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蜕膜细胞的生命周期。

Life cycle of decidual cells.

作者信息

Mikhailov V M

机构信息

Institute of Cytology, Russian Academy of Sciences, St. Petersburg 194064, Russia.

出版信息

Int Rev Cytol. 2003;227:1-63. doi: 10.1016/s0074-7696(03)01007-6.

Abstract

The decisive events in the development of decidual cells (DC) are presented through examples of human and rodent decidua. Human decidua is formed by large decidual cells (LDC), endometrial granulated cells (eGC), and small decidual cells. The LDC form the main type of decidual membranes, which determine the morphological characteristics of the decidua as a tissue. Immediate precursor cells of LDC are located below the basement membrane of the uterine epithelium before and during implantation. At the next stage of differentiation, LDC acquire a spindle-like shape. Rodent LDC form an epithelium-like structure with gland properties at the terminal stage of differentiation. The single-cell structure of human decidua is a derivative of the epithelial organization of rodent decidua. Spindle-like rat LDC are characterized by a high level of protein, RNA, and DNA synthesis and by intensive proliferation. At the beginning of pregnancy, a cell proliferation predominates over cell loss. By Days 12-13 of rat pregnancy LDC loss reaches 80% per day. Terminally differentiated LDC (tLDC) disappear from decidua due to apoptosis. Apoptosis of tLDC and the exhaustion of their precursors account for the disappearance of LDC in the middle of rat pregnancy. Human term decidua is composed of living cells. Human LDC (hLDC) comprise the largest part of human decidual cells (hLDC). hLDC account for 60-90% of hDC but their relative amount can decrease to 35% in the case of significant cell loss under unfavorable conditions. A decrease of LDC is not accompanied by DC proliferation. The lack of ability of decidua to compensate for DC loss suggests DC is a growing type of cell population without cambial cells. LDC function largely by blebbing and budding. Human and rat endometrial granulated cells (eGC) are characterized by a low level of natural killer (NK) activity and a high level of natural suppressor (NS) activity. The combination of NK and NS properties is characteristic of the eGC immunoregulatory function. Other functions of decidua include control of inflammation and trophoblast growth and expansion in the uterus. The life span of decidual cells is limited by pregnancy.

摘要

通过人类和啮齿动物蜕膜的实例展示了蜕膜细胞(DC)发育过程中的决定性事件。人类蜕膜由大蜕膜细胞(LDC)、子宫内膜颗粒细胞(eGC)和小蜕膜细胞组成。LDC构成蜕膜的主要类型,决定了蜕膜作为一种组织的形态特征。LDC的直接前体细胞在植入前和植入期间位于子宫上皮基底膜下方。在分化的下一阶段,LDC呈纺锤形。啮齿动物LDC在分化末期形成具有腺体特性的上皮样结构。人类蜕膜的单细胞结构是啮齿动物蜕膜上皮组织的衍生物。纺锤形大鼠LDC的特点是蛋白质、RNA和DNA合成水平高以及增殖活跃。在怀孕初期,细胞增殖超过细胞丢失。到大鼠怀孕第12 - 13天,LDC丢失率达到每天80%。终末分化的LDC(tLDC)因凋亡而从蜕膜中消失。tLDC的凋亡及其前体细胞的耗竭导致大鼠怀孕中期LDC消失。人类足月蜕膜由活细胞组成。人类LDC(hLDC)占人类蜕膜细胞(hDC)的最大部分。hLDC占hDC的60 - 90%,但在不利条件下细胞大量丢失时,其相对数量可降至35%。LDC数量减少并不伴随DC增殖。蜕膜缺乏补偿DC丢失的能力表明DC是一种没有形成层细胞的不断增长的细胞群体。LDC主要通过出泡和出芽发挥功能。人类和大鼠子宫内膜颗粒细胞(eGC)的特点是自然杀伤(NK)活性水平低和自然抑制(NS)活性水平高。NK和NS特性的组合是eGC免疫调节功能的特征。蜕膜的其他功能包括控制炎症以及滋养层在子宫内的生长和扩展。蜕膜细胞的寿命受怀孕限制。

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