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本文引用的文献

1
Analysis of apoptotic cell death, Bcl-2, and p53 protein expression in freshly fixed and cryopreserved ovarian tissue after exposure to warm ischemia.暴露于热缺血后,新鲜固定和冷冻保存的卵巢组织中凋亡细胞死亡、Bcl-2和p53蛋白表达的分析
Fertil Steril. 2006 Apr;85 Suppl 1:1082-92. doi: 10.1016/j.fertnstert.2005.10.020.
2
Expression of Fas, Bcl-2 and p53 molecules in glomerulonephritis and their correlations with clinical and laboratory findings.Fas、Bcl-2和p53分子在肾小球肾炎中的表达及其与临床和实验室检查结果的相关性。
Nephrology (Carlton). 2005 Jun;10(3):311-6. doi: 10.1111/j.1440-1797.2005.00397.x.
3
Apoptosis in the ovary: molecular mechanisms.卵巢中的细胞凋亡:分子机制
Hum Reprod Update. 2005 Mar-Apr;11(2):162-77. doi: 10.1093/humupd/dmi001. Epub 2005 Feb 10.
4
[Serum level and urinary excretion of soluble Fas (sFas) in patients with primary glomerulopathies].[原发性肾小球疾病患者血清可溶性Fas(sFas)水平及尿排泄情况]
Pol Arch Med Wewn. 2002 Sep;108(3):843-7.
5
Apoptosis and melanoma: molecular mechanisms.细胞凋亡与黑色素瘤:分子机制
J Pathol. 2003 Mar;199(3):275-88. doi: 10.1002/path.1300.
6
A shift in the Bax/Bcl-2 balance may activate caspase-3 and modulate apoptosis in experimental glomerulonephritis.
Kidney Int. 2002 Oct;62(4):1301-13. doi: 10.1111/j.1523-1755.2002.kid587.x.
7
Immunopathogenesis of lupus and lupus nephritis: recent insights.狼疮及狼疮性肾炎的免疫发病机制:最新见解
Curr Opin Nephrol Hypertens. 2002 May;11(3):273-7. doi: 10.1097/00041552-200205000-00002.
8
Relationship of oncogenes (sFas, Bcl-2) and cytokines (IL-10, alfa-TNF) with the activity of systemic lupus erythematosus.癌基因(sFas、Bcl-2)和细胞因子(IL-10、α-TNF)与系统性红斑狼疮活动度的关系。
Anticancer Res. 2001 Jul-Aug;21(4B):3053-9.
9
Apoptosis in different cutaneous manifestations of lupus erythematosus.红斑狼疮不同皮肤表现中的细胞凋亡
Br J Dermatol. 2001 May;144(5):958-66. doi: 10.1046/j.1365-2133.2001.04182.x.
10
Fas-Fas ligand system in the peripheral blood of patients with renal diseases.肾病患者外周血中的Fas-Fas配体系统
Nephron. 2000 Jun;85(2):107-13. doi: 10.1159/000045642.

狼疮性肾炎中肾小球的表达及血清Bcl-2和Fas蛋白升高:初步研究结果。

Glomerular expression and elevated serum Bcl-2 and Fas proteins in lupus nephritis: preliminary findings.

作者信息

Fathi N A, Hussein M R, Hassan H I, Mosad E, Galal H, Afifi N A

机构信息

Department of Rheumatology and Rehabilitation, Faculty of Medicine and Assuit University Hospitals, Assuit, Egypt.

出版信息

Clin Exp Immunol. 2006 Nov;146(2):339-43. doi: 10.1111/j.1365-2249.2006.03219.x.

DOI:10.1111/j.1365-2249.2006.03219.x
PMID:17034587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1942057/
Abstract

Programmed cell death (apoptosis) is involved in glomerular injuries leading to glomerulonephritis. Bcl-2 and Fas are proteins that promote cell survival and death, respectively. This study tests the hypothesis that lupus nephritis is associated with alterations of Bcl-2 and Fas protein expression. Thirty-six patients with lupus nephritis and 10 controls (normal individuals) were included in this study. Bcl-2 and Fas positive cells were examined in kidney biopsies by immunohistochemistry. Bcl-2 and Fas serum levels were evaluated by enzyme-linked immunosorbent assay (ELISA). In the glomeruli of normal kidneys, Bcl-2 and Fas proteins were completely absent. In lupus nephritis patients, glomerular expression of Bcl-2 and Fas was seen in mesangial cells (1.3 +/- 0.1 and 2.0 +/- 0.1 for Bcl-2 and Fas, respectively). Similarly, a statistically significantly higher Bcl-2 (217.1 +/- 85.9) and Fas (767.9 +/- 271) serum levels were found in lupus patients compared to controls (148.6 +/- 87, 550.3 +/- 91 for Bcl-2 and Fas, P < 0.05). A direct correlation between serum Bcl-2 and Fas and chronicity index was also found. Compared to normal controls, lupus nephritis is associated with glomerular expression and elevated serum levels of Bcl-2 and Fas proteins. These findings suggest possible roles for Bcl-2 and Fas in glomerular injury during evolution of lupus nephritis. The diagnostic, prognostic and therapeutic ramifications of our findings are open to further investigation.

摘要

程序性细胞死亡(凋亡)参与导致肾小球肾炎的肾小球损伤。Bcl-2和Fas分别是促进细胞存活和死亡的蛋白质。本研究检验狼疮性肾炎与Bcl-2和Fas蛋白表达改变相关的假说。本研究纳入了36例狼疮性肾炎患者和10例对照(正常个体)。通过免疫组织化学检查肾活检组织中的Bcl-2和Fas阳性细胞。通过酶联免疫吸附测定(ELISA)评估Bcl-2和Fas血清水平。在正常肾脏的肾小球中,完全不存在Bcl-2和Fas蛋白。在狼疮性肾炎患者中,在系膜细胞中可见Bcl-2和Fas的肾小球表达(Bcl-2和Fas分别为1.3±0.1和2.0±0.1)。同样,与对照组相比,狼疮患者的Bcl-2(217.1±85.9)和Fas(767.9±271)血清水平在统计学上显著更高(Bcl-2和Fas分别为148.6±87、550.3±91,P<0.05)。还发现血清Bcl-2和Fas与慢性指数之间存在直接相关性。与正常对照相比,狼疮性肾炎与Bcl-2和Fas蛋白的肾小球表达及血清水平升高相关。这些发现提示Bcl-2和Fas在狼疮性肾炎进展过程中的肾小球损伤中可能发挥作用。我们研究结果的诊断、预后和治疗意义有待进一步研究。