Department of Medicine, University of Alabama at Birmingham, Birmingham, USA.
Nephrology Research and Training Center, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Lab Invest. 2019 Sep;99(9):1376-1388. doi: 10.1038/s41374-019-0259-0. Epub 2019 Apr 24.
Acute kidney injury (AKI) and chronic kidney disease (CKD) are interconnected syndromes with significant attributable morbidity and mortality. The disturbing trend of increasing incidence and prevalence of these clinical disorders highlights the urgent need for better understanding of the underlying mechanisms that are involved in pathogenesis of these conditions. Lymphangiogenesis and its involvement in various inflammatory conditions is increasingly recognized while its role in AKI and CKD remains to be fully elucidated. Here, we studied lymphangiogenesis in three models of kidney injury. Our results demonstrate that the main ligands for lymphangiogenesis, VEGF-C and VEGF-D, are abundantly present in tubules at baseline conditions and the expression pattern of these ligands is significantly altered following injury. In addition, we show that both of these ligands increase in serum and urine post-injury and suggest that such increment may serve as novel urinary biomarkers of AKI as well as in progression of kidney disease. We also provide evidence that irrespective of the nature of initial insult, lymphangiogenic pathways are rapidly and robustly induced as evidenced by higher expression of lymphatic markers within the kidney.
急性肾损伤 (AKI) 和慢性肾脏病 (CKD) 是相互关联的综合征,具有显著的发病和死亡率。这些临床疾病发病率和患病率不断上升的令人不安趋势突出表明,迫切需要更好地了解参与这些疾病发病机制的潜在机制。淋巴管生成及其在各种炎症疾病中的作用日益得到认可,但其在 AKI 和 CKD 中的作用仍有待充分阐明。在这里,我们在三种肾脏损伤模型中研究了淋巴管生成。我们的结果表明,淋巴管生成的主要配体 VEGF-C 和 VEGF-D 在正常情况下大量存在于肾小管中,并且这些配体的表达模式在损伤后发生显著改变。此外,我们表明,这两种配体在损伤后均增加血清和尿液中,提示这种增加可能作为 AKI 以及肾脏疾病进展的新型尿液生物标志物。我们还提供证据表明,无论初始损伤的性质如何,淋巴管生成途径都被迅速而强烈地诱导,这表现在肾脏内淋巴管生成标志物的更高表达。