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间质性膀胱炎和对照尿路上皮细胞基因表达谱中与分化相关的变化。

Differentiation associated changes in gene expression profiles of interstitial cystitis and control urothelial cells.

作者信息

Erickson Deborah R, Schwarze Steven R, Dixon Justin K, Clark Curtis J, Hersh Matt A

机构信息

Department of Surgery, Division of Urology, College of Medicine, University of Kentucky, Lexington, Kentucky 40536-0298, USA.

出版信息

J Urol. 2008 Dec;180(6):2681-7. doi: 10.1016/j.juro.2008.08.007. Epub 2008 Oct 31.

Abstract

PURPOSE

We evaluated gene expression profiles after inducing differentiation in cultured interstitial cystitis and control urothelial cells.

MATERIALS AND METHODS

Bladder biopsies were taken from patients with interstitial cystitis and controls, that is women undergoing surgery for stress incontinence. Primary cultures were grown in keratinocyte growth medium with supplements. To induce differentiation in some plates the medium was changed to Dulbecco's modified Eagle's minimal essential medium-F12 (Media Tech, Herndon, Virginia) with supplements. RNA was analyzed with Affymetrix(R) chips. Three patients with nonulcerative interstitial cystitis were compared with 3 controls.

RESULTS

After inducing differentiation 302 genes with a described function were altered at least 3-fold in interstitial cystitis and control cells (p <0.01). Functions of the 162 up-regulated genes included cell adhesion (eg claudins, occludin and cingulin), urothelial differentiation, the retinoic acid pathway and keratinocyte differentiation (eg skin cornified envelope components). The 140 down-regulated transcripts included genes associated with basal urothelium (eg p63, integrins beta4, alpha5 and alpha6, basonuclin 1 and extracellular matrix components), vimentin, metallothioneins, and members of the Wnt and Notch pathways. When comparing interstitial cystitis control cells after differentiation, only 7 genes with a described function were altered at least 3-fold (p <0.01). PI3, SERPINB4, CYP2C8, EFEMP2 and SEPP1 were decreased, and AKR1C2 and MKNK1 were increased in interstitial cystitis cases.

CONCLUSIONS

Differentiation associated changes occurred in interstitial cystitis and control cells. Comparing interstitial cystitis vs control cases revealed few differences. This study may have included patients with interstitial cystitis and minimal urothelial deficiency, and/or we may have selected cells that were most robust in culture. Also, the abnormal urothelium in interstitial cystitis cases may be due to post-translational changes and/or to the bladder environment.

摘要

目的

我们评估了培养的间质性膀胱炎和对照尿路上皮细胞诱导分化后的基因表达谱。

材料与方法

从间质性膀胱炎患者和对照者(即因压力性尿失禁接受手术的女性)获取膀胱活检组织。原代培养物在添加了补充剂的角质形成细胞生长培养基中生长。为了在一些培养皿中诱导分化,将培养基更换为添加了补充剂的杜氏改良伊格尔最低必需培养基-F12(Media Tech,弗吉尼亚州赫恩登)。用Affymetrix芯片分析RNA。将3例非溃疡性间质性膀胱炎患者与3例对照者进行比较。

结果

诱导分化后,间质性膀胱炎和对照细胞中302个具有已知功能的基因至少改变了3倍(p<0.01)。162个上调基因的功能包括细胞黏附(如闭合蛋白、封闭蛋白和cingulin)、尿路上皮分化、视黄酸途径和角质形成细胞分化(如皮肤角质化包膜成分)。140个下调的转录本包括与基底尿路上皮相关的基因(如p63、整合素β4、α5和α6、锌指蛋白1和细胞外基质成分)、波形蛋白、金属硫蛋白以及Wnt和Notch途径的成员。比较分化后的间质性膀胱炎对照细胞时,只有7个具有已知功能的基因至少改变了3倍(p<0.01)。在间质性膀胱炎病例中,PI3、丝氨酸蛋白酶抑制剂B4、CYP2C8、EFEMP2和硒蛋白P减少,而醛酮还原酶1C2和丝裂原活化蛋白激酶相互作用激酶1增加。

结论

间质性膀胱炎和对照细胞中发生了与分化相关的变化。比较间质性膀胱炎与对照病例发现差异很少。本研究可能纳入了间质性膀胱炎且尿路上皮缺陷最小的患者,和/或我们可能选择了培养中最健壮的细胞。此外,间质性膀胱炎病例中异常的尿路上皮可能是由于翻译后变化和/或膀胱环境所致。

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