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羟脯氨酸减轻4-羟基-2-壬烯醛诱导的猪肠上皮细胞DNA损伤和凋亡。

Hydroxyproline alleviates 4-hydroxy-2-nonenal-induced DNA damage and apoptosis in porcine intestinal epithelial cells.

作者信息

Ji Yun, He Yu, Yang Ying, Dai Zhaolai, Wu Zhenlong

机构信息

State Key Laboratory of Animal Nutrition, Department of Animal Nutrition and Feed Science, China Agricultural University, Beijing 100193, China.

Beijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, Beijing 100193, China.

出版信息

Anim Nutr. 2021 Oct 16;9:7-15. doi: 10.1016/j.aninu.2021.08.003. eCollection 2022 Jun.

Abstract

Oxidative stress has been confirmed in relation to intestinal mucosa damage and multiple bowel diseases. Hydroxyproline (Hyp) is an imino acid abundant in sow's milk. Compelling evidence has been gathered showing the potential antioxidative properties of Hyp. However, the role and mechanism of Hyp in porcine intestinal epithelial cells in response to oxidative stress remains unknown. In this study, small intestinal epithelial cell lines of piglets (IPEC-1) were used to evaluate the protective effects of Hyp on 4-hydroxy-2-nonenal (4-HNE)-induced oxidative DNA damage and apoptosis. IPEC-1 pretreated with 0.5 to 5 mmol/L Hyp were exposed to 4-HNE (40 μmol/L) in the presence or absence of Hyp. Thereafter, the cells were subjected to apoptosis detection by Hoechst staining, flow cytometry, and Western blot or DNA damage analysis by comet assay, immunofluorescence, and reverse-transcription quantitative PCR (RT-qPCR). Cell apoptosis and the upregulation of cleaved-caspase-3 induced by 4-HNE (40 μmol/L) were inhibited by 5 mmol/L of Hyp. In addition, 5 mmol/L Hyp attenuated 4-HNE-induced reactive oxygen species (ROS) accumulation, glutathione (GSH) deprivation and DNA damage. The elevation in transcription of (growth arrest and DNA-damage-inducible protein 45 alpha) and (growth arrest and DNA-damage-inducible protein 45 beta), as well as the phosphorylation of H2AX (H2A histone family, member X), p38 MAPK (mitogen-activated protein kinase), and JNK (c-Jun N-terminal kinase) in cells treated with 4-HNE were alleviated by 5 mmol/L Hyp. Furthermore, Hyp supplementation increased the protein abundance of Krüppel like factor 4 (KLF4) in cells exposed to 4-HNE. Suppression of KLF4 expression by kenpaulone impeded the resistance of Hyp-treated cells to DNA damage and apoptosis induced by 4-HNE. Collectively, our results indicated that Hyp serves to protect against 4-HNE-induced apoptosis and DNA damage in IPEC-1 cells, which is partially pertinent with the enhanced expression of KLF4. Our data provides an updated explanation for the nutritional values of Hyp-containing animal products.

摘要

氧化应激与肠黏膜损伤及多种肠道疾病有关已得到证实。羟脯氨酸(Hyp)是母乳中丰富的一种亚氨基酸。已有确凿证据表明Hyp具有潜在的抗氧化特性。然而,Hyp在猪肠道上皮细胞中应对氧化应激的作用和机制仍不清楚。在本研究中,使用仔猪小肠上皮细胞系(IPEC-1)来评估Hyp对4-羟基-2-壬烯醛(4-HNE)诱导的氧化性DNA损伤和细胞凋亡的保护作用。用0.5至5 mmol/L Hyp预处理的IPEC-1在有或无Hyp存在的情况下暴露于4-HNE(40 μmol/L)。此后,通过Hoechst染色、流式细胞术和蛋白质印迹法进行细胞凋亡检测,或通过彗星试验、免疫荧光和逆转录定量PCR(RT-qPCR)进行DNA损伤分析。5 mmol/L的Hyp可抑制4-HNE(40 μmol/L)诱导的细胞凋亡以及裂解的半胱天冬酶-3的上调。此外,5 mmol/L Hyp可减轻4-HNE诱导的活性氧(ROS)积累、谷胱甘肽(GSH)耗竭和DNA损伤。5 mmol/L Hyp可减轻4-HNE处理的细胞中(生长停滞和DNA损伤诱导蛋白45α)和(生长停滞和DNA损伤诱导蛋白45β)转录的升高,以及H2AX(H2A组蛋白家族成员X)、p38丝裂原活化蛋白激酶(MAPK)和c-Jun氨基末端激酶(JNK)的磷酸化。此外,补充Hyp可增加暴露于4-HNE的细胞中Krüppel样因子4(KLF4)的蛋白丰度。肯帕罗酮抑制KLF4表达会阻碍Hyp处理的细胞对4-HNE诱导的DNA损伤和细胞凋亡的抗性。总体而言,我们的结果表明Hyp可保护IPEC-1细胞免受4-HNE诱导的细胞凋亡和DNA损伤,这部分与KLF4表达增强有关。我们的数据为含Hyp的动物产品的营养价值提供了新的解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c582/9344311/1a542d91e508/gr1.jpg

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