Oh Jeong Hwan, Kim Eun-Young, Choi Youn Hee, Nam Taek-Jeong
Cell Biology Laboratory, Institute of Fisheries Sciences, Pukyong National University, Busan 46041, Republic of Korea.
Department of Marine Bio‑Materials and Aquaculture, Pukyong National University, Busan 48513, Republic of Korea.
Mol Med Rep. 2017 May;15(5):2583-2587. doi: 10.3892/mmr.2017.6285. Epub 2017 Mar 3.
Perfluorooctane sulfonate (PFOS) is a stable fluorosurfactant, which causes adverse effects in various organisms. The present study was designed to investigate the effects of Pyropia yezoensis peptide (PYP), a peptide comprised of 11 residues (ALEGGKSSGGG), on PFOS-induced endoplasmic reticulum (ER) stress in Chang cells. PFOS exposure (400 µM) for 24 h significantly decreased cell viability, which was upregulated by 250‑1,000 pg/ml PYP treatment. Exposure to PFOS also significantly increased expression of the ER stress response protein, glucose-regulated protein 78 (GRP78), and phosphorylation of extracellular signal‑regulated kinase 1/2 (ERK1/2). These elevations were significantly decreased by PYP (250 pg/ml), and, in particular, the PFOS‑induced GRP78 upregulation was decreased following treatment with 10 µM SL327, an ERK‑kinase inhibitor. However, PYP‑induced decreases in GRP78 expression and ERK1/2 phosphorylation were upregulated following treatment with LY294002 (20 µM), a phosphatidylinositol‑3 kinase (PI3K) inhibitor. PFOS-induced apoptosis was also significantly attenuated by PYP (250 pg/ml) treatment, and the PYP‑induced reduction in apoptosis was abolished by inhibition of PI3K. These findings indicate that negative regulation of ERK1/2 by PI3K is essential for the protective effects of PYP against PFOS-induced cell death, suggesting that PYP may be a candidate for therapeutic use.
全氟辛烷磺酸(PFOS)是一种稳定的含氟表面活性剂,会对多种生物产生不良影响。本研究旨在探讨由11个氨基酸残基(ALEGGKSSGGG)组成的条斑紫菜肽(PYP)对PFOS诱导的Chang细胞内质网(ER)应激的影响。暴露于400µM的PFOS 24小时显著降低细胞活力,而250 - 1000 pg/ml的PYP处理可使其上调。暴露于PFOS还显著增加了内质网应激反应蛋白葡萄糖调节蛋白78(GRP78)的表达以及细胞外信号调节激酶1/2(ERK1/2)的磷酸化。这些升高在250 pg/ml的PYP作用下显著降低,特别是在用10µM的ERK激酶抑制剂SL327处理后,PFOS诱导的GRP78上调有所降低。然而,在用磷脂酰肌醇-3激酶(PI3K)抑制剂LY294002(20µM)处理后,PYP诱导的GRP78表达降低和ERK1/2磷酸化上调。PFOS诱导的细胞凋亡也在250 pg/ml的PYP处理下显著减弱,并且抑制PI3K可消除PYP诱导的凋亡减少。这些发现表明PI3K对ERK1/2的负调节对于PYP对PFOS诱导的细胞死亡的保护作用至关重要,这表明PYP可能是一种治疗用途的候选物。