilage was evaluated. Interestingly, real-time PCR revealed that differentiating CPCs on the 4D bioprinted scaffold promotes healthier cartilage formation, if compared with CPCs cultured on 2D static flat scaffold. Thus, CPCs can perceive scaffold folding and its final curvature and react to it, towards the formation of mature cartilage for the airway.
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http://dx.doi.org/10.1002/admt.202401210 | DOI Listing |
ACS Synth Biol
September 2025
The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, P. R. China.
Human Bone Morphogenetic Protein-2 (hBMP-2) serves as a critical regulator in bone and cartilage formation; however, its industrial application is hindered by its inherent tendency to form inclusion bodies in prokaryotic expression systems. To address this issue, we established a recombinant hBMP-2 (rhBMP-2) expression system using the pCold II plasmid and the SHuffle T7 strain. We explored several strategies to enhance the solubility of rhBMP-2, including coexpression with molecular chaperones, vesicle-mediated secretory expression, fusion expression with synthetic intrinsically disordered proteins (SynIDPs), and fusion expression with small-molecule peptide tags.
View Article and Find Full Text PDFVet Surg
September 2025
Clinic for Small Animals, University of Veterinary Medicine Hannover, Hannover, Germany.
Objective: To describe and compare arthroscopy-assisted (AA) with fluoroscopy-assisted (FA) minimally invasive plate osteosynthesis (MIPO) for simple transverse acetabular fractures.
Study Design: Ex vivo cadaveric study.
Sample Population: A total of 10 canine cadavers (>20 kg) without coxofemoral joint disease.
Comp Biochem Physiol C Toxicol Pharmacol
September 2025
Department of Biotechnology, Bharathiar University, Coimbatore, Tamil Nadu, India. Electronic address:
Excessive fluoride (F) exposure, particularly during early development, poses a significant risk to skeletal integrity by disrupting bone homeostasis through oxidative stress and altered mineralization. While F induced oxidative stress is well documented, studies investigating the role of natural antioxidants in mitigating F induced osteochondral toxicity remains limited. Hence, the present study investigated the osteomodulatory effect of fisetin (Fis) against F toxicity in zebrafish larvae.
View Article and Find Full Text PDFJ Extracell Vesicles
September 2025
Division of Sports Medicine and Adult Reconstructive Surgery, Department of Orthopedic Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, China.
Osteoarthritis (OA), the prevalent debilitating joint disorder, is accelerated by dysregulated intercellular crosstalk, yet the role of fibroblast-like synoviocyte (FLS)-derived extracellular vesicles and particles (EVPs) in disease progression remains to be elucidated. Here, integrative analysis of clinical specimens, animal models, and publicly available datasets revealed significant alterations in exosomal pathways within OA synovium. Proteomic profiling revealed distinct molecular signatures in EVPs derived from inflammatory and senescent FLSs, reflecting the pathophysiological status of their parent cells.
View Article and Find Full Text PDFJ Orthop Translat
November 2025
Key Laboratory of Tropical Translational Medicine of Ministry of Education & Key Laboratory of Brain Science Research and Transformation in Tropical Environment of Hainan Province, Hainan Provincial Stem Cell Research Institute, School of Basic Medicine and Life Sciences, Hainan Medical University,
Unlabelled: Osteoarthritis (OA) is characterized by the inability of stable and complex joint structures to function as they did, accompanied by inflammation, tissue changes, chronic pain, and neuropathic inflammation. In the past, the primary focus on the causes of joint dysfunction has been on mechanical stress leading to cartilage wear. Further researches emphasize the aging of cartilage and subchondral bone triggered cartilage lesion and osteophyte formation.
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