Li Shuang, Liu Dan, Fu Yuying, Zhang Chunyu, Tong Huili, Li Shufeng, Yan Yunqin
The Laboratory of Cell and Development, Northeast Agricultural University, Harbin, China.
Front Physiol. 2019 Aug 7;10:1010. doi: 10.3389/fphys.2019.01010. eCollection 2019.
Small leucine-rich repeat proteins (SLRPs) are highly effective and selective modulators of cell proliferation and differentiation. Podocan is a newly discovered member of the SLRP family. Its potential roles in the differentiation of bovine muscle-derived satellite cells (MDSCs) and its underlying functional mechanism remain unclear. Our study aimed to characterize the function of the podocan gene in the differentiation of bovine MDSCs and to clarify the molecular mechanism by which podocan functions in order to contribute to a better understanding of the molecular mechanism by which extracellular matrix promotes bovine MDSC differentiation and provide a theoretical basis for the improvement of beef quality.
Bovine MDSCs were transfected with vectors to overexpress or inhibit podocan, and podocan protein was added to differentiation culture medium. qRT-PCR, western blotting, and immunofluorescence were performed to investigate the effects of podocan on MDSC differentiation. Confocal microscopy and western blotting were used to assess the nuclear translocation and expression of β-catenin. An inhibitor and activator of β-catenin were used to assess the effects of the Wnt/β-catenin signaling pathway on MDSC differentiation. We inhibited β-catenin while overexpressing podocan in MDSCs. Then, we performed mass spectrometry to identify which proteins interact with podocan to regulate the Wnt/β-catenin signaling pathway. Finally, we confirmed the relationship between podocan and Wnt4 by co-immunoprecipitation and western blotting.
Podocan protein expression increased significantly during bovine MDSC differentiation. Differentiation of bovine MDSC was promoted and suppressed by podocan overexpression or inhibition, respectively. Podocan was also shown to modulate the Wnt/β-catenin signaling pathway. Treatment of bovine MDSCs with β-catenin inhibitor and activator showed that the Wnt/β-catenin pathway is involved in bovine MDSC differentiation. Furthermore, the effect of podocan on bovine MDSC differentiation was suppressed when this pathway was inhibited. We also found that podocan interacts with Wnt4. When Wnt4 was inhibited, podocan-induced promotion of bovine MDSC differentiation was attenuated through Wnt/β-catenin signaling.
Podocan regulates Wnt/β-catenin through Wnt4 to promote bovine MDSC differentiation.
富含亮氨酸的小分子重复蛋白(SLRPs)是细胞增殖和分化的高效且选择性调节剂。足蛋白聚糖是SLRP家族新发现的成员。其在牛肌肉来源卫星细胞(MDSCs)分化中的潜在作用及其潜在功能机制尚不清楚。我们的研究旨在表征足蛋白聚糖基因在牛MDSCs分化中的功能,并阐明足蛋白聚糖发挥作用的分子机制,以有助于更好地理解细胞外基质促进牛MDSCs分化的分子机制,并为改善牛肉品质提供理论依据。
用载体转染牛MDSCs以过表达或抑制足蛋白聚糖,并将足蛋白聚糖蛋白添加到分化培养基中。进行qRT-PCR、蛋白质印迹和免疫荧光以研究足蛋白聚糖对MDSCs分化的影响。使用共聚焦显微镜和蛋白质印迹评估β-连环蛋白的核转位和表达。使用β-连环蛋白抑制剂和激活剂评估Wnt/β-连环蛋白信号通路对MDSCs分化的影响。我们在MDSCs中抑制β-连环蛋白的同时过表达足蛋白聚糖。然后,我们进行质谱分析以鉴定哪些蛋白质与足蛋白聚糖相互作用以调节Wnt/β-连环蛋白信号通路。最后,我们通过免疫共沉淀和蛋白质印迹证实了足蛋白聚糖与Wnt4之间的关系。
在牛MDSCs分化过程中,足蛋白聚糖蛋白表达显著增加。足蛋白聚糖的过表达或抑制分别促进和抑制了牛MDSCs的分化。足蛋白聚糖还显示出调节Wnt/β-连环蛋白信号通路的作用。用β-连环蛋白抑制剂和激活剂处理牛MDSCs表明Wnt/β-连环蛋白通路参与牛MDSCs分化。此外,当该通路被抑制时,足蛋白聚糖对牛MDSCs分化的影响受到抑制。我们还发现足蛋白聚糖与Wnt4相互作用。当Wnt4被抑制时,足蛋白聚糖诱导的牛MDSCs分化促进作用通过Wnt/β-连环蛋白信号减弱。
足蛋白聚糖通过Wnt4调节Wnt/β-连环蛋白以促进牛MDSCs分化。