在使用 RPTEC/TERT1 细胞系的肾脏纤维化体外模型中,BMSC 调节培养基的治疗潜力。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-02-01
Yunji Kim, Dayeon Kang, Ga-Eun Choi, Sang Dae Kim, Sun-Ja Yang, Hyosang Kim, Dalsan You, Choung Soo Kim, Nayoung Suh
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引用次数: 0

摘要

我们研究了骨髓间充质干细胞调节培养基(BMSC-CM)在纤维化环境中对永生化肾近曲小管上皮细胞(RPTEC/ TERT1)的治疗潜力。为了复制慢性肾病患者肾脏特有的硬度增加现象,我们使用了聚丙烯酰胺凝胶平台。结果表明,僵硬的基质会增加α-平滑肌肌动蛋白(α-SMA)的水平,这表明RPTEC/TERT1细胞发生了纤维化活化。有趣的是,用 BMSC-CM 处理后,纤维化标记物(α-SMA 和波形蛋白)的水平明显降低,而上皮标记物 E-cadherin 和 aquaporin 7 的水平则升高,尤其是在僵硬条件下。此外,BMSC-CM 还能改变微核糖核酸(miRNA)的表达,降低这些细胞的氧化应激水平。我们的研究结果表明,BMSC-CM 可调节 RPTEC/TERT1 细胞的细胞形态、miRNA 表达和氧化应激,突出了其在纤维化肾病中的治疗潜力。
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Therapeutic potential of BMSC-conditioned medium in an in vitro model of renal fibrosis using the RPTEC/TERT1 cell line.

We investigated the therapeutic potential of bone marrow-derived mesenchymal stem cell-conditioned medium (BMSC-CM) on immortalized renal proximal tubule epithelial cells (RPTEC/ TERT1) in a fibrotic environment. To replicate the increased stiffness characteristic of kidneys in chronic kidney disease, we utilized polyacrylamide gel platforms. A stiff matrix was shown to increase α-smooth muscle actin (α-SMA) levels, indicating fibrogenic activation in RPTEC/TERT1 cells. Interestingly, treatment with BMSC-CM resulted in significant reductions in the levels of fibrotic markers (α-SMA and vimentin) and increases in the levels of the epithelial marker E-cadherin and aquaporin 7, particularly under stiff conditions. Furthermore, BMSC-CM modified microRNA (miRNA) expression and reduced oxidative stress levels in these cells. Our findings suggest that BMSC-CM can modulate cellular morphology, miRNA expression, and oxidative stress in RPTEC/TERT1 cells, highlighting its therapeutic potential in fibrotic kidney disease. [BMB Reports 2024; 57(2): 116-121].

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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