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Krüppel 样因子 5 与三聚氰胺-尿酸盐晶体诱导的大鼠肾炎有关。

Krüppel-like factor 5 associates with melamine-cyanurate crystal-induced nephritis in rats.

机构信息

Department and Institute of Physiology, National Yang-Ming University, Taipei, Taiwan.

出版信息

Nephrol Dial Transplant. 2013 Oct;28(10):2477-83. doi: 10.1093/ndt/gft308.

DOI:10.1093/ndt/gft308
PMID:24078640
Abstract

BACKGROUND

Melamine and cyanuric acid (M/CA), when orally administered together to rats, can induce crystal formation within renal tubules and cause acute kidney injury.

METHODS

To investigate the pathomechanism of crystal-induced nephritis, melamine and/or cyanuric acid were administered to 3-week-old (young) and 8-week-old (adult) rats, respectively.

RESULTS

Crystal formation, blood urea nitrogen elevation, tubular cell injury and macrophage infiltration were noted in rats fed with M/CA, but not in rats fed with vehicle, melamine or CA alone. These parameters were significantly higher in young rats than those in adult rats fed with M/CA 200 mg/kg body weight (BW) for 3 days. Krüppel-like factor 5 (KLF5) was expressed on distal tubule cells, especially when crystals deposited within the lumens. Both mRNA and protein levels were higher in young rats than those in adult rats fed with M/CA (200 mg/kg BW). KLF5 expression has been shown to modulate renal tissue cytokine production, and we found that proinflammatory cytokines like monocyte chemoattractant protein-1 and interlukin-6 were increased in kidney tissues of young rats fed with M/CA for 3 days. In contrast, interlukin-10, an anti-inflammatory cytokine, was upregulated in kidneys of adult rats fed with M/CA for 3 days.

CONCLUSIONS

Crystals are prone to deposition in distal tubules of young rats fed with M/CA. M/CA Crystal-related nephritis might be induced by the KLF5 expression, which modulated macrophage recruitment and proinflammatory cytokine production, subsequently leading to renal tubular injury and interstitial inflammation.

摘要

背景

三聚氰胺和三聚氰酸(M/CA)同时经口给予大鼠时,可在肾小管内诱导晶体形成,并导致急性肾损伤。

方法

为了研究晶体诱导肾炎的发病机制,分别给予三聚氰胺和/或三聚氰酸给 3 周龄(幼鼠)和 8 周龄(成年鼠)大鼠。

结果

M/CA 喂养的大鼠出现晶体形成、血尿素氮升高、肾小管细胞损伤和巨噬细胞浸润,但给予载体、三聚氰胺或三聚氰酸单独喂养的大鼠没有出现这些变化。与 M/CA(200mg/kg 体重)喂养的成年大鼠相比,M/CA 喂养的幼鼠上述参数显著更高,连续喂养 3 天。Krüppel 样因子 5(KLF5)在远曲小管细胞上表达,尤其是在管腔中出现晶体沉积时。M/CA(200mg/kg 体重)喂养的幼鼠和成年鼠的 mRNA 和蛋白水平均高于 M/CA 喂养的成年鼠。KLF5 的表达可调节肾脏组织细胞因子的产生,我们发现 M/CA 喂养 3 天的幼鼠肾脏组织中促炎细胞因子如单核细胞趋化蛋白-1 和白细胞介素-6 增加,而抗炎细胞因子白细胞介素-10 在 M/CA 喂养 3 天的成年鼠肾脏中上调。

结论

M/CA 喂养的幼鼠更容易在远曲小管中沉积晶体。M/CA 晶体相关肾炎可能是由 KLF5 表达诱导的,其调节巨噬细胞募集和促炎细胞因子产生,从而导致肾小管损伤和间质炎症。

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