Walter Brendel Centre of Experimental Medicine, Biomedical Center, Institute of Cardiovascular Physiology and Pathophysiology, Ludwig-Maximilians-University Munich, Planegg-Martinsried, Germany.
Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians University, Munich, Germany.
Front Immunol. 2020 Dec 22;11:588245. doi: 10.3389/fimmu.2020.588245. eCollection 2020.
Uromodulin (UMOD) is produced and secreted by tubular epithelial cells. Secreted UMOD polymerizes (pUMOD) in the tubular lumen, where it regulates salt transport and protects the kidney from bacteria and stone formation. Under various pathological conditions, pUMOD accumulates within the tubular lumen and reaches extratubular sites where it may interact with renal interstitial cells. Here, we investigated the potential of extratubular pUMOD to act as a damage associated molecular pattern (DAMP) molecule thereby creating local inflammation. We found that intrascrotal and intraperitoneal injection of pUMOD induced leukocyte recruitment and led to TNF-α secretion by F4/80 positive macrophages. Additionally, pUMOD directly affected vascular permeability and increased neutrophil extravasation independent of macrophage-released TNF-α. Interestingly, pUMOD displayed no chemotactic properties on neutrophils, did not directly activate β2 integrins and did not upregulate adhesion molecules on endothelial cells. In obstructed neonatal murine kidneys, we observed extratubular UMOD accumulation in the renal interstitium with tubular atrophy and leukocyte infiltrates. Finally, we found extratubular UMOD deposits associated with peritubular leukocyte infiltration in kidneys from patients with inflammatory kidney diseases. Taken together, we identified extratubular pUMOD as a strong inducer of leukocyte recruitment, underlining its critical role in mounting an inflammatory response in various kidneys pathologies.
尿调蛋白(UMOD)由管状上皮细胞产生和分泌。分泌的 UMOD 在管状腔中聚合(pUMOD),在那里它调节盐的运输,并保护肾脏免受细菌和结石形成的影响。在各种病理条件下,pUMOD 在管状腔内积聚,并到达肾小管外部位,在那里它可能与肾间质细胞相互作用。在这里,我们研究了肾小管外 pUMOD 作为损伤相关分子模式(DAMP)分子的潜力,从而引发局部炎症。我们发现,pUMOD 的鞘内和腹腔内注射诱导了白细胞募集,并导致 F4/80 阳性巨噬细胞分泌 TNF-α。此外,pUMOD 直接影响血管通透性,并增加中性粒细胞渗出,而不依赖于巨噬细胞释放的 TNF-α。有趣的是,pUMOD 对中性粒细胞没有趋化作用,不直接激活β2 整合素,也不在上皮细胞上上调黏附分子。在梗阻性新生鼠肾脏中,我们观察到肾小管外 UMOD 在肾间质中的积聚,伴有肾小管萎缩和白细胞浸润。最后,我们发现炎症性肾脏疾病患者的肾脏中存在与肾小管周围白细胞浸润相关的肾小管外 UMOD 沉积。总之,我们确定了肾小管外的 pUMOD 是白细胞募集的一个强有力的诱导剂,强调了它在各种肾脏病理中引发炎症反应的关键作用。