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大鼠子宫基质中的细胞组织。II. 去卵巢大鼠对孕酮的反应。

Cell organization in the stroma of the rat uterus. II. Responses to progesterone in the ovariectomised rat.

作者信息

Rogers A W, Wischik C M

出版信息

J Anat. 1983 Oct;137 (Pt 3)(Pt 3):541-53.

PMID:6418698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1171847/
Abstract

The organisation and activity of cells in the uterine stroma of ovariectomised rats have been studied over the 24 hours following an injection of progesterone. Autoradiographically, the rate of incorporation of [3H]lysine falls 1 hour after progesterone, rising progressively at 3 and 7 hours to levels higher than in control animals. A gradient of grain density is evident at 1, 3 and 7 hours, higher in regions adjacent to luminal epithelium than near the muscularis. No such gradient appears relative to glandular epithelium. Morphometric studies show that the array of stromal cells 24 hours after progesterone is similar to that in control rats, except that cells near the luminal epithelium are larger in the former group. At intermediate times, changes in cell size and spacing occur throughout the stroma in patterns that vary with distance from luminal epithelium. The organisation and activity of cells in the uterine stroma change in response to progesterone in a manner conditioned by their position in the uterus, in particular by their distance from luminal epithelium.

摘要

在给去卵巢大鼠注射孕酮后的24小时内,对其子宫基质中细胞的组织和活性进行了研究。通过放射自显影术发现,注射孕酮1小时后,[3H]赖氨酸的掺入率下降,在3小时和7小时逐渐上升至高于对照动物的水平。在1小时、3小时和7小时时,可见颗粒密度梯度,靠近腔上皮的区域比靠近肌层的区域更高。相对于腺上皮则未出现这种梯度。形态计量学研究表明,注射孕酮24小时后基质细胞的排列与对照大鼠相似,只是前一组中靠近腔上皮的细胞更大。在中间时间段,整个基质中细胞大小和间距的变化模式随距腔上皮的距离而变化。子宫基质中细胞的组织和活性会根据孕酮的作用而发生变化,其变化方式受细胞在子宫中的位置影响,特别是受其与腔上皮距离的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db8/1171847/11284ee3603b/janat00207-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db8/1171847/2ae46cc6b311/janat00207-0099-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db8/1171847/11284ee3603b/janat00207-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db8/1171847/2ae46cc6b311/janat00207-0099-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db8/1171847/11284ee3603b/janat00207-0106-a.jpg

相似文献

1
Cell organization in the stroma of the rat uterus. II. Responses to progesterone in the ovariectomised rat.大鼠子宫基质中的细胞组织。II. 去卵巢大鼠对孕酮的反应。
J Anat. 1983 Oct;137 (Pt 3)(Pt 3):541-53.
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本文引用的文献

1
Morphometric studies of the response of the luminal epithelium in the rat uterus to exogenous hormones.大鼠子宫腔上皮对外源激素反应的形态计量学研究。
J Anat. 1980 Jun;130(Pt 4):867-81.
2
Cell organization in the stroma of the rat uterus. I. The ovariectomised rat.大鼠子宫基质中的细胞组织。I. 去卵巢大鼠。
J Anat. 1982 Dec;135(Pt 4):707-18.
3
The distribution of ( 3 H)progesterone and ( 3 H)megestrol acetate in the uterus of the ovariectomized rat.(3H)孕酮和(3H)醋酸甲地孕酮在去卵巢大鼠子宫中的分布。
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Analysis of the effects of progesterone on the synthesis of RNA and protein in the uterus of the ovariectomized rat and on the development of an iodide concentrating mechanism.孕酮对去卵巢大鼠子宫中RNA和蛋白质合成以及碘浓缩机制发育的影响分析。
J Endocrinol. 1972 Jun;53(3):363-74. doi: 10.1677/joe.0.0530363.
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Cellular and subcellular localization of (3H)-progesterone and its metabolites in rat uterus studied by autoradiography.通过放射自显影术研究大鼠子宫中(3H)-孕酮及其代谢产物的细胞和亚细胞定位。
J Steroid Biochem. 1973 Sep;4(5):477-81. doi: 10.1016/0022-4731(73)90062-9.
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Uterine stromal morphology of the spayed virgin rat when prepared with progesterone and oestrogen for implantation.切除卵巢的未交配大鼠在使用孕酮和雌激素准备用于着床时的子宫基质形态。
Z Anat Entwicklungsgesch. 1973;141(2):161-9. doi: 10.1007/BF00519883.
7
Attachment reaction of rat uterine luminal epithelium. I. Gross and fine structure of the endometrium or the spayed, virgin rat.
Acta Soc Med Ups. 1971;76(3-4):91-109.
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Tranmission of signals in embryonic induction.胚胎诱导中的信号传递。
Med Biol. 1976 Apr;54(2):108-28.
9
Quantitative studies of the effect of progesterone on endometrial morphology of the spayed rat.孕酮对去卵巢大鼠子宫内膜形态学影响的定量研究。
Anat Embryol (Berl). 1975 Nov 6;148(1):47-58. doi: 10.1007/BF00315562.
10
Epithelial-stromal interactions in development of the urogenital tract.泌尿生殖道发育中的上皮-间质相互作用。
Int Rev Cytol. 1976;47:137-94. doi: 10.1016/s0074-7696(08)60088-1.