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骨髓间充质基质细胞分泌因子和细胞外囊泡可调节免疫和组织再生,用于骨关节炎治疗。

Secreted Factors and Extracellular Vesicles Account for the Immunomodulatory and Tissue Regenerative Properties of Bone-Marrow-Derived Mesenchymal Stromal Cells for Osteoarthritis.

机构信息

Laboratorio di Biotecnologie Applicate all'Ortopedia, IRCCS Istituto Ortopedico Galeazzi, Via R. Galeazzi 4, I-20161 Milan, Italy.

出版信息

Cells. 2022 Nov 4;11(21):3501. doi: 10.3390/cells11213501.

Abstract

Bone-marrow-derived mesenchymal stromal cells (BMSCs) showed therapeutic potential in the treatment of musculoskeletal diseases, including osteoarthritis (OA). Their soluble mediators and extracellular vesicles (EVs), which make up the secretome, suppress immune response, attenuate inflammation and promote cartilage repair. EVs, as well as the whole secretome, have been investigated as cell free approaches for OA although, to date, a disease-tailored molecular fingerprint is missing. In this study, soluble mediators and miRNAs were sifted in the BMSCs' secretome and EVs, respectively, and analyzed in the frame of cell types and factors involved in OA. The majority of identified molecules repress the activation of immune cells and the production of OA-related inflammatory mediators, as well as promote cartilage protection by acting on both chondrocytes homeostasis and extracellular matrix-degrading enzymes. These data provide the molecular ground for the therapeutic potential of BMSCs for regenerative applications for OA and support the use of secretome or EVs as cell-free applications in joint diseases.

摘要

骨髓间充质基质细胞 (BMSCs) 在治疗肌肉骨骼疾病方面表现出了治疗潜力,包括骨关节炎 (OA)。它们的可溶性介质和细胞外囊泡 (EVs) 构成了分泌组,能够抑制免疫反应、减轻炎症并促进软骨修复。EVs 和整个分泌组都被研究为 OA 的无细胞治疗方法,尽管迄今为止,针对 OA 的定制分子指纹图谱仍缺乏。在这项研究中,分别筛选了 BMSCs 分泌组中的可溶性介质和 miRNA,并在涉及 OA 的细胞类型和因子的框架内进行了分析。鉴定出的大多数分子可抑制免疫细胞的激活和 OA 相关炎症介质的产生,同时通过作用于软骨细胞稳态和细胞外基质降解酶来促进软骨保护。这些数据为 BMSCs 用于 OA 再生应用的治疗潜力提供了分子基础,并支持将分泌组或 EVs 用作关节疾病的无细胞治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9538/9658264/2b614d213e65/cells-11-03501-g001.jpg

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