在条件培养基中dj -1敲除细胞和dj -1敲除小鼠血清中豆素分泌增加。

The Open Biochemistry Journal Pub Date : 2018-02-28 eCollection Date: 2018-01-01 DOI:10.2174/1874091X01812010029
Takuya Yamane, Izumi Kato-Ose, Tatsuji Sakamoto, Yoshihisa Nakano
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引用次数: 0

摘要

背景:天冬酰胺内肽酶,也被称为豆素(EC 3.4.22.34)在小鼠肾脏中显示出很强的活性。Legumain在肿瘤中也高度表达。DJ-1/PARK7是一种帕金森病和癌症相关蛋白。DJ-1是多种转录因子的辅激活因子。最近,我们报道了p53通过DJ-1调控豆科蛋白基因的转录。方法:采用Western blotting和ELISA检测DJ-1敲除细胞条件培养基和DJ-1敲除小鼠血清中豆科蛋白的分泌水平。我们对豆科蛋白进行免疫细胞化学染色,以检测豆科蛋白在dj -1敲除细胞中的定位。结果:我们发现dj -1敲除细胞的条件培养基和dj -1敲除小鼠的血清中豆素的分泌水平升高。在dj -1敲除细胞中,豆科蛋白的斑点结构也增加。结论:dj -1敲除细胞和小鼠的豆科蛋白分泌增加是通过增加其在膜相关囊泡中的表达和积累来实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Secretion of Legumain Increases in Conditioned Medium from DJ-1-Knockout Cells and in Serum from DJ-1-Knockout Mice.

Secretion of Legumain Increases in Conditioned Medium from DJ-1-Knockout Cells and in Serum from DJ-1-Knockout Mice.

Secretion of Legumain Increases in Conditioned Medium from DJ-1-Knockout Cells and in Serum from DJ-1-Knockout Mice.

Secretion of Legumain Increases in Conditioned Medium from DJ-1-Knockout Cells and in Serum from DJ-1-Knockout Mice.

Background: Asparaginyl endopeptidase, also known as legumain (EC 3.4.22.34) shows strong activity in the mouse kidney. Legumain is also highly expressed in tumors. DJ-1/PARK7 is a Parkinson's disease- and cancer-associated protein. DJ-1 is a coactivator of various transcription factors. Recently, we reported that transcription of the legumain gene is regulated by p53 through DJ-1.

Methods: We measured the secretion levels of legumain in a conditioned medium of DJ-1 knockout cells and in serum from DJ-1 knockout mice using Western blotting and ELISA. We performed immunocytochemical staining of legumain to examine the localization of legumain in DJ-1-knockout cells.

Results: We found that the secretion levels of legumain were increased in the conditioned medium of DJ-1-knockout cells and in serum from DJ-1-knockout mice. Dot structures of legumain were also increased in DJ-1-knockout cells.

Conclusion: The results suggest that legumain secretion from DJ-1-knockout cells and in mice increases through its increased expression and accumulation in membrane-associated vesicles.

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