首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >The effects of adenosine A2A receptor knockout on renal interstitial fibrosis in a mouse model of unilateral ureteral obstruction
【24h】

The effects of adenosine A2A receptor knockout on renal interstitial fibrosis in a mouse model of unilateral ureteral obstruction

机译:腺苷A2A受体敲除对单侧输尿管梗阻小鼠模型中肾间质纤维化的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Adenosine A2A receptor (A2AR) plays an important regulatory role in the processes of inflammation and fibrosis. However, it is unknown whether A2AR can mediate renal interstitial fibrosis (RIF). To evaluate the effect of genetic A2AR knockout (KO) on the pathological progress of RIF, we applied a unilateral ureteral obstruction (UUO) model of RIF on A2AR KO mice and their wild-type (WT) littermates. Renal pathological assessment was performed at different post-UUO stages using hematoxylin and eosin (H&E) and Masson's trichrome staining as well as quantitative morphological analysis. Our data demonstrated that: (i) the extent of RIF was determined by the development of UUO in a time-dependent manner; (ii) A2AR KO exacerbated the pathological progress of RIF in mice at the early post-UUO stage, i.e. day 3 and day 7; (iii) the profibrotic effect of A2AR KO was prominent until the late post-UUO stage, i.e. day 14, at which RIF reached a similar severity level in A2AR KO and WT mice. Our findings revealed that A2AR KO significantly exacerbated the progression of UUO-induced RIF in mice, prominently at the initial stage.
机译:腺苷A2A受体(A2AR)在炎症和纤维化过程中起重要的调节作用。但是,尚不清楚A2AR是否可以介导肾间质纤维化(RIF)。为了评估基因A2AR基因敲除(KO)对RIF病理进展的影响,我们将RIF的单侧输尿管阻塞(UUO)模型应用于A2AR KO小鼠及其野生型(WT)同窝仔。使用苏木精和曙红(H&E)和Masson三色染色以及定量形态学分析,在UUO后不同阶段进行肾脏病理评估。我们的数据表明:(i)RIF的程度由UUO的发展以时间依赖的方式决定; (ii)在UUO后早期,即第3天和第7天,A2AR KO加剧了RIF在小鼠中的病理学进展; (iii)直到UUO后后期,即第14天,RIF在A2AR KO和WT小鼠中达到相似的严重性水平之前,A2AR KO的纤维化作用才是显着的。我们的发现表明,A2AR KO在初始阶段显着加重了UUO诱导的RIF在小鼠中的进程。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号