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基底膜与致癌作用:用N-丁基-N-(4-羟丁基)亚硝胺(BBN)处理的大鼠膀胱上皮基底膜的超微结构观察

Basement membrane and carcinogenesis: ultrastructural observations in the basement membrane of the bladder epithelium in rats treated with N-butyl-N-(4-hydroxybutyl)nitrosamine (BBN).

作者信息

Zhang X, Matsuoka N, Sugimoto M, Takenaka I

机构信息

Department of Urology, Kagawa Medical School, Japan.

出版信息

Int J Urol. 1994 Jun;1(2):129-34. doi: 10.1111/j.1442-2042.1994.tb00021.x.

Abstract

This study investigated the structural alterations in the basement membrane (BM) of the bladder epithelium in rats treated with N-butyl-N-(4-hydroxybutyl)nitrosamine (BBN) using transmission electron microscopy. Following administration of BBN, thickening of the BM of the bladder epithelium was observed and remained almost constant from 4 to 20 weeks, although the pathological changes in the rat bladder epithelium induced by BBN altered over the same period of 20 weeks. The reason for this phenomenon can be explained by the increased interfacial area between the basal epithelial cells and the BM of the rat bladder epithelium due to an increase in the number and size of the microvilli on the basal cell surfaces adjacent to the BM. Our results also showed that the frequency of hemidesmosomes increased progressively during the period of carcinogenesis, especially in the lesions of noninvasive transitional cell carcinoma (TCC) in the rat bladder. It is suggested that the neosynthesis of BM components can be carried out both by benign hyperplastic cells and by noninvasive TCC cells of rat bladder. The alterations in the BM thickness may be affected by the changes in the number and size of the microvilli occurring on the basal cell surfaces adjacent to the BM. Both an increased frequency of hemidesmosomes and the neosynthesis of BM are closely related to cell proliferation during carcinogenesis.

摘要

本研究采用透射电子显微镜,研究了用N-丁基-N-(4-羟丁基)亚硝胺(BBN)处理的大鼠膀胱上皮基底膜(BM)的结构改变。给予BBN后,观察到膀胱上皮BM增厚,且在4至20周内几乎保持不变,尽管BBN诱导的大鼠膀胱上皮病理变化在同一20周期间有所改变。这种现象的原因可以解释为,与BM相邻的基底细胞表面微绒毛数量和大小增加,导致大鼠膀胱上皮基底上皮细胞与BM之间的界面面积增加。我们的结果还表明,在致癌过程中,半桥粒的频率逐渐增加,尤其是在大鼠膀胱非侵袭性移行细胞癌(TCC)病变中。提示大鼠膀胱的良性增生细胞和非侵袭性TCC细胞均可进行BM成分的新合成。BM厚度的改变可能受与BM相邻的基底细胞表面微绒毛数量和大小变化的影响。半桥粒频率增加和BM新合成均与致癌过程中的细胞增殖密切相关。

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