不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Mesenchymal Stem Cell Exosomal miR-146a Mediates the Regulation of the TLR4/MyD88/NF-κB Signaling Pathway in Inflammation due to Diabetic Retinopathy.
Mesenchymal Stem Cell Exosomal miR-146a Mediates the Regulation of the TLR4/MyD88/NF-κB Signaling Pathway in Inflammation due to Diabetic Retinopathy.
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糖尿病视网膜病变(DR)是糖尿病患者视力丧失的主要原因,单纯控制血糖无法完全解决。炎症会影响DR发展,因此减轻患者炎症反应对于预防DR至关重要。
本研究探讨骨髓间充质干细胞(BMSC)外泌体对DR小鼠炎症的调节作用。为分析作用机制,研究使用BMSC外泌体miR-146a处理DR小鼠小胶质细胞,观察细胞变化和炎症因子表达。结果发现,BMSC外泌体miR-146a降低DR小鼠小胶质细胞中的增殖细胞抗原和B细胞淋巴瘤2水平,并提高Bcl-2相关X蛋白及半胱天冬酶3水平。炎症因子分析显示,BMSC外泌体miR-146a降低TNF-α、IL-1β和IL-6水平,提示miR-146a可减轻DR小鼠炎症。
进一步研究发现,miR-146a降低TLR4活性并提高MyD88和NF-κB活性。过表达TLR4可逆转miR-146a对小胶质细胞增殖、凋亡和炎症的影响。
本研究表明,BMSC外泌体miR-146a可通过调节TLR4/MyD88/NF-κB信号通路控制DR炎症反应,为DR预防和治疗提供实验依据。
Diabetic retinopathy (DR) is the main cause of vision loss in diabetic patients, which cannot be completely resolved by typical blood sugar control. Inflammation influences the development of DR, so reducing the inflammatory response in DR patients is crucial to the prevention of DR.
Therefore, we explored the regulatory effect of bone marrow mesenchymal stem cell (BMSC) exosomes on inflammation in DR mice. In order to analyze the mechanism of action, we used BMSC exosomal miR-146a to treat microglias in DR mice to observe cellular changes and expression of inflammatory factors.
It was found that BMSC exosomal miR-146a reduced the levels of proliferating cell antigen and B-cell lymphoma-2 in microglias of DR mice and increased Bcl-2-related X with cysteine aspartic protease-3. By analyzing the expression of inflammatory factors, we found that BMSC exosomal miR-146a reduced the levels of TNF- , IL-1 , and IL-6, which suggested that miR-146a can alleviate inflammation in DR mice.
Further exploration found that miR-146a reduced the activity of TLR4 and increased the activity of MyD88 and NF- B.
Furthermore, the overexpression of TLR4 reversed the effects of miR-146a on the proliferation, apoptosis, and inflammation of microglias.
Our study demonstrated that BMSC exosomal miR-146a can regulate the inflammatory response of DR by mediating the TLR4/MyD88/NF- B pathway, providing an experimental basis for the prevention and treatment of DR.
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