Fujiki K, Inamura H, Matsuoka M
Department of Hygiene and Public Health I, Tokyo Women's Medical University, Tokyo, Japan.
Cell Death Dis. 2014 Aug 14;5(8):e1378. doi: 10.1038/cddis.2014.339.
We examined the roles of Notch1 signaling and its cross-talk with other signaling pathways, including p53 and phosphatidylinositol-3-kinase (PI3K)/Akt, in cadmium-induced cellular damage in HK-2 human renal proximal tubular epithelial cells. Following exposure to cadmium chloride (CdCl2), the level of Notch intracellular domain (NICD), the cleaved form of the Notch1 receptor, was increased and accumulated in the nuclear fraction. Knockdown of Notch1 with siRNA or treatment with the γ-secretase inhibitor, DAPT (N-[N-(3,5-difluorophenacetyl-L-alanyl)]-S-phenylglycine t-butyl ester), prevented CdCl2-induced morphological change of HK-2 cells and reduction of cell viability. Knockdown of Jagged1 or Jagged2, the ligands of the Notch1 receptor, partially suppressed cadmium cytotoxicity. Inhibition of p53 activity with pifithrin-α or inhibition of PI3K with LY294002 suppressed CdCl2-induced cellular damage and elevation of Notch1-NICD. In addition, treatment with the epidermal growth factor receptor (EGFR) inhibitor, AG1478, and the insulin-like growth factor-1 receptor inhibitor, PPP, suppressed both Notch1-NICD accumulation and Akt phosphorylation in HK-2 cells exposed to CdCl2. However, knockdown of Notch1 did not affect CdCl2-induced p53 accumulation and phosphorylation but suppressed phosphorylation of EGFR, Akt, and p70 S6 kinase. Depletion of Notch1 suppressed CdCl2-induced reduction of E-cadherin expression and elevation of Snail expression. Furthermore, treatment with SB216763, an inhibitor of glycogen synthase kinase-3, suppressed the potency of LY294002 treatment to reduce Snail expression in HK-2 cells exposed to CdCl2. Knockdown of Snail with siRNA partially prevented HK-2 cells from CdCl2-induced reduction of E-cadherin expression and cellular damage. These results suggest that cadmium exposure induces the activation of Notch1 signaling in renal proximal tubular cells with cooperative activation by the p53 and PI3K/Akt signaling pathways; the resultant expression of Snail, a repressor of E-cadherin expression, might lead to cellular damage by decreasing cell-cell adhesion.
我们研究了Notch1信号通路及其与其他信号通路(包括p53和磷脂酰肌醇-3-激酶(PI3K)/Akt)的相互作用在氯化镉诱导的HK-2人肾近端小管上皮细胞损伤中的作用。暴露于氯化镉(CdCl2)后,Notch细胞内结构域(NICD)(Notch1受体的裂解形式)的水平升高并在核部分中积累。用小干扰RNA(siRNA)敲低Notch1或用γ-分泌酶抑制剂DAPT(N-[N-(3,5-二氟苯乙酰基-L-丙氨酰基)]-S-苯基甘氨酸叔丁酯)处理可防止CdCl2诱导的HK-2细胞形态变化和细胞活力降低。敲低Notch1受体的配体Jagged1或Jagged2可部分抑制镉的细胞毒性。用pifithrin-α抑制p53活性或用LY294002抑制PI3K可抑制CdCl2诱导的细胞损伤和Notch1-NICD升高。此外,用表皮生长因子受体(EGFR)抑制剂AG1478和胰岛素样生长因子-1受体抑制剂PPP处理可抑制暴露于CdCl2的HK-2细胞中Notch1-NICD的积累和Akt磷酸化。然而,敲低Notch1并不影响CdCl2诱导的p53积累和磷酸化,但可抑制EGFR、Akt和p70 S6激酶的磷酸化。Notch1的缺失抑制了CdCl2诱导的E-钙黏蛋白表达降低和Snail表达升高。此外,用糖原合酶激酶-3抑制剂SB216763处理可抑制LY294002处理在暴露于CdCl2的HK-2细胞中降低Snail表达的效力。用siRNA敲低Snail可部分防止HK-2细胞中CdCl2诱导的E-钙黏蛋白表达降低和细胞损伤。这些结果表明,镉暴露通过p53和PI3K/Akt信号通路的协同激活诱导肾近端小管细胞中Notch1信号通路的激活;E-钙黏蛋白表达抑制因子Snail的表达升高可能通过降低细胞间黏附导致细胞损伤。