Nephron. 2018;139(3):254-268. doi: 10.1159/000487492. Epub 2018 Apr 12.
Recent observational studies have shown that in chronic kidney disease (CKD) patients, a significantly smaller percentage of patients with an episode of acute kidney injury (AKI) have full recovery of renal function compared to those without CKD. However, precise mechanisms involved in the incomplete repair after AKI with preexisting CKD have not been completely ascertained. Here, we assessed the impact of preexisting CKD on the severity and recovery of AKI in a mouse model of 5/6 nephrectomy.
Male CD-1 mice underwent 5/6 nephrectomy (Nx). Six weeks post surgery, ischemia reperfusion injury (IRI) or a sham operation was performed and functional, histological, and various molecular parameters were compared between them.
Serum creatinine level on day 1 after IRI was comparable between control and Nx mice. However, serum creatinine remained significantly higher throughout the recovery phase in Nx mice compared to control mice. mRNA and protein expression of the cell cycle regulatory proteins were persistently elevated in Nx mice and this was associated with significantly increased levels of the G1 cell cycle arrest markers. Treatment with a p53 inhibitor following IRI resulted in not only decreased expression of G1 arrest markers but also decreased fibrosis, suggesting that prolonged epithelial G1 cell cycle arrest might be partially responsible for impaired recovery from superimposed AKI on CKD.
Taken together, reduced nephron mass have a negative effect on the repair process that is partially mediated by the disruption of the cell cycle regulation.
最近的观察性研究表明,在慢性肾脏病(CKD)患者中,与无 CKD 的患者相比,发生急性肾损伤(AKI)的患者中肾功能完全恢复的比例明显较小。然而,与 CKD 并存的 AKI 后不完全修复的确切机制尚未完全确定。在这里,我们在 5/6 肾切除术的小鼠模型中评估了预先存在的 CKD 对 AKI 的严重程度和恢复的影响。
雄性 CD-1 小鼠接受 5/6 肾切除术(Nx)。手术后 6 周,进行缺血再灌注损伤(IRI)或假手术,并比较它们之间的功能、组织学和各种分子参数。
IRI 后第 1 天血清肌酐水平在对照组和 Nx 小鼠之间无差异。然而,与对照组相比,Nx 小鼠在整个恢复期的血清肌酐水平仍明显升高。Nx 小鼠的细胞周期调控蛋白的 mRNA 和蛋白表达持续升高,这与 G1 细胞周期阻滞标志物的水平显著升高相关。IRI 后用 p53 抑制剂治疗不仅降低了 G1 阻滞标志物的表达,还降低了纤维化,这表明上皮细胞 G1 细胞周期阻滞的延长可能部分导致 CKD 叠加 AKI 后的恢复受损。
总之,肾单位质量的减少对修复过程有负面影响,部分是由细胞周期调控的破坏介导的。