Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition
Objective To investigate the effect and underlying mechanism of galectin-3 (Gal-3) on the proliferation of mesangial cells (MCs) cultured under high glucose condition. Methods Real-time quantitative PCR (qRT-PCR) was used to detect the expression of Gal-3 in normal and diabetic nephropathy (DN) mous...
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Editorial Office of Journal of Third Military Medical University
2020-10-01
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doaj-fdea796e48f94687ba38b83b032beac12021-05-21T00:34:11ZzhoEditorial Office of Journal of Third Military Medical UniversityDi-san junyi daxue xuebao1000-54042020-10-0142191913191910.16016/j.1000-5404.202004076Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition LIN Ziyue0ZHANG Panyang1CHONG Xinyu2 Department of Cell Biology and Genetics, College of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, China Department of Cell Biology and Genetics, College of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, China Department of Cell Biology and Genetics, College of Basic Medical Sciences, Chongqing Medical University, Chongqing, 400016, ChinaObjective To investigate the effect and underlying mechanism of galectin-3 (Gal-3) on the proliferation of mesangial cells (MCs) cultured under high glucose condition. Methods Real-time quantitative PCR (qRT-PCR) was used to detect the expression of Gal-3 in normal and diabetic nephropathy (DN) mouse kidney tissues and MCs under low and high glucose conditions. Gal-3 overexpression plasmid and siRNA were constructed and synthesized. qRT-PCR and Western blotting were used to detect the transfection efficiency. And Gal-3 overexpression plasmid or siRNA was transfected into MCs under low and high glucose condition, respectively. Further, 5-Ethynyl-2′-deoxyuridine (EdU) was used to detect the cell proliferation ability, and Western blot assay was used to measure the expression of Mek and phosphorylated Mek after overexpression or downexpression of Gal-3 in MCs. Results qRT-PCR results showed that Gal-3 expression was significantly higher in the kidney tissues of DN mice than those of the normal mice(P < 0.01), and so was the expression level in MCs under high glucose condition when compared with the cells under low glucose condition (P < 0.01). In addition, overexpression of Gal-3 resulted in enhanced proliferation ability of MCs (P < 0.01) and the up-regulation of phosphorylated Mek (P < 0.01). While, Gal-3 silencing induced the opposite results in the proliferation ability (P < 0.01) and phosphorylated Mek expression (P < 0.001). Conclusion Gal-3 is significantly up-regulated in DN, and may affect the proliferation of MCs by regulating Mek phosphorylation, and thus plays an important regulatory role in DN.http://aammt.tmmu.edu.cn/Upload/rhtml/202004076.htmdiabetic nephropathygalectin-3glomerular mesangial cellsproliferationmek |
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DOAJ |
language |
zho |
format |
Article |
sources |
DOAJ |
author |
LIN Ziyue ZHANG Panyang CHONG Xinyu |
spellingShingle |
LIN Ziyue ZHANG Panyang CHONG Xinyu Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition Di-san junyi daxue xuebao diabetic nephropathy galectin-3 glomerular mesangial cells proliferation mek |
author_facet |
LIN Ziyue ZHANG Panyang CHONG Xinyu |
author_sort |
LIN Ziyue |
title |
Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition |
title_short |
Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition |
title_full |
Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition |
title_fullStr |
Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition |
title_full_unstemmed |
Galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition |
title_sort |
galectin-3 regulates proliferation of glomerular mesangial cells under high glucose condition |
publisher |
Editorial Office of Journal of Third Military Medical University |
series |
Di-san junyi daxue xuebao |
issn |
1000-5404 |
publishDate |
2020-10-01 |
description |
Objective To investigate the effect and underlying mechanism of galectin-3 (Gal-3) on the proliferation of mesangial cells (MCs) cultured under high glucose condition. Methods Real-time quantitative PCR (qRT-PCR) was used to detect the expression of Gal-3 in normal and diabetic nephropathy (DN) mouse kidney tissues and MCs under low and high glucose conditions. Gal-3 overexpression plasmid and siRNA were constructed and synthesized. qRT-PCR and Western blotting were used to detect the transfection efficiency. And Gal-3 overexpression plasmid or siRNA was transfected into MCs under low and high glucose condition, respectively. Further, 5-Ethynyl-2′-deoxyuridine (EdU) was used to detect the cell proliferation ability, and Western blot assay was used to measure the expression of Mek and phosphorylated Mek after overexpression or downexpression of Gal-3 in MCs. Results qRT-PCR results showed that Gal-3 expression was significantly higher in the kidney tissues of DN mice than those of the normal mice(P < 0.01), and so was the expression level in MCs under high glucose condition when compared with the cells under low glucose condition (P < 0.01). In addition, overexpression of Gal-3 resulted in enhanced proliferation ability of MCs (P < 0.01) and the up-regulation of phosphorylated Mek (P < 0.01). While, Gal-3 silencing induced the opposite results in the proliferation ability (P < 0.01) and phosphorylated Mek expression (P < 0.001). Conclusion Gal-3 is significantly up-regulated in DN, and may affect the proliferation of MCs by regulating Mek phosphorylation, and thus plays an important regulatory role in DN. |
topic |
diabetic nephropathy galectin-3 glomerular mesangial cells proliferation mek |
url |
http://aammt.tmmu.edu.cn/Upload/rhtml/202004076.htm |
work_keys_str_mv |
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