Suppr超能文献

通过细胞化学和电子显微镜联合技术,在喂食和急性禁食小鼠的退化的、反系膜蜕膜中显示细胞外酸性磷酸酶活性。

Demonstration of extracellular acid phosphatase activity in the involuting, antimesometrial decidua in fed and acutely fasted mice by combined cytochemistry and electron microscopy.

作者信息

Katz S G

机构信息

Department of Histology, School of Medicine, Federal University of São Paulo, SP, Brazil.

出版信息

Anat Rec. 1998 Sep;252(1):1-7. doi: 10.1002/(SICI)1097-0185(199809)252:1<1::AID-AR1>3.0.CO;2-#.

Abstract

An ultrastructural cytochemical study of acid phosphatase activity in the antimesometrial decidua on days 9-11 of pregnancy was performed in fed and acutely fasted mice. Specimens were fixed in a buffered mixture of paraformaldehyde and glutaraldehyde and were incubated in a buffered medium containing sodium beta-glycerophosphate and cerium chloride for ultrastructural localization of acid phosphatase activity. Fed and fasted animals showed extracellular acid phosphatase reaction product in the decidual-trophoblast interface, in the region of loosely and tightly packed, mature decidual cells, and in the region of predecidual cells. Reaction product was absent in the region of nondecidualized stromal cells. Extracellular acid phosphatase activity was more conspicuous in the region of mature decidual cells in fasted mice than in fed mice, and it was apparently similar in the region of predecidual cells in both fed and fasted mice. Acid phosphatase reaction product was also observed in lysosomes in all cells studied. Because acid phosphatase activity reflects the presence of lysosomal hydrolases in general, our results suggest that there is matrix degradation by lysosomal enzymes in both fed and fasted mice. These events may be part of the process of tissue remodeling in regions of predecidual cells and mature decidual cells. However, it is also possible that, in the region of mature decidual cells, breakdown of matrix constituents is a mechanism to provide nutrients for the growing fetus. This mechanism is probably enhanced in fasted mice.

摘要

对妊娠第9 - 11天的小鼠子宫系膜对侧蜕膜中酸性磷酸酶活性进行了超微结构细胞化学研究,实验对象为喂食的小鼠和急性禁食的小鼠。标本用多聚甲醛和戊二醛的缓冲混合液固定,然后在含有β -甘油磷酸钠和氯化铈的缓冲培养基中孵育,以进行酸性磷酸酶活性的超微结构定位。喂食和禁食的动物在蜕膜 - 滋养层界面、松散和紧密排列的成熟蜕膜细胞区域以及前蜕膜细胞区域均显示出细胞外酸性磷酸酶反应产物。未蜕膜化的基质细胞区域没有反应产物。禁食小鼠成熟蜕膜细胞区域的细胞外酸性磷酸酶活性比喂食小鼠更明显,而喂食和禁食小鼠的前蜕膜细胞区域的活性显然相似。在所有研究的细胞的溶酶体中也观察到了酸性磷酸酶反应产物。由于酸性磷酸酶活性总体上反映了溶酶体水解酶的存在,我们的结果表明,喂食和禁食的小鼠中均存在溶酶体酶介导的基质降解。这些事件可能是前蜕膜细胞和成熟蜕膜细胞区域组织重塑过程的一部分。然而,在成熟蜕膜细胞区域,基质成分的分解也可能是为生长中的胎儿提供营养的一种机制。这种机制在禁食小鼠中可能会增强。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验