Zuk A, Gershenovich M, Ivanova Y, MacFarland R T, Fricker S P, Ledbetter S
Tissue Protection and Repair Unit, Renal Science, Genzyme R&D Center, Framingham, Massachusetts;
Pharmacology and Preclinical Development, Genzyme R&D Center, Framingham, Massachusetts; and.
Am J Physiol Renal Physiol. 2014 Oct 1;307(7):F783-97. doi: 10.1152/ajprenal.00685.2013. Epub 2014 Jul 30.
We examined whether antagonism of the CXCR₄receptor ameliorates the loss of renal function following ischemia-reperfusion. CXCR₄is ubiquitously expressed on leukocytes, known mediators of renal injury, and on bone marrow hematopoietic stem cells (HSCs). Plerixafor (AMD3100, Mozobil) is a small-molecule CXCR₄antagonist that mobilizes HSCs into the peripheral blood and also modulates the immune response in in vivo rodent models of asthma and rheumatoid arthritis. Treatment with plerixafor before and after ischemic clamping ameliorated kidney injury in a rat model of bilateral renal ischemia-reperfusion. Serum creatinine and blood urea nitrogen were significantly reduced 24 h after reperfusion, as were tissue injury and cell death. Plerixafor prevented the renal increase in the proinflammatory chemokines CXCL1 and CXCL5 and the cytokine IL-6. Flow cytometry of kidney homogenates confirmed the presence of significantly fewer leukocytes with plerixafor treatment; additionally, myeloperoxidase activity was reduced. AMD3465, a monocyclam analog of plerixafor, was similarly renoprotective. Four weeks postreperfusion, long-term effects included diminished fibrosis, inflammation, and ongoing renal injury. The mechanism by which CXCR₄inhibition ameliorates AKI is due to modulation of leukocyte infiltration and expression of proinflammatory chemokines/cytokines, rather than a HSC-mediated effect. The data suggest that CXCR₄antagonism with plerixafor may be a potential option to prevent AKI.
我们研究了CXCR₄受体拮抗剂是否能改善缺血再灌注后的肾功能丧失。CXCR₄在白细胞(已知的肾损伤介质)以及骨髓造血干细胞(HSCs)上普遍表达。普乐沙福(AMD3100,Mozobil)是一种小分子CXCR₄拮抗剂,可将造血干细胞动员到外周血中,还能在哮喘和类风湿性关节炎的体内啮齿动物模型中调节免疫反应。在双侧肾缺血再灌注大鼠模型中,在缺血夹闭前后用普乐沙福治疗可改善肾损伤。再灌注24小时后,血清肌酐和血尿素氮显著降低,组织损伤和细胞死亡也显著减少。普乐沙福可防止肾脏中促炎趋化因子CXCL1和CXCL5以及细胞因子IL-6的增加。对肾脏匀浆进行流式细胞术检测证实,普乐沙福治疗后白细胞数量显著减少;此外,髓过氧化物酶活性降低。普乐沙福的单环酰胺类似物AMD3465同样具有肾脏保护作用。再灌注四周后,长期影响包括纤维化、炎症减轻以及持续性肾损伤减少。CXCR₄抑制改善急性肾损伤的机制是通过调节白细胞浸润和促炎趋化因子/细胞因子的表达,而非造血干细胞介导的作用。数据表明,用普乐沙福拮抗CXCR₄可能是预防急性肾损伤的一个潜在选择。