Suppr超能文献

新型动物模型中刀豆球蛋白 A 诱导肝细胞凋亡的研究:可能涉及非 caspase 依赖性途径。

New Insight into the Concanavalin A-Induced Apoptosis in Hepatocyte of an Animal Model: Possible Involvement of Caspase-Independent Pathway.

机构信息

Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

Key Laboratory of Organ Transplantation, Ministry of Education, NHC Key Laboratory of Organ Transplantation, Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Wuhan 430030, China.

出版信息

Molecules. 2023 Jan 30;28(3):1312. doi: 10.3390/molecules28031312.

Abstract

Concanavalin A (Con A) is known to be a T-cell mitogen and has been shown to induce hepatitis in mice through the triggering of conventional T cells and NKT cells. However, it remains unknown whether Con A itself can directly induce rapid hepatocyte death in the absence of a functional immune system. Here, by using an immunodeficient mouse model, we found Con A rapidly induced liver injury in vivo despite a lack of immunocyte involvement. We further observed in vitro that hepatocytes underwent a dose-dependent but caspase-independent apoptosis in response to Con A stimulation in vitro. Moreover, transcriptome RNA-sequencing analysis revealed that apoptosis pathways were activated in both our in vivo and in vitro models. We conclude that Con A can directly induce rapid but non-classical apoptosis in hepatocytes without the participation of immunocytes. These findings provide new insights into the mechanism of Con A-induced hepatitis.

摘要

刀豆球蛋白 A(Con A)已知是一种 T 细胞有丝分裂原,并已被证明通过触发常规 T 细胞和 NKT 细胞在小鼠中引发肝炎。然而,目前尚不清楚 Con A 本身是否可以在没有功能性免疫系统的情况下直接诱导肝细胞快速死亡。在这里,我们通过使用免疫缺陷小鼠模型发现,尽管没有免疫细胞参与,Con A 仍能在体内迅速诱导肝损伤。我们进一步在体外观察到,肝细胞在体外受到 Con A 刺激后,发生剂量依赖性但半胱天冬酶非依赖性凋亡。此外,转录组 RNA 测序分析表明,凋亡途径在我们的体内和体外模型中均被激活。我们得出结论,Con A 可以直接诱导肝细胞发生快速但非经典的凋亡,而无需免疫细胞的参与。这些发现为 Con A 诱导肝炎的机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8501/9919242/a73d2a283ed7/molecules-28-01312-g001.jpg

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