| Literature DB >> 27080942 |
Dan Wang1,2, Xiao-Wei Li1,2, Xuan Wang2, Huan-Ran Tan3, Yan Jia4, Li Yang4, Xiao-Mei Li4, Ming-Ying Shang1, Feng Xu1, Xing-Xin Yang1, Yukihiro Shoyama5, Shao-Qing Cai1.
Abstract
Aristolochic acid I (AA-I) is a strong nephrotoxin, carcinogen, and mutagen found in plants such as the Aristolochia species. The mechanisms underlying AA-I toxicity in the kidneys are poorly understood. In this study, we aimed to gain insight into the mechanism of AA-I nephrotoxicity by analyzing the uptake, subcellular distribution, and intracellular targets of AA-I in the human kidney cell line HK-2 using immunocytochemistry, immunoprecipitation, and LC-MS/MS. In HK-2 cells incubated with 20[Formula: see text][Formula: see text]g/mL AA-I for different periods of time (up to 12[Formula: see text]h), AA-I was detected by a specific monoclonal antibody (MAb) against AA-I, both in the cytoplasm and nuclei. Nuclear localization depended on the exposure time. A protein with the molecular weight of 100 kDa was immunoprecipitated with the anti-AA-I MAb from the AA-I-treated cell lysates and was identified by LC-MS/MS as [Formula: see text]-actinin-4 after digestion of the protein, and was confirmed by immunoblotting with a specific anti-[Formula: see text]-actinin-4 MAb. This evidence shows, for the first time, that [Formula: see text]-actinin-4 is a protein targeted by AA-I in kidney cells. Our findings strongly suggest an association between [Formula: see text]-actinin-4 and AA-I nephrotoxic activity.Entities:
Keywords: -Actinin-4; Aristolochic Acid; HK-2 Cells; IP-MS/MS; Immunocytochemistry; Immunoprecipitation (IP); Monoclonal Antibody
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Year: 2016 PMID: 27080942 DOI: 10.1142/S0192415X16500178
Source DB: PubMed Journal: Am J Chin Med ISSN: 0192-415X Impact factor: 4.667