泛素编码基因参与镉诱导的人近端小管细胞蛋白泛素化。

Jin-Yong Lee, M. Tokumoto, Y. Fujiwara, M. Satoh
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引用次数: 16

摘要

镉(Cd)是一种有毒的重金属,在人体内的半衰期很长。它引起各种组织系统的紊乱,包括肾脏,并与蛋白质聚集有关。我们之前的研究证实了cd诱导UBE2D基因家族的抑制,UBE2D基因家族是泛素结合酶家族之一。然而,泛素编码基因在镉毒性中的确切作用尚不清楚。在本研究中,我们研究了Cd对HK-2人近端小管细胞中泛素编码基因UBB、UBC、UBA80和UBA52表达的影响。在出现Cd毒性之前,UBB、UBC和UBA80的表达水平在Cd治疗后增加。转染siRNA敲低UBB可显著降低Cd细胞毒性。值得注意的是,Cd诱导HK-2细胞中的泛素化蛋白水平,而UBB的敲低阻断了这一过程。这些结果表明,UBB参与了Cd诱导的蛋白泛素化的增加,泛素化蛋白通过UBB表达的增加而积累可能有助于Cd对HK-2细胞的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Involvement of ubiquitin-coding genes in cadmium-induced protein ubiquitination in human proximal tubular cells.
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.
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