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对氧磷酶可保护视网膜色素上皮细胞免受毒死蜱的损害。

Paraoxonase enzyme protects retinal pigment epithelium from chlorpyrifos insult.

作者信息

Jasna Jagan Mohan, Anandbabu Kannadasan, Bharathi Subramaniam Rajesh, Angayarkanni Narayanasamy

机构信息

R.S Mehta Jain Department of Biochemistry and Cell Biology, KBIRVO Block, Vision Research Foundation, Sankara Nethralaya, Chennai, India.

出版信息

PLoS One. 2014 Jun 30;9(6):e101380. doi: 10.1371/journal.pone.0101380. eCollection 2014.

DOI:10.1371/journal.pone.0101380
PMID:24979751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4076322/
Abstract

Retinal pigment epithelium (RPE) provides nourishment and protection to the eye. RPE dysfunction due to oxidative stress and inflammation is one of the major reason for many of the retinal disorders. Organophosphorus pesticides are widely used in the agricultural, industrial and household activities in India. However, their effects on the eye in the context of RPE has not been studied. In this study the defense of the ARPE19 cells exposed to Chlorpyrifos (1 nM to 100 µM) in terms of the enzyme paraoxonase (PON) was studied at 24 hr and 9 days of treatment. Chlorpyrifos was found to induce oxidative stress in the ARPE19 cells as seen by significant increase in ROS and decrease in glutathione (GSH) levels without causing cell death. Tissue resident Paraoxonase 2 (PON2) mRNA expression was elevated with chlorpyrifos exposure. The three enzymatic activities of PON namely, paraoxonase (PONase), arylesterase (PON AREase) and thiolactonase (PON HCTLase) were also found to be significantly altered to detoxify and as an antioxidant defense. Among the transcription factors regulating PON2 expression, SP1 was significantly increased with chlorpyrifos exposure. PON2 expression was found to be crucial as ARPE19 cells showed a significant loss in their ability to withstand oxidative stress when the cells were subjected to chlorpyrifos after silencing PON2 expression. Treatment with N-acetyl cysteine positively regulated the PON 2 expression, thus promoting the antioxidant defense put up by the cells in response to chlorpyrifos.

摘要

视网膜色素上皮(RPE)为眼睛提供营养和保护。由于氧化应激和炎症导致的RPE功能障碍是许多视网膜疾病的主要原因之一。有机磷农药在印度的农业、工业和家庭活动中广泛使用。然而,它们在RPE背景下对眼睛的影响尚未得到研究。在本研究中,在处理24小时和9天时,研究了暴露于毒死蜱(1 nM至100 μM)的ARPE19细胞在对氧磷酶(PON)方面的防御作用。发现毒死蜱可诱导ARPE19细胞中的氧化应激,表现为活性氧显著增加和谷胱甘肽(GSH)水平降低,但未导致细胞死亡。随着毒死蜱暴露,组织驻留对氧磷酶2(PON2)mRNA表达升高。还发现PON的三种酶活性,即对氧磷酶(PONase)、芳基酯酶(PON AREase)和硫内酯酶(PON HCTLase)发生了显著改变,以进行解毒并作为抗氧化防御。在调节PON2表达的转录因子中,随着毒死蜱暴露,SP1显著增加。发现PON2表达至关重要,因为当沉默PON2表达后使细胞暴露于毒死蜱时,ARPE19细胞承受氧化应激的能力显著丧失。用N-乙酰半胱氨酸处理可正向调节PON 2表达,从而促进细胞对毒死蜱作出反应时的抗氧化防御。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/2efb7af6d17a/pone.0101380.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/d8ad644c5ae0/pone.0101380.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/97363abe9c17/pone.0101380.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/6976294bb84a/pone.0101380.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/b5eaae1f2928/pone.0101380.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/2efb7af6d17a/pone.0101380.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/d8ad644c5ae0/pone.0101380.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/97363abe9c17/pone.0101380.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/6976294bb84a/pone.0101380.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/b5eaae1f2928/pone.0101380.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4009/4076322/2efb7af6d17a/pone.0101380.g005.jpg

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