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雌激素受体β缺陷的雌性小鼠会出现类似人类间质性膀胱炎的膀胱表型。

Estrogen receptor beta-deficient female mice develop a bladder phenotype resembling human interstitial cystitis.

作者信息

Imamov Otabek, Yakimchuk Konstantin, Morani Andrea, Schwend Thomas, Wada-Hiraike Osamu, Razumov Sergei, Warner Margaret, Gustafsson Jan-Ake

机构信息

Department of Biosciences and Nutrition, Karolinska Institute, Novum, SE-141 86 Stockholm, Sweden.

出版信息

Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9806-9. doi: 10.1073/pnas.0703410104. Epub 2007 May 23.

Abstract

Interstitial cystitis/painful bladder syndrome is a disease seen mostly in women, and symptoms tend to be worse premenopausally or during ovulation. The four cardinal symptoms of interstitial cystitis/painful bladder syndrome are bladder pain, urgency, frequency, and nocturia. Estrogen has been implicated in the etiology of this disease, but the role of the two estrogen receptors (ER), ERalpha and ERbeta, has not been investigated. We found that, in the bladders of WT mice, ERbeta is expressed in the basal cell layer of the urothelium. Bladders of male ERbeta(-/-) mice were intact and morphologically indistinguishable from those of their WT littermates. However, in female ERbeta(-/-) mice, there was ulceration and atrophy of bladder urothelium concomitant with infiltration of gammadelta T cells concentrated in the areas of atrophy and shedding of urothelium. The data support the idea that activated gammadelta T cells are causing the damage to the urothelium. The hyperactivity of T cells may be because of an imbalance between ERalpha and ERbeta signaling in female ERbeta(-/-) mice. Our data suggest that reduced ERbeta signaling might have a role in the pathogenesis of interstitial cystitis, and ERbeta could be a candidate for a target of medical therapy.

摘要

间质性膀胱炎/膀胱疼痛综合征是一种多见于女性的疾病,其症状在绝经前或排卵期间往往会加重。间质性膀胱炎/膀胱疼痛综合征的四大主要症状是膀胱疼痛、尿急、尿频和夜尿症。雌激素被认为与该疾病的病因有关,但两种雌激素受体(ER),即雌激素受体α(ERα)和雌激素受体β(ERβ)的作用尚未得到研究。我们发现,在野生型(WT)小鼠的膀胱中,ERβ表达于尿路上皮的基底细胞层。雄性ERβ基因敲除(ERβ(-/-))小鼠的膀胱完好无损,在形态上与同窝野生型小鼠的膀胱没有区别。然而,在雌性ERβ(-/-)小鼠中,膀胱尿路上皮出现溃疡和萎缩,同时γδ T细胞浸润,这些细胞集中在尿路上皮萎缩和脱落的区域。这些数据支持活化的γδ T细胞正在损伤尿路上皮这一观点。T细胞的过度活跃可能是由于雌性ERβ(-/-)小鼠中ERα和ERβ信号之间的失衡。我们的数据表明,ERβ信号的减少可能在间质性膀胱炎的发病机制中起作用,并且ERβ可能是药物治疗靶点的一个候选对象。

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