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晶体诱导的肾脏炎症:来自人体研究、动物模型和组织培养研究的结果。

Crystal-induced inflammation of the kidneys: results from human studies, animal models, and tissue-culture studies.

作者信息

Khan Saeed R

机构信息

Department of Pathology, College of Medicine, University of Florida, Gainesville, FL 32610-0275, USA.

出版信息

Clin Exp Nephrol. 2004 Jun;8(2):75-88. doi: 10.1007/s10157-004-0292-0.

Abstract

Calcium oxalate (CaOx), calcium phosphate (CaP), and uric acid or urate are the most common crystals seen in the kidneys. Most of the crystals evoke an inflammatory response leading to fibrosis, loss of nephrons, and eventually to chronic renal failure. Of the three, CaOx monohydrate is the most reactive, whereas some forms of CaP do not evoke any discernible response. Reactive oxygen species are produced during the interactions between the crystals and renal cells and are responsible for the various cellular responses. CaOx crystals generally form in the renal tubules. Exposure of renal epithelial cells to CaOx crystals results in the increased synthesis of osteopontin, bikunin, heparan sulfate, monocyte chemoattractant protein 1 (MCP-1), and prostaglandin (PG) E2, which are known to participate in inflammatory processes and in extracellular matrix production. CaOx crystal deposition in rat kidneys also activates the renin-angiotensin system. Both Ox and CaOx crystals selectively activate p38 mitogen-activated protein kinase (MAPK) in exposed tubular cells. CaP crystals can form in the tubular lumen, tubular cells, or tubular basement membrane. Renal epithelial cells exposed to brushite crystals produce MCP-1. Basic CaP and calcium pyrophosphate dihydrate induce mitogenesis in fibroblasts, stimulate production of PGE2, and up-regulate the synthesis of metalloproteinases (MMP) while down-regulating the production of inhibitors of MMPs through activation of p42/44 MAPK. Deposition of urate crystals in the kidneys becomes associated with renal tubular atrophy, interstitial fibrosis, and development of inflammatory infiltrate. Renal epithelial cells exposed to uric acid crystals synthesize MCP-1 as well as PGE2. Monocytes or neutrophils exposed to urate crystals produce tumor necrosis factor alpha, interleukin-1 (IL-1), IL-6, and IL-8. Expression of IL-8 is mediated through extracellular signal-regulated kinase 1 (ERK-1)/ERK-2 and nuclear transcription factors activated protein 1 and nuclear factor kappabeta. Urate crystals also stimulate the macrophages to produce MMPs.

摘要

草酸钙(CaOx)、磷酸钙(CaP)以及尿酸或尿酸盐是在肾脏中最常见的晶体。大多数晶体引发炎症反应,导致纤维化、肾单位丧失,并最终发展为慢性肾衰竭。在这三种晶体中,一水合草酸钙反应性最强,而某些形式的磷酸钙则不会引发任何可察觉的反应。活性氧物种在晶体与肾细胞的相互作用过程中产生,并负责各种细胞反应。草酸钙晶体通常在肾小管中形成。肾上皮细胞暴露于草酸钙晶体后,骨桥蛋白、 bikunin、硫酸乙酰肝素、单核细胞趋化蛋白1(MCP-1)和前列腺素(PG)E2的合成增加,这些物质已知参与炎症过程和细胞外基质的产生。草酸钙晶体在大鼠肾脏中的沉积也会激活肾素 - 血管紧张素系统。草酸(Ox)和草酸钙晶体都会在暴露的肾小管细胞中选择性激活p38丝裂原活化蛋白激酶(MAPK)。磷酸钙晶体可在肾小管腔、肾小管细胞或肾小管基底膜中形成。暴露于透钙磷石晶体的肾上皮细胞会产生MCP-1。碱性磷酸钙和二水合焦磷酸钙可诱导成纤维细胞有丝分裂,刺激前列腺素E2的产生,并上调金属蛋白酶(MMP)的合成,同时通过激活p42/44 MAPK下调MMP抑制剂的产生。尿酸盐晶体在肾脏中的沉积与肾小管萎缩、间质纤维化以及炎症浸润的发展有关。暴露于尿酸晶体的肾上皮细胞会合成MCP-1以及前列腺素E2。暴露于尿酸晶体的单核细胞或中性粒细胞会产生肿瘤坏死因子α、白细胞介素-1(IL-1)、IL-6和IL-8。IL-8的表达是通过细胞外信号调节激酶1(ERK-1)/ERK-2以及核转录因子活化蛋白1和核因子κB介导的。尿酸盐晶体还会刺激巨噬细胞产生金属蛋白酶。

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