与Keap1的Phenethyl Isothiocyanate (PEITC) 相互作用激活了Nrf2通路,并抑制了脂肪细胞中的脂质积累
Hae-Sun Ko1, Kwonyoung Kim2, Yu-Ran Na3
1Department of Food Science and Biotechnology, Food Clinical Research Center, Sungkyunkwan University, Suwon 16419, Korea.
The Journal of nutritional biochemistry
|May 18, 2025
概括
乙异硫酸 (PEITC) 通过激活Nrf2.2来抑制脂肪细胞的分化. 这发生在与Keap1的直接相互作用中,特别是在氨酸151中,突出了一个新的治疗标.
科学领域:
- 生物化学 生化学
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
背景情况:
- 乙异硫酸 (PEITC) 在疾病治疗方面显示出潜力.
- 脂细胞分化中的PEITC的作用及其分子通路仍然不清楚.
研究的目的:
- 为了研究PEITC对脂肪细胞分化的影响.
- 通过PEITC阐明Nrf2激活的分子机制.
主要方法:
- 评估PEITC对C3H10T1/2和3T3-L1细胞中的脂肪细胞分化的影响.
- 在Nrf2淘汰和Keap1淘汰细胞中检查了Nrf2激活.
- 使用热转移测试,共免疫沉和Keap1氨酸突变复制.
主要成果:
- 在早期脂肪生成过程中,PEITC表现出抗基效应.
- PEITC增加了Nrf2蛋白表达,取决于Keap1.1.
- PEITC直接与Keap1结合,而氨酸151对于Nrf2稳定和抗原活性至关重要.
结论:
- 通过Nrf2激活,PEITC可以抑制脂肪细胞的分化.
- 在氨酸151中,PEITC与Keap1相互作用,破坏Nrf2-Keap1复合体.
- 这项研究确定了PEITC抗脂原作用的关键机制.
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