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SCUBE1,一种新的发育基因,参与肾脏再生和修复。

SCUBE1, a novel developmental gene involved in renal regeneration and repair.

机构信息

Monash Immunology and Stem Cell Laboratories, Monash University and the Australian Stem Cell Centre, Clayton, Victoria, Australia.

出版信息

Nephrol Dial Transplant. 2010 May;25(5):1421-8. doi: 10.1093/ndt/gfp637. Epub 2009 Dec 29.

Abstract

BACKGROUND

We have identified that a novel developmental gene and protein, SCUBE1, is expressed in endothelial cells and may play an important role in kidney regeneration.

METHODS

The temporal and spatial expression of SCUBE1 was determined in a mouse model of ischaemia-reperfusion (IR) injury at 3 days and 1, 3 and 6 weeks post-injury by immunofluorescence microscopy. In vitro analysis was used to examine SCUBE1 signalling in endothelial cells under conditions of cell stress using quantitative real-time polymerase chain reaction and immunofluorescence labelling. The media from cultured endothelial cells following SCUBE1 small interfering RNA (siRNA) transfection was used to assess the proliferation capacity of epithelial cells.

RESULTS

Immunofluorescence confocal microscopy demonstrated that the SCUBE1 protein was localized to CD31-positive endothelial cells in IR kidneys during the resolution of tissue damage (3 weeks), but not in control animals. The peak expression of SCUBE1 following 3 weeks of IR injury was confirmed by reverse transcription-polymerase chain reaction. SCUBE1 mRNA and protein expression were detected in cultured endothelial cells under hypoxic conditions or serum starving. Furthermore, there was a significant decrease in epithelial cell proliferation following the addition of a supernatant derived from cultured endothelial cells following SCUBE1 siRNA gene silencing compared to control media.

CONCLUSIONS

Our results indicate that SCUBE1 may be involved in the regulation of tubular cell proliferation and re-epithelialization during the resolution of kidney injury.

摘要

背景

我们已经鉴定出一种新型发育基因和蛋白 SCUBE1,它在内皮细胞中表达,可能在肾脏再生中发挥重要作用。

方法

通过免疫荧光显微镜,在缺血再灌注(IR)损伤后 3 天和 1、3、6 周的小鼠模型中,确定 SCUBE1 的时空表达。体外分析用于使用定量实时聚合酶链反应和免疫荧光标记检查内皮细胞在细胞应激条件下的 SCUBE1 信号传导。在用 SCUBE1 小干扰 RNA(siRNA)转染培养的内皮细胞后,使用培养基来评估上皮细胞的增殖能力。

结果

免疫荧光共聚焦显微镜显示,在组织损伤(3 周)缓解期间,SCUBE1 蛋白定位于 IR 肾脏中 CD31 阳性内皮细胞,但在对照动物中则没有。通过逆转录-聚合酶链反应证实,IR 损伤后 3 周时 SCUBE1 的表达达到峰值。在缺氧条件或血清饥饿下培养的内皮细胞中检测到 SCUBE1mRNA 和蛋白表达。此外,与对照培养基相比,在用 SCUBE1 siRNA 基因沉默处理后培养的内皮细胞的上清液中,上皮细胞的增殖明显减少。

结论

我们的结果表明,SCUBE1 可能参与了肾脏损伤缓解过程中肾小管细胞增殖和再上皮化的调节。

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