MMP3型
椎间盘
基质金属蛋白酶
MMP2型
细胞外基质
流式细胞术
基质金属蛋白酶3
变性(医学)
病理
医学
癌症研究
细胞生物学
生物
下调和上调
基因表达
解剖
免疫学
基因
内科学
遗传学
作者
Qingxin Song,Fan Zhang,Kun Wang,Zhi Chen,Quan Li,Zude Liu,Hongxing Shen
标识
DOI:10.1016/j.ejphar.2021.173891
摘要
Intervertebral disc degeneration (IDD) is a spinal degenerative disease and one of the most important causes of musculoskeletal disability. Matrix metalloproteinase (MMP)-mediated extracellular matrix degradation is the core process of IDD. The regulators of MMPs in the intervertebral disc are still not fully known. In this study, using quantitative reverse transcription PCR, luciferase reporter assay, Western blotting, immunofluorescence, flow cytometry, and Cell Counting Kit-8 assay, we found that the miR-874-3p expression level was significantly decreased in IDD patients. MiR-874-3p could target and repress MMP2 and MMP3 expression in nucleus pulposus cells. These results could improve the understanding of IDD and provide a possible diagnostic marker and treatment candidate for IDD. The miR-874-3p/MMP2/MMP3 axis might also provide direction for future cancer and inflammation investigations.
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