Feng Wenguang, Chen Bo, Xing Dongqi, Li Xingsheng, Fatima Huma, Jaimes Edgar A, Sanders Paul W
Divisions of Nephrology and Cardiovascular Disease, Departments of Medicine,
Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, Alabama.
J Am Soc Nephrol. 2017 Nov;28(11):3239-3250. doi: 10.1681/ASN.2017010085. Epub 2017 Jul 10.
Studies using Dahl salt-sensitive (SS) rats identified specific quantitative trait loci that predispose animals to hypertension-associated albuminuria and kidney injury. We explored the hypothesis that kidney-specific expression of the transcription factor , located within one of these loci on chromosome 8, mediates glomerular injury in SS hypertension. During the first week on a high-salt diet, SS rats and SS rats with only one functioning gene (ES rats) demonstrated similar increases in BP. However, serum creatinine concentration, albuminuria, and glomerular expression of ETS-1 and two ETS-1 targets, MCP-1 and MMP2, did not increase as substantially in ES rats as in SS rats. Mean BP subsequently increased further in SS rats and remained higher than that of ES rats for the rest of the study. After 4 weeks of high-salt intake, ES rats still showed a lower mean serum creatinine concentration and less albuminuria, as well as less histologic evidence of glomerular injury and kidney fibrosis, than SS rats did. To investigate the specific contribution of renal , we transplanted kidneys from ES or SS rats into salt-resistant SS-Chr 13 (SS-13BN) rats. Within 10 days on a high-salt diet, BP increased similarly in ES and SS allograft recipients, becoming significantly higher than the BP of control isograft recipients. However, mean serum creatinine concentration and albuminuria remained lower in ES allograft recipients than in SS allograft recipients at 2 weeks, and ES allografts showed less glomerular injury and interstitial fibrosis. In conclusion, reduced renal expression of ETS-1 prevented hypertension-associated kidney injury in SS rats.
使用 Dahl 盐敏感(SS)大鼠进行的研究确定了特定的数量性状基因座,这些基因座使动物易患高血压相关的蛋白尿和肾损伤。我们探讨了一种假说,即位于 8 号染色体上这些基因座之一内的转录因子在肾脏中的特异性表达介导了 SS 高血压中的肾小球损伤。在高盐饮食的第一周,SS 大鼠和仅具有一个功能性 基因的 SS 大鼠(ES 大鼠)的血压升高情况相似。然而,ES 大鼠的血清肌酐浓度、蛋白尿以及 ETS-1 及其两个靶点 MCP-1 和 MMP2 的肾小球表达增加幅度不如 SS 大鼠大。随后,SS 大鼠的平均血压进一步升高,并在研究的剩余时间内一直高于 ES 大鼠。高盐摄入 4 周后,与 SS 大鼠相比,ES 大鼠的平均血清肌酐浓度和蛋白尿仍较低,肾小球损伤和肾纤维化的组织学证据也较少。为了研究肾脏 的具体作用,我们将 ES 或 SS 大鼠的肾脏移植到盐抵抗的 SS-Chr 13(SS-13BN)大鼠体内。在高盐饮食 10 天内,ES 和 SS 同种异体移植受体的血压升高情况相似,且显著高于对照同基因移植受体的血压。然而,在 2 周时,ES 同种异体移植受体的平均血清肌酐浓度和蛋白尿仍低于 SS 同种异体移植受体,并且 ES 同种异体移植显示出较少的肾小球损伤和间质纤维化。总之,ETS-1 在肾脏中的表达降低可预防 SS 大鼠高血压相关的肾损伤。