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肿瘤坏死因子促进神经源性膀胱炎中膀胱肥大细胞的差异性转运。

Tumor necrosis factor promotes differential trafficking of bladder mast cells in neurogenic cystitis.

作者信息

Chen Michael C, Blunt Lynn W, Pins Michael R, Klumpp David J

机构信息

Department of Urology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

出版信息

J Urol. 2006 Feb;175(2):754-9. doi: 10.1016/S0022-5347(05)00171-0.

Abstract

PURPOSE

IC is often considered neurogenic cystitis, in which mast cells are involved in a positive feedback loop that results in sustained urothelial inflammation. To characterize these processes we developed a murine model of neurogenic cystitis using Bartha's strain of PRV based on a similar model in the rat.

MATERIALS AND METHODS

Female C57BL/6 mice (National Cancer Institute, Bethesda, Maryland) were used in the study. Neurogenic cystitis was induced by the injection of Bartha's strain of PRV (2.2 x 10 pfu) into the abductor caudalis dorsalis tail base muscle. Bladder inflammation was assessed by leukocyte influx and Evans blue dye extravasation. Mast cells were visualized in bladder tissue by staining with 0.1% toluidine blue.

RESULTS

Inoculation with PRV in the abductor caudalis dorsalis resulted in cystitis within 3 days. Coincident with the induction of cystitis mast cells accumulated in the lamina propria due to mast cell trafficking from the proximal detrusor (relative to the lumen), whereas mast cells from the distal detrusor were unchanged and total mast cell counts were not increased. Degranulated mast cells increased approximately 20-fold in the lamina propria of infected mice relative to controls. In TNF receptor 1/2 deficient mice (Jackson Laboratory, Bar Harbor, Maine) mast cell trafficking was not observed in response to PRV and mast cells were not degranulated.

CONCLUSIONS

These data indicate that neurogenic cystitis is associated with the differential trafficking and activation of distinct mast cell pools in the bladder. Since TNF mediates these events, anti-TNF therapy may mitigate the pathogenesis of neurogenic cystitis.

摘要

目的

间质性膀胱炎(IC)常被认为是神经源性膀胱炎,其中肥大细胞参与了导致膀胱上皮持续炎症的正反馈回路。为了表征这些过程,我们基于大鼠的类似模型,利用巴瑟株伪狂犬病病毒(PRV)开发了一种神经源性膀胱炎小鼠模型。

材料与方法

本研究使用雌性C57BL/6小鼠(美国国立癌症研究所,马里兰州贝塞斯达)。通过将巴瑟株PRV(2.2×10噬斑形成单位)注射到尾背侧外展肌来诱导神经源性膀胱炎。通过白细胞流入和伊文思蓝染料外渗评估膀胱炎症。用0.1%甲苯胺蓝对膀胱组织进行染色以观察肥大细胞。

结果

在尾背侧外展肌接种PRV后3天内引发膀胱炎。与膀胱炎的诱导同时发生的是,由于肥大细胞从逼尿肌近端(相对于管腔)迁移,固有层中肥大细胞积聚,而逼尿肌远端的肥大细胞未发生变化,肥大细胞总数也未增加。相对于对照组,感染小鼠固有层中脱颗粒的肥大细胞增加了约20倍。在肿瘤坏死因子受体1/2缺陷小鼠(缅因州巴尔港杰克逊实验室)中,未观察到对PRV的肥大细胞迁移反应,肥大细胞也未脱颗粒。

结论

这些数据表明神经源性膀胱炎与膀胱中不同肥大细胞池的差异迁移和激活有关。由于肿瘤坏死因子介导这些事件,抗肿瘤坏死因子治疗可能减轻神经源性膀胱炎的发病机制。

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