Suppr超能文献

通过对铁蓄积的抗性鉴定致癌物诱导的肝细胞改变灶中的超微结构异常。

Ultrastructural abnormalities in carcinogen-induced hepatocellular altered foci identified by resistance to iron accumulation.

作者信息

Hirota N, Williams G M

出版信息

Cancer Res. 1982 Jun;42(6):2298-309.

PMID:7074612
Abstract

Hepatocellular altered foci were induced in rat liver by cycles of feeding of N-2-fluorenylacetamide and were distinguished by their resistance to iron accumulation following production of hepatic siderosis by dietary administration of 8-hydroxyquinoline and ferrous gluconate. The foci were readily identified by their iron exclusion in plastic-embedded sections stained for iron. Sections from iron-free regions processed for electron microscopy permitted ultrastructural study of cells in foci identified by reduced cytoplasmic ferritin. Altered foci of the eosinophilic type produced by cyclic feeding of carcinogen for 16 weeks were composed of both normal-appearing hepatocytes and others with ultrastructural abnormalities, including increased agranular reticulum with associated glycogen particles, decreased rough endoplasmic reticulum with reduced length of cisternae, degranulated rough vesicles, altered and displaced Golgi complexes, and abnormal bile canaliculi. At 12 and 24 weeks after cessation of carcinogen exposure, cells in persistent eosinophilic foci continued to display ultrastructural abnormalities. They possessed increased rough endoplasmic reticulum with rather regular cisternal arrangement and relatively increased smooth endoplasmic reticulum. Golgi complexes were abnormal. Bile canaliculi were abnormal and occasionally increased in number. Nuclei displayed prominent nucleoli. Cells in a basophilic focus were characterized by the presence of numerous free polyribosomes diffusely scattered throughout the cytoplasm, distended rough endoplasmic reticulum with loss of parallel-stack and hypertrophic dilated Golgi complexes, and prominent marginated nucleoli. The finding that persistent foci continued to display ultrastructural abnormalities, some of which changed or progressed in the absence of further carcinogen exposure, suggests that the persistent iron-excluding foci are a permanently altered population.

摘要

通过喂食N-2-芴基乙酰胺诱导大鼠肝脏产生肝细胞改变灶,并通过在饮食中给予8-羟基喹啉和葡萄糖酸亚铁产生肝铁沉积后,这些病灶对铁积累具有抗性来加以区分。在经铁染色的塑料包埋切片中,这些病灶因铁排斥而易于识别。对无铁区域进行电子显微镜处理的切片,允许对通过细胞质铁蛋白减少而鉴定出的病灶中的细胞进行超微结构研究。通过致癌物循环喂食16周产生的嗜酸性类型的改变灶,由外观正常的肝细胞和其他具有超微结构异常的细胞组成,包括无颗粒内质网增加并伴有相关糖原颗粒、粗面内质网减少且池长度缩短、粗面小泡脱颗粒、高尔基体复合体改变和移位以及胆小管异常。在停止致癌物暴露后12周和24周,持续性嗜酸性病灶中的细胞继续表现出超微结构异常。它们具有增加的粗面内质网,其池排列相当规则,并且滑面内质网相对增加。高尔基体复合体异常。胆小管异常,数量偶尔增加。细胞核显示出明显的核仁。嗜碱性病灶中的细胞特征是在整个细胞质中弥漫性散布着大量游离多聚核糖体、粗面内质网扩张且失去平行堆叠以及高尔基体复合体肥大扩张,并且有明显的边缘核仁。持续性病灶继续表现出超微结构异常,其中一些在没有进一步致癌物暴露的情况下发生改变或进展,这一发现表明持续性铁排斥病灶是一个永久改变的群体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验