INSERM U845, Centre de Recherche Croissance et Signalisation, Université Paris Descartes, Hôpital Necker Enfants Malades, Paris, France.
J Clin Invest. 2010 Nov;120(11):4065-76. doi: 10.1172/JCI42004.
Mechanisms of progression of chronic kidney disease (CKD), a major health care burden, are poorly understood. EGFR stimulates CKD progression, but the molecular networks that mediate its biological effects remain unknown. We recently showed that the severity of renal lesions after nephron reduction varied substantially among mouse strains and required activation of EGFR. Here, we utilized two mouse strains that react differently to nephron reduction--FVB/N mice, which develop severe renal lesions, and B6D2F1 mice, which are resistant to early deterioration--coupled with genome-wide expression to elucidate the molecular nature of CKD progression. Our results showed that lipocalin 2 (Lcn2, also known as neutrophil gelatinase-associated lipocalin [NGAL]), the most highly upregulated gene in the FVB/N strain, was not simply a marker of renal lesions, but an active player in disease progression. In fact, the severity of renal lesions was dramatically reduced in Lcn2-/- mice. We discovered that Lcn2 expression increased upon EGFR activation and that Lcn2 mediated its mitogenic effect during renal deterioration. EGFR inhibition prevented Lcn2 upregulation and lesion development in mice expressing a dominant negative EGFR isoform, and hypoxia-inducible factor 1α (Hif-1α) was crucially required for EGFR-induced Lcn2 overexpression. Consistent with this, cell proliferation was dramatically reduced in Lcn2-/- mice. These data are relevant to human CKD, as we found that LCN2 was increased particularly in patients who rapidly progressed to end-stage renal failure. Together our results uncover what we believe to be a novel function for Lcn2 and a critical pathway leading to progressive renal failure and cystogenesis.
慢性肾脏病(CKD)是一种主要的医疗负担,但进展机制仍不清楚。EGFR 可刺激 CKD 进展,但介导其生物学效应的分子网络仍不清楚。我们最近表明,肾单位减少后肾脏病变的严重程度在不同的小鼠品系之间有很大差异,需要激活 EGFR。在这里,我们利用两种对肾单位减少反应不同的小鼠品系——FVB/N 小鼠,其会发展出严重的肾脏病变,而 B6D2F1 小鼠则对早期恶化具有抗性——再结合全基因组表达来阐明 CKD 进展的分子本质。我们的结果表明,脂质运载蛋白 2(Lcn2,也称为中性粒细胞明胶酶相关脂质运载蛋白 [NGAL])是 FVB/N 品系中上调最明显的基因,它不仅仅是肾脏病变的标志物,而是疾病进展中的一个活跃参与者。事实上,Lcn2-/-小鼠的肾脏病变严重程度显著降低。我们发现,Lcn2 的表达在 EGFR 激活时增加,并且在肾脏恶化期间,Lcn2 介导其有丝分裂效应。在表达显性负 EGFR 同工型的小鼠中,EGFR 抑制可防止 Lcn2 上调和病变发展,并且缺氧诱导因子 1α(Hif-1α)对于 EGFR 诱导的 Lcn2 过表达至关重要。与此一致的是,Lcn2-/-小鼠的细胞增殖显著减少。这些数据与人类 CKD 相关,因为我们发现 LCN2 在那些迅速进展为终末期肾衰竭的患者中尤其增加。我们的结果揭示了 Lcn2 的一个新功能,以及一条导致进行性肾衰竭和囊形成的关键途径。