Lee Jin-Yong, Tokumoto Maki, Fujiwara Yasuyuki, Satoh Masahiko
Laboratory of Pharmaceutical Health Sciences, School of Pharmacy, Aichi Gakuin University.
J Toxicol Sci. 2015 Dec;40(6):901-8. doi: 10.2131/jts.40.901.
Cadmium (Cd) is a toxic heavy metal with a long half-life in humans. It causes disorders of various tissue systems, including the kidney, and is associated with protein aggregation. Our previous study demonstrated Cd-induced suppression of the UBE2D gene family, one of the ubiquitin-conjugating enzyme families. However, the precise role of ubiquitin-coding genes in Cd toxicity remains to be understood. In this study, we investigated the effect of Cd on expression of the ubiquitin-coding genes UBB, UBC, UBA80, and UBA52 in HK-2 human proximal tubular cells. Prior to the appearance of Cd toxicity, the UBB, UBC, and UBA80 expression levels increased following Cd treatment. Knockdown of UBB by siRNA transfection significantly decreased Cd cytotoxicity. Notably, Cd induces ubiquitinated protein levels in HK-2 cells, and knockdown of UBB blocked this process. These results suggest that UBB is involved in Cd-induced increase of protein ubiquitination, and that accumulation of ubiquitinated proteins through increased UBB expression may contribute to Cd toxicity in HK-2 cells.
镉(Cd)是一种对人体具有较长半衰期的有毒重金属。它会导致包括肾脏在内的各种组织系统紊乱,并与蛋白质聚集有关。我们之前的研究表明,镉会抑制泛素结合酶家族之一的UBE2D基因家族。然而,泛素编码基因在镉毒性中的精确作用仍有待了解。在本研究中,我们调查了镉对HK-2人近端肾小管细胞中泛素编码基因UBB、UBC、UBA80和UBA52表达的影响。在镉毒性出现之前,镉处理后UBB、UBC和UBA80的表达水平升高。通过siRNA转染敲低UBB可显著降低镉的细胞毒性。值得注意的是,镉会诱导HK-2细胞中泛素化蛋白水平升高,而敲低UBB可阻断这一过程。这些结果表明,UBB参与了镉诱导的蛋白质泛素化增加,并且通过增加UBB表达导致的泛素化蛋白积累可能有助于HK-2细胞中的镉毒性。