Kashiwagi Emi, Tonomura Yutaka, Kondo Chiaki, Masuno Koichi, Fujisawa Kae, Tsuchiya Noriko, Matsushima Shuuichi, Torii Mikinori, Takasu Nobuo, Izawa Takeshi, Kuwamura Mitsuru, Yamate Jyoji
Developmental Research Laboratories, Shionogi & Co., Ltd., 3-1-1 Futaba-cho, Toyonaka, Osaka 561-0825, Japan; Laboratories of Veterinary Pathology, Life and Environmental Sciences, Osaka Prefecture University, Rinkuu Ourai Kita 1-58, Izumisano-shi, Osaka 598-8531, Japan.
Developmental Research Laboratories, Shionogi & Co., Ltd., 3-1-1 Futaba-cho, Toyonaka, Osaka 561-0825, Japan.
Exp Toxicol Pathol. 2014 Sep;66(7):301-11. doi: 10.1016/j.etp.2014.04.007. Epub 2014 Jun 7.
The kidney has a capacity to recover from ischemic or toxic insults that result in cell death, and timely tissue repair of affected renal tubules may arrest progression of injury, leading to regression of injury and paving the way for recovery. To investigate the roles of neutrophil gelatinase-associated lipocalin (NGAL/lcn2) and osteopontin (OPN/spp1) during renal regeneration, the expression patterns of NGAL and OPN in the cisplatin-induced rat renal failure model were examined. NGAL expression was increased from day 1 after injection; it was seen mainly in the completely regenerating proximal tubules of the cortico-medullary junction on days 3-35; however, the expression was not seen in abnormally dilated or atrophied renal tubules surrounded by fibrotic lesions. On the other hand, OPN expression was increased from day 5 and the increased expression developed exclusively in the abnormal renal tubules. NGAL expression level well correlated with the proliferating activity in the regenerating renal epithelial cells, whereas OPN significantly correlated with the α-smooth muscle actin-positive myofibroblast appearance, expression of transforming growth factor (TGF)-β1, and the number of CD68-positive macrophages. Interestingly, rat renal epithelial cell line (NRK-52E) treated with TGF-β1 decreased NGAL expression, but increased OPN expression in a dose-dependent manner. Because increases of TGF-β1, myofibroblasts and macrophages contribute to progressive interstitial renal fibrosis, OPN may be involved in the pathogenesis of fibrosis; on the contrary, NGAL may play a role in tubular regeneration after injury. Expression analysis of NGAL and OPN would be useful to investigate the tubule damage in renal-toxicity.
肾脏具有从导致细胞死亡的缺血或毒性损伤中恢复的能力,受影响肾小管的及时组织修复可能会阻止损伤进展,导致损伤消退并为恢复铺平道路。为了研究中性粒细胞明胶酶相关脂质运载蛋白(NGAL/lcn2)和骨桥蛋白(OPN/spp1)在肾脏再生过程中的作用,我们检测了顺铂诱导的大鼠肾衰竭模型中NGAL和OPN的表达模式。注射后第1天NGAL表达增加;在第3至35天主要见于皮质-髓质交界处完全再生的近端小管;然而,在被纤维化病变包围的异常扩张或萎缩的肾小管中未见该表达。另一方面,OPN表达从第5天开始增加,且增加的表达仅在异常肾小管中出现。NGAL表达水平与再生肾上皮细胞的增殖活性密切相关,而OPN与α-平滑肌肌动蛋白阳性肌成纤维细胞的出现、转化生长因子(TGF)-β1的表达以及CD68阳性巨噬细胞的数量显著相关。有趣的是,用TGF-β1处理的大鼠肾上皮细胞系(NRK-52E)降低了NGAL表达,但以剂量依赖方式增加了OPN表达。由于TGF-β1、肌成纤维细胞和巨噬细胞的增加促成了进行性间质性肾纤维化,OPN可能参与了纤维化的发病机制;相反,NGAL可能在损伤后的肾小管再生中发挥作用。NGAL和OPN的表达分析将有助于研究肾毒性中的肾小管损伤。