Suppr超能文献

凝集素 Orysata 诱导昆虫细胞的磷酸酶介导和碳水化合物非依赖性聚集。

The lectin Orysata induces phosphatase-mediated and carbohydrate-independent aggregation of insect cells.

机构信息

Department of Plants and Crops, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium; Department of Biotechnology, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium.

Department of Plants and Crops, Faculty of Bioscience Engineering, Ghent University, 9000 Ghent, Belgium.

出版信息

J Insect Physiol. 2021 May-Jun;131:104241. doi: 10.1016/j.jinsphys.2021.104241. Epub 2021 Apr 18.

Abstract

Lectins, or carbohydrate-binding proteins, can cause agglutination of particular cells. This process is mediated by the interaction of the carbohydrate-binding domain with sugar structures on the cell surface, and this binding can be inhibited by pre-incubation of the lectin with its specific sugars. However, when incubated with insect cells, Orysata, a mannose-binding lectin from rice, caused aggregation of the cells, independent from carbohydrate binding activity. This phenomenon was observed for multiple insect cell lines, confirming the robustness of this phenotype. While the carbohydrate-dependent agglutination of red blood cells happens within minutes, the carbohydrate-independent aggregation of insect cells requires longer incubation times. Further analysis with the galactose-binding lectins SSA and Jacalin, validated the robustness of this lectin-induced, carbohydrate-independent aggregation in different insect cell lines. Since proteomic analysis revealed no changes in the proteome after treatment with the lectins, this cell aggregation is likely caused by the (in) activation or re-organization of the existing surface proteins. The use of inhibitors of phosphorylation and dephosphorylation, staurosporine (STS) and a phosphatase inhibitor (PPI) cocktail, pointed to dephosphorylation as a key mechanism in the lectin-induced, carbohydrate-independent aggregation of insect cells. Similar to contact inhibition, cell proliferation in cell aggregates was decreased. Analysis of the marker for cell proliferation, cyclin E, confirmed that aggregated cells enter a quiescent state. The current data offer a new perspective on the mechanism by which lectins execute their activities, specifically through lectin-induced phosphatase-mediated cell aggregation and proliferation inhibition, independent from their carbohydrate-binding activity.

摘要

凝集素,或碳水化合物结合蛋白,可以引起特定细胞的凝集。这个过程是通过碳水化合物结合域与细胞表面糖结构的相互作用介导的,这种结合可以通过预先孵育凝集素与其特定的糖来抑制。然而,当与昆虫细胞共孵育时,来自水稻的甘露糖结合凝集素 Orysata 引起细胞的聚集,而与碳水化合物结合活性无关。这种现象在多种昆虫细胞系中都得到了观察,证实了这种表型的稳健性。虽然红细胞的碳水化合物依赖性凝集发生在几分钟内,但昆虫细胞的碳水化合物非依赖性聚集需要更长的孵育时间。用半乳糖结合凝集素 SSA 和 Jacalin 进行进一步分析,验证了这种在不同昆虫细胞系中存在的、由凝集素诱导的、碳水化合物非依赖性聚集的稳健性。由于蛋白质组学分析显示在用凝集素处理后蛋白质组没有变化,因此这种细胞聚集可能是由现有表面蛋白的(去)激活或重新组织引起的。使用磷酸化和去磷酸化抑制剂、司他丁(STS)和磷酸酶抑制剂鸡尾酒(PPI)的实验表明,去磷酸化是凝集素诱导的昆虫细胞碳水化合物非依赖性聚集的关键机制。与接触抑制类似,细胞聚集物中的细胞增殖减少。细胞增殖标志物细胞周期蛋白 E 的分析证实,聚集的细胞进入静止状态。目前的数据为凝集素执行其活性的机制提供了一个新的视角,特别是通过凝集素诱导的磷酸酶介导的细胞聚集和增殖抑制,而与它们的碳水化合物结合活性无关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验