[Notch1和ALK4/5信号通路参与肾小管细胞死亡:它们在澄清镉毒性中的应用]。

Q3 Medicine
Kota Fujiki
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引用次数: 0

摘要

肾小管细胞死亡是由各种细胞外应激引起的,包括中毒量的镉(一种职业和环境污染金属),并导致肾功能障碍。虽然镉暴露破坏了许多细胞内信号通路,但镉诱导肾小管细胞死亡的分子机制尚未完全阐明。我们最近发现了促进镉诱导肾小管细胞死亡的两个重要细胞内信号通路:Notch1信号通路和激活素受体样激酶(ALK) 4/5信号通路(也称为激活素转化生长因子β受体途径)。在这篇综述文章中,我们介绍了我们之前的实验发现,重点是Notch1和ALK4/5信号通路,这些信号通路可能揭示镉诱导肾小管细胞死亡的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Involvement of Notch1 and ALK4/5 Signaling Pathways in Renal Tubular Cell Death: Their Application to Clarification of Cadmium Toxicity].

Renal tubular cell death is caused by various extracellular stresses including toxic amounts of cadmium, an occupational and environmental pollutant metal, and is responsible for renal dysfunction. While cadmium exposure disrupts many intracellular signaling pathways, the molecular mechanism underlying cadmium-induced renal tubular cell death has not yet been fully elucidated. We have recently identified two important intracellular signaling pathways that promote cadmium-induced renal tubular cell death: the Notch1 signaling and activin receptor-like kinase (ALK) 4/5 signaling (also known as the activin-transforming growth factor β receptor pathways). In this review paper, we introduce our previous experimental findings, focusing on Notch1 and ALK4/5 signaling pathways, which may uncover the molecular mechanisms involved in cadmium-induced renal tubular cell death.

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来源期刊
Japanese Journal of Hygiene
Japanese Journal of Hygiene Medicine-Medicine (all)
CiteScore
0.90
自引率
0.00%
发文量
7
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