Suppr超能文献

通过原位杂交技术对人子宫内膜中补体成分3的表达进行定位。

Localization of the expression of complement component 3 in the human endometrium by in situ hybridization.

作者信息

Sayegh R A, Tao X J, Awwad J T, Isaacson K B

机构信息

Vincent Memorial Obstetrics and Gynecology Service, Massachusetts General Hospital, Boston, USA.

出版信息

J Clin Endocrinol Metab. 1996 Apr;81(4):1641-9. doi: 10.1210/jcem.81.4.8636381.

Abstract

C3 production by the human endometrium has been previously described. The objective of the current study was to localize the site of expression and regulation of the third component of complement, C3, in the endometrium. Eight secretory and eight proliferative archival endometrial samples from hysterectomy and endometrial biopsy specimens were used for in situ hybridization analysis. This analysis was performed with a radiolabeled riboprobe synthesized from a 736-bp template representing sequence 1944-2680 of the human C3 complementary DNA. Duplicate sections were hybridized with sense and antisense riboprobes. Resultant autoradiograms were analyzed qualitatively by light- and darkfield microscopy. In proliferative endometrium, minimal expression of C3 was observed and was limited to a few stromal patches and glands throughout the section. In the secretory samples, prominent C3 expression was observed in both the glands and stroma of the basalis layer. Endometrial lymphocytes did not express C3. Endometrial stromal and glandular cells express the C3 gene. Endometrial lymphocytes did not express C3, but other nondistinct lymphoid elements scattered in the stroma may be expressing C3. There was a visibly more intense expression of C3 in the basalis layer of the secretory endometrium than in proliferative endometrium. The spatial and temporal pattern of C3 expression may have implications in normal menstrual physiology and in the immunological response of the endometrium to the invading trophoblast during placentation.

摘要

此前已有关于人子宫内膜产生补体C3的描述。本研究的目的是确定补体第三成分C3在子宫内膜中的表达部位及其调控机制。从子宫切除标本和子宫内膜活检标本中选取8份分泌期和8份增殖期的存档子宫内膜样本,用于原位杂交分析。该分析使用了由一个736 bp模板合成的放射性标记核糖探针,该模板代表人类C3互补DNA序列1944 - 2680。将复制的切片分别与正义和反义核糖探针杂交。通过明场和暗场显微镜对所得放射自显影片进行定性分析。在增殖期子宫内膜中,观察到C3的表达极少,且仅限于整个切片中的少数基质斑和腺体。在分泌期样本中,基底层的腺体和基质中均观察到明显的C3表达。子宫内膜淋巴细胞不表达C3。子宫内膜基质细胞和腺细胞表达C3基因。子宫内膜淋巴细胞不表达C3,但散在基质中的其他未明确的淋巴样成分可能表达C3。分泌期子宫内膜基底层的C3表达明显比增殖期子宫内膜更强。C3表达的时空模式可能对正常月经生理以及胎盘形成过程中子宫内膜对侵入的滋养层的免疫反应具有影响。

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