Elevated levels of miR-146a and miR-155 in kidney biopsy and urine from patients with IgA nephropathy
Elevated levels of miR-146a and miR-155 in kidney biopsy and urine from patients with IgA nephropathy
复制标题
IgA 肾病患者肾活检和尿液中 miR-146a 和 miR-155 水平升高
DOI:
10.1155/2011/304852
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发表时间:
2011-01-01
期刊:
影响因子:
--
通讯作者:
Szeto, Cheuk-Chun
中科院分区:
文献类型:
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作者:
Wang, Gang;Kwan, Bonnie Ching-Ha;Szeto, Cheuk-Chun
Background: Previous studies suggested miR-146a and miR-155 play important roles in innate and adaptive immune responses. We studied intra-renal and urinary levels of miR-146a and miR-155 in patients with immunoglobulin A nephropathy (IgAN).Methods: Intra-renal and urinary levels of miR-146a and miR-155 are quantified in 43 patients with IgAN; the result was compared to 20 nephrectomy specimens and urine sediment of 13 healthy volunteers.Results: The levels of intra-renal and urinary levels of miR-146a and miR-155 of IgAN are significantly higher than controls. Estimated glomerular filtration rate inversely correlates with intra-renal level of miR-146a and miR-155; proteinuria positively correlates with intra-renal level of miR-146a and miR-155. as well as urinary level of miR-146a and miR-155. Intra-renal level of miR-155 significantly correlates with tubulointerstitial scarring. Urinary level of miR-146a inversely correlates with urinary expression of interleukin (IL)-1 beta, IL-6 and tumor necrosis factor (TNF)-alpha and positively correlates with urinary expression of regulated upon activation, normal T-cell expressed, and secreted (RANTES). Urinary level of miR-155 inversely correlates with urinary expression of IL-1 beta and TNF-alpha and positively correlates with urinary expression of forkhead box P3 (FOXP3) and RANTES.Conclusion: We conclude that intra-renal and urinary levels of miR-146a and miR-155 were significantly elevated in IgAN, and the degree of upregulation correlates with clinical and histological severity of the disease. Our results suggested miR-146a and miR-155 might play an important role in the pathophysiology of IgAN.