期刊文献+

肝移植术后稳定生存者外周血中差异表达miRNA及其功能预测 被引量:2

Differential expressions of microRNAs and their predicted targets in liver transplant recipients with long-term stable survival
下载PDF
导出
摘要 目的寻找肝移植术后长期稳定生存者外周血中有意义的生物学标志物。方法纳入肝移植术后稳定存活患者29例(STA组),反复排斥反应者10例(RJ组),健康对照者17例(HC组),利用芯片检测各组PBMCs中micro RNAs的表达谱,并用Real-time PCR对差异表达的micro RNAs进行验证。结果芯片结果显示STA组对比于RJ组共13个micro RNA表达明显下调,经Real-time PCR验证3个micro RNA(mi R-106b,mi R-18b,mi R-340)表达下调。结论肝移植患者外周血mi R-106b、mi R-18b、mi R-340可作为肝移植术后潜在标志物。 Objective To determine whether the mi RNA expression profile in peripheral blood mononuclear cells(PBMCs)differs between liver transplant recipients with long-term stable survival and those with acute rejection. Methods Twenty-nine liver transplant recipients with long-term stable survival(STA) group, 10 recipients with acute rejection(RJ group), and 17 healthy subjects(control group) were recruited for genome-wide microarray analysis of mi RNA expressions in the PBMCs.The differentially expressed mi RNAs among the 3 groups were validated by real-time PCR, and the targets of these mi RNAs were predicted. Results Compared with the RJ group, the STA group showed down-regulation of 13 mi RNAs in the PBMCs.Of these down-regulated mi RNAs, mi RNA-18 b, mi RNA-340 and mi RNA-106 b were validated by real-time PCR, and the latter two mi RNAs were predicted to target the TGF-β pathway. Conclusions The differentially expressed mi RNAs in liver transplant recipients with long-term stable survival, namely mi RNA-18 b, mi RNA-340 and mi RNA-106 b, can be potential clinical biomarkers to predict the outcomes of liver transplantation.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2015年第11期1557-1563,共7页 Journal of Southern Medical University
基金 高等学校博士学科点专项科研基金资助项目(博导)(20120171110073)
关键词 MIRNA 生物标志物 肝移植 免疫耐受 排斥反应 miRNA biomarkers liver transplantation long-term survival acute rejection
  • 相关文献

参考文献48

  • 1Turka LA, Wood K, Bluestone JA. Bringing transplantation tolerance into the clinic: lessons from the ITN and RISET for the Establishment of Tolerance consortia [ J]. Curr Opin Organ Transplant, 2010, 15(4): 441-8.
  • 2Lerut J, Sanchez-Fueyo A. An appraisal of tolerance in liver transplantation[J]. Am J Transplant, 2006, 6(8): 1774-80.
  • 3Koshiba T, Li Y, Takemura M, et al. Clinical, immunological, and pathological aspects of operational tolerance after pediatric living-donor liver transplantation[J]. Transpl Immunol, 2007, 17(2): 94-7.
  • 4Martinez-Llordella M, Puig-Pey I, Orlando G, et al. Multiparameter immune profiling of operational tolerance in liver transplantation [J]. Am J Transplant, 2007, 7(2): 309-19.
  • 5Martinez-Llordella M, Lozano J J, Puig-Pey 1, et al. Using transcriptional profiling to develop a diagnostic test of operational tolerance in liver transplant recipients [J]. J Clin Invest, 2008, 118 (8): 2845-57.
  • 6Tryphonopoulos P, Ruiz P, Weppler D, et al. Long-term follow-up of 23 operational tolerant liver transplant recipients [J]. Transpl- antation, 2010, 90(12): 1556-61.
  • 7Nafady-Hego H, Li Y, Ohe H, et al. The Generation of donor- specific CD4^+CD25^+CD45RA^+ naive regulatory T cells in opera- tionally tolerant patients after pediatric living-donor liver transpl- antation[J]. Transplantation, 2010, 90(12): 1547-55.
  • 8Charlton MR, Wall WJ, Ojo AO, et al. Report of the first international liver transplantation society expert panel consensus conference on renal insufficiency in liver transplantation [J]. Liver Transpl, 2009, 15(11): S1-34.
  • 9Turka LA, Lechler RI. Towards the identification of biomarkers of transplantation tolerance[J]. Nat Rev Immunol, 2009, 9(7): 521-6.
  • 10O'connell RM, Rao DS, Chaudhuri AA, et al. Physiological and pathological roles for microRNAs in the immune system [J]. Nat Rev Immunol, 2010, 10(2): 111-22.

同被引文献23

  • 1Bouchard J, Aeharya A, Cerda J, et al. A prospective in- ternational multicenter study of AKI in the intensive care Unit[J]. Clin J Am Soc Nephrol,2015,10(8): 1324-1331.
  • 2Hoste EA, Bagshaw SM, Bellomo R, et al. Epidemiology of acute kidney injury in critically ill patients:The multina- tional AKI-EPI study[J]. Intensive Care Med, 2015,41 (8) : 1411-1423.
  • 3Khwaja A. KDIGO clinical practice guidelines for acute kidney injury[J]. Nephron Clin Pract,2012,120(4):c179- c184.
  • 4Meersch M,Schmidt C,Van Aken H,et al. Validation of cell-cycle arrest biomarkers for acute kidney injury after pediatric cardiac surgery[l]. PLo S One, 2014,9(10) :el 10865.
  • 5Endre ZH,Pickering JW. Acute kidney injury: Cell cycle arrest biomarkers win race for AKI diagnosis[J]. Nat Rev Nephrol, 2014,10(12) : 683-685.
  • 6Iwakura T,Fujigaki Y,Fujikura T,et al. Acquired resis- tance to rechallenge injury after acute kidney injury in rats is associated with cell cycle arrest in proximal tubule cells[J]. Am J Physiol Renal Physiol, 2016,3 l0 (9) : F872- F884.
  • 7Bell M, Larsson A, Venge P, et al. Assessment of cell-cy- cle arrest biomarkers to predict early and delayed acute kidney injury[]]. Dis Markers, 2015,2015 : 158658.
  • 8Azzalini L,Spagnoli V,Ly HQ. Contrast-induced nephropa- thy: From pathophysiology to preventive strategies[J]. ,Can J Cardiol,2016, 32(2) :247-255.
  • 9Molitoris BA. Therapeutic translation in acute kidney in- jury:The epithelial/endothelial axis[J]. J Clin Invest,2014, 124(6) : 2355-2363.
  • 10Keir I,Kellum JA. Acute kidney injury in severe sepsis: Pathophysiology,diagnosis,and treatment recommenda- tions[J]. J Vet Emerg Crit Care, 2015,25 (2) :200,209.

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部