Elevated Expressions of 15-Lipoxygenase and Lipoxin A4 in Children with Acute Poststreptococcal Glomerulonephritis

被引:51
作者
Wu, Sheng-Hua [1 ]
Liao, Pei-Yuan
Yin, Pei-Ling [2 ]
Zhang, Yong-Mei [1 ]
Dong, Ling [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Pediat, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Nanjing Hosp Affiliated 1, Dept Pediat, Nanjing, Peoples R China
关键词
RAT MESANGIAL CELLS; HUMAN-NEUTROPHILS; INFLAMMATION; LEUKOTRIENE-B4; TRANSFORMATION; TRAFFICKING; NEPHRITIS; RESPONSES; KIDNEY; ANALOG;
D O I
10.2353/ajpath.2009.080671
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Anti-inflammatory effects of the 15-lipoxygenase (15-LO) derivatives lipoxin A(4) (LXA(4)) and 15-S-hydroxy-eicosatetraenoic acid (15-S-HETE) have been documented in many experimental models of acute inflammation. However, the expression levels of 15-LO and its products in human renal diseases remain unknown. This study investigated the expression levels of LXA(4,) leukotriene B-4 (LTB4), and 15-LO in leukocytes and glomeruli obtained from 22 children with acute poststreptococcal glomerulonephritis (APSGN), and determined the modulatory effects of both 15-S-HETE and LXA(4) on LTB4 synthesis in leukocytes and LTB4-evoked chemotaxis of polymorphonuclear leukocytes (PMNs) obtained from children during the first 3 days after onset of APSGN. Expression levels of both LXA4 and 15-LO in leukocytes; and glomeruli were up-regulated during the acute phase of disease, further peaking between days 10 and 14, and remained increased after 6 to 8 weeks of APSGN onset. In contrast, blood and urinary levels of LTB4 as well as the number of glomerular PMNs peaked during the acute phase of disease and then decreased during the resolution phase. Administration of both 15-S-HETE and LXA4 in vitro inhibited LTB4-induced chemotaxis of PMNs and production of LTB4 from leukocytes obtained from patients with APSGN. The current study provides further support for an anti-inflammatory role for 15-LO products in human nephritis through both antagonism and inhibition of leukotriene synthesis and its biological activity. (Am J Pathol 2009, 174:115-122; DOI.10.2353/ajpath.2009.080671)
引用
收藏
页码:115 / 122
页数:8
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