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To regenerate a functional engineered cartilage in vitro with favorable mechanical property remains a bottleneck problem. The mechanical properties are known mainly determined by the unique extracellular matrix structure. Because of the limited detection methods, this study applied proteomics analysis to fully elucidate protein profiles that related to the mechanical property between in vitro and in vivo engineered cartilages. Passage 1 chondrocytes were used for in vitro cartilage engineering for 4 weeks. Then the constructs were kept in culture in vitro or implanted subcutaneously into nude mice for another 6 weeks. The engineered neo-cartilages were subjected to proteomic analysis, histologic examination, quantitation of glycosaminoglycan, Young Modulus, and transmission electron microscope observation. As expected, the engineered cartilages in vivo exhibited a more mature tissue characterized by a firmer tissue texture and densely deposited matrices than the in vitro group. Proteomic analysis showed that total 387 proteins were identified from both groups with 75 and 95 proteins uniquely presented in in vivo and in vitro groups, respectively. The differentially expressed proteins could generally be classified into the categories of extracellular matrix, structural molecules, cellular process, physiological process, cell and binding proteins. Proteomic analysis of selected molecules had partially revealed the proteins associated with the mechanical properties of the engineered cartilages. This study revealed a certain of important proteins associated with the mechanical properties in the maturation of engineered cartilages using mass spectrometry along with shotgun strategy.
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http://dx.doi.org/10.1097/SCS.0000000000011034 | DOI Listing |
Arch Toxicol
September 2025
Laboratorio de Proteómica, Facultad de Microbiología, Instituto Clodomiro Picado, Universidad de Costa Rica, San José, 11501, Costa Rica.
The scorpion Hottentotta judaicus inhabits the Levant region of the Middle East, including Lebanon, Jordan, Palestine, and Israel. While previous research focused on its insecticidal properties and sodium-channel-targeting toxins, its venom remains largely unexplored using modern proteomic approaches. We analyzed the venom composition of H.
View Article and Find Full Text PDFInt J Surg
September 2025
Department of Urology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Background: The pathophysiological changes driving incident kidney cancer remain unclear. This study aimed to identify protein biomarkers and underlying mechanisms using pre-diagnostic plasma proteomics.
Materials And Methods: Among 48,851 UK Biobank participants, 165 were diagnosed with kidney cancer, and 2,911 plasma proteins were analyzed.
J Periodontal Res
September 2025
Department of Biomaterials, Institute of Clinical Dentistry, University of Oslo, Oslo, Norway.
Aims: To compare the early wound-healing responses to crosslinked hyaluronic acid enriched with two proline-rich peptides (P2, P6) against unmodified hyaluronic acid and the enamel-matrix derivative (EMD) in a porcine gingival-detachment model.
Methods: In six pigs, defects around premolars were treated with HA, HA + P2, HA + P6 or EMD. After 6 days, the sites were harvested and evaluated using histology, immunohistochemistry, multiplex cytokine assay and untargeted proteomics of the gels, which were examined, informing an integrated multiomics approach analysis.
Arthritis Rheumatol
August 2025
Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Objective: To evaluate dynamic changes in autoantibody and proteomic profiles in treatment-naïve systemic sclerosis (SSc) patients and identify biomarkers and mechanisms associated with disease progression.
Methods: Serum samples from 30 baseline and 49 follow-up SSc patients, along with 38 controls, were analyzed. Autoantibody profiles were assessed using an autoantigen microarray targeting 120 autoantibodies, while proteomic analysis was conducted via liquid chromatography-mass spectrometry in data-independent acquisition mode.
J Proteome Res
September 2025
Department of Gastroenterology and Hepatology, West China Hospital, Sichuan University, Chengdu 610041, China.
Colorectal cancer (CRC) is a major global health challenge due to its high incidence, mortality, and low rate of early detection. Early diagnosis, targeting precancerous lesions (advanced adenomas) and early stage CRC (Tis and T1), is critical for improving patient survival. Given the limitations of current detection methods for advanced adenomas, developing high-performance early diagnostic strategies is essential for effective prevention.
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