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假孕大鼠蜕膜化过程中子宫内膜基质中脱氧核糖核酸合成与有丝分裂的时空模式。

Spatial and temporal patterns of deoxyribonucleic acid synthesis and mitosis in the endometrial stroma during decidualization in the pseudopregnant rat.

作者信息

Kleinfeld R G, O'Shea J D

出版信息

Biol Reprod. 1983 Apr;28(3):691-702. doi: 10.1095/biolreprod28.3.691.

Abstract

A quantitative study was made of the spatial patterns of stromal cell mitosis and DNA synthesis in the endometrium of the pseudopregnant rat before and during decidualization. A colchicine block was used for mitotic counts, and DNA synthesis was studied by [3H] thymidine autoradiography. Observations were also made on the subsequent fates of [3H] thymidine-labeled stromal cells. Before the onset of decidualization, on Days 3 and 4 (vaginal cornification = Day 0), mitosis was largely confined to the subepithelial stroma along the sides and around the antimesometrial pole of the lumen. [3H] thymidine labeling and stromal mitosis following a decidualizing stimulus at noon on Day 4 of pseudopregnancy were first seen close to the uterine lumen, with subsequent spread to deeper layers of the endometrium. At noon on Day 5, mitotic figures were numerous on all sides of the lumen and at all depths in the endometrium. At later stages, mitosis and the development of polyploidy continued in the decidual tissue, but little DNA synthesis or mitosis occurred in the basal zone of the stroma adjacent to the myometrium. In this zone, many cells in animals given [3H] thymidine 18 to 24 h after induction of decidualization remained heavily labeled throughout the growth and regression of deciduomata. Labeled cells derived from the basal zone and outer edge of the decidual capsule were present in the stroma of the regenerated endometrium following the regression of deciduomata. It was concluded that although cells at all depths in the endometrial stroma undergo DNA synthesis and mitosis in the early stages of response to a decidualizing stimulus, their subsequent behavior and fate depend upon their position in the endometrium.

摘要

对假孕大鼠蜕膜化前及蜕膜化过程中子宫内膜基质细胞有丝分裂和DNA合成的空间模式进行了定量研究。采用秋水仙碱阻断法进行有丝分裂计数,并用[3H]胸腺嘧啶核苷放射自显影术研究DNA合成。还观察了[3H]胸腺嘧啶核苷标记的基质细胞的后续命运。在蜕膜化开始前,即第3天和第4天(阴道角化=第0天),有丝分裂主要局限于沿着管腔两侧及反系膜极周围的上皮下基质。假孕第4天中午给予蜕膜化刺激后,[3H]胸腺嘧啶核苷标记和基质有丝分裂首先出现在靠近子宫管腔处,随后扩散到子宫内膜更深层。第5天中午,管腔四周及子宫内膜各深度均可见大量有丝分裂象。在后期,蜕膜组织中仍持续有有丝分裂和多倍体的发育,但与子宫肌层相邻的基质基底层几乎没有DNA合成或有丝分裂发生。在这个区域,在诱导蜕膜化后18至24小时给予[3H]胸腺嘧啶核苷的动物中,许多细胞在蜕膜瘤生长和消退的整个过程中仍有大量标记。蜕膜瘤消退后,来自蜕膜囊基底层和外缘的标记细胞存在于再生子宫内膜的基质中。得出的结论是,尽管子宫内膜基质各深度的细胞在对蜕膜化刺激的早期反应中都会经历DNA合成和有丝分裂,但它们随后的行为和命运取决于它们在子宫内膜中的位置。

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