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TRPM2 激活可能参与了 5-氟尿嘧啶诱导的小鼠骨髓抑制。

Possible involvement of TRPM2 activation in 5-fluorouracil-induced myelosuppression in mice.

机构信息

Division of Physiology and Pathology, Faculty of Pharmaceutical Sciences, Teikyo Heisei University, Nakano, Tokyo, 164-8530, Japan; Division of Physiology and Pathology, Department of Pharmacology, Toxicology and Therapeutics, Showa University School of Pharmacy, Shinagawa, Tokyo, 142-8555, Japan.

Division of Pharmacology, Faculty of Pharmaceutical Sciences, Teikyo Heisei University, Nakano, Tokyo, 164-8530, Japan.

出版信息

Eur J Pharmacol. 2021 Jan 15;891:173671. doi: 10.1016/j.ejphar.2020.173671. Epub 2020 Oct 22.

Abstract

Transient receptor potential melastatin 2 (TRPM2) is an oxidative stress-sensitive Ca-permeable channel. The activation of TRPM2 by HO causes cell death in various types of cells. 5-Fluorouracil (5-FU) is an important anticancer drug, but myelosuppression is one of the most frequent adverse effects. The involvement of oxidative stress in 5-FU-induced myelosuppression has been reported, and bone marrow cells are known to express TRPM2. The aim of this study was to investigate whether TRPM2 is involved in 5-FU-induced myelosuppression. Enhancement of HO-induced intracellular Ca concentration ([Ca]) increase by 5-FU treatment was observed in human embryonic kidney 293 (HEK) cells stably expressing TRPM2 but not in HEK cells, indicating that 5-FU stimulates TRPM2 activation. In CD117 positive cells from wild type (WT) mouse bone marrow, 5-FU also enhanced the HO-induced [Ca] increases, but not in cells from Trpm2 knockout (KO) mice. In the CFU-GM colony assay, the 5-FU-induced reduction of colony number was alleviated by Trpm2 deficiency. Moreover, the reduction of leukocytes in blood by administration with 5-FU in WT mice was also alleviated in Trpm2 KO mice. The activation of TRPM2 in bone marrow cells seems to be involved in 5-FU-induced myelosuppression.

摘要

瞬时受体电位 melastatin 2(TRPM2)是一种氧化应激敏感的 Ca 通透性通道。HO 激活 TRPM2 可导致多种类型细胞死亡。5-氟尿嘧啶(5-FU)是一种重要的抗癌药物,但骨髓抑制是最常见的不良反应之一。氧化应激参与 5-FU 诱导的骨髓抑制已有报道,且骨髓细胞表达 TRPM2。本研究旨在探讨 TRPM2 是否参与 5-FU 诱导的骨髓抑制。在稳定表达 TRPM2 的人胚肾 293(HEK)细胞中,5-FU 增强了 HO 诱导的细胞内 Ca 浓度([Ca])增加,而在 HEK 细胞中则没有,表明 5-FU 刺激 TRPM2 激活。在 WT 小鼠骨髓中 CD117 阳性细胞中,5-FU 也增强了 HO 诱导的 [Ca]增加,但在 Trpm2 敲除(KO)小鼠的细胞中则没有。在 CFU-GM 集落形成实验中,TRPM2 缺失减轻了 5-FU 诱导的集落数减少。此外,WT 小鼠给予 5-FU 后血液中白细胞减少也在 Trpm2 KO 小鼠中得到缓解。骨髓细胞中 TRPM2 的激活似乎参与了 5-FU 诱导的骨髓抑制。

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