• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

一种新型的早期子宫内膜异位症病变体外模型表明,子宫内膜细胞与间皮细胞的附着取决于子宫内膜细胞的来源。

A novel in vitro model of the early endometriotic lesion demonstrates that attachment of endometrial cells to mesothelial cells is dependent on the source of endometrial cells.

作者信息

Lucidi R Scott, Witz Craig A, Chrisco Michelle, Binkley Peter A, Shain Sydney A, Schenken Robert S

机构信息

Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Texas Health Science Center, San Antonio, Texas 78284, USA.

出版信息

Fertil Steril. 2005 Jul;84(1):16-21. doi: 10.1016/j.fertnstert.2004.10.058.

DOI:10.1016/j.fertnstert.2004.10.058
PMID:16009148
Abstract

OBJECTIVE

To characterize the source of variability in endometrial stromal cell (ESC) binding to peritoneal mesothelial cells (PMC).

DESIGN

In vitro study.

SETTING

University medical center.

PATIENT(S): Reproductive-age women without endometriosis undergoing surgery for benign conditions.

INTERVENTION(S): None.

MAIN OUTCOME MEASURE(S): Binding of ESCs (n = 9) to PMCs collected from the anterior abdominal wall (AAW) (n = 5), a commercially available mesothelial cell line (LP9) (three different passages) and normal ovarian surface epithelium (NOSE) (n = 5).

RESULT(S): There were no differences in the binding of same-source ESCs to mesothelial cells obtained from the AAW of different women, to different passages of LP9s or to NOSE of different women. There was a trend toward increased binding of ESCs to NOSE compared to AAW PMCs. In contrast, there were significant differences in the ability of ESCs obtained from different women to bind to same-source PMCs.

CONCLUSION(S): There is significant variability in ESC binding to PMCs. This variation is dependent primarily on the source of the ESCs. The ESC binding to LP9 PMCs was similar to AAW PMCs and NOSE.

摘要

目的

明确子宫内膜间质细胞(ESC)与腹膜间皮细胞(PMC)结合的变异来源。

设计

体外研究。

地点

大学医学中心。

患者

因良性疾病接受手术的无子宫内膜异位症的育龄妇女。

干预措施

无。

主要观察指标

9个ESC与从前腹壁(AAW)采集的5个PMC、一种市售间皮细胞系(LP9)(三种不同传代)以及5个正常卵巢表面上皮(NOSE)的结合情况。

结果

同源ESC与从不同女性的AAW获取的间皮细胞、不同传代的LP9或不同女性的NOSE的结合无差异。与AAW PMC相比,ESC与NOSE的结合有增加趋势。相反,不同女性来源的ESC与同源PMC结合的能力存在显著差异。

结论

ESC与PMC的结合存在显著变异。这种变异主要取决于ESC的来源。ESC与LP9 PMC的结合类似于与AAW PMC和NOSE的结合。

相似文献

1
A novel in vitro model of the early endometriotic lesion demonstrates that attachment of endometrial cells to mesothelial cells is dependent on the source of endometrial cells.一种新型的早期子宫内膜异位症病变体外模型表明,子宫内膜细胞与间皮细胞的附着取决于子宫内膜细胞的来源。
Fertil Steril. 2005 Jul;84(1):16-21. doi: 10.1016/j.fertnstert.2004.10.058.
2
Possible involvement of signal transducer and activator of transcription-3 in cell-cell interactions of peritoneal macrophages and endometrial stromal cells in human endometriosis.信号转导子和转录激活子 3 可能参与人子宫内膜异位症中腹腔巨噬细胞和子宫内膜基质细胞的细胞间相互作用。
Fertil Steril. 2013 May;99(6):1705-13. doi: 10.1016/j.fertnstert.2013.01.133. Epub 2013 Feb 22.
3
Decreased suppression of interleukin-6 after treatment with medroxyprogesterone acetate and danazol in endometrial stromal cells of women with adenomyosis.在患有子宫腺肌病的女性子宫内膜基质细胞中,醋酸甲羟孕酮和达那唑治疗后白细胞介素-6的抑制作用降低。
Fertil Steril. 2006 Nov;86(5):1459-65. doi: 10.1016/j.fertnstert.2006.04.034. Epub 2006 Sep 20.
4
Modeling the early endometriotic lesion: mesothelium-endometrial cell co-culture increases endometrial invasion and alters mesothelial and endometrial gene transcription.早期子宫内膜异位症病变建模:间皮细胞与子宫内膜细胞共培养可增加子宫内膜侵袭并改变间皮细胞和子宫内膜的基因转录。
Fertil Steril. 2008 Oct;90(4 Suppl):1487-95. doi: 10.1016/j.fertnstert.2007.09.047. Epub 2007 Dec 27.
5
Menstrual endometrial cells from women with endometriosis demonstrate increased adherence to peritoneal cells and increased expression of CD44 splice variants.子宫内膜异位症患者的月经子宫内膜细胞表现出对腹膜细胞的黏附增加和 CD44 剪接变异体表达增加。
Fertil Steril. 2010 Apr;93(6):1745-9. doi: 10.1016/j.fertnstert.2008.12.012. Epub 2009 Feb 6.
6
NME1 suppression promotes growth, adhesion and implantation of endometrial stromal cells via Akt and MAPK/Erk1/2 signal pathways in the endometriotic milieu.NME1 抑制通过 Akt 和 MAPK/Erk1/2 信号通路促进子宫内膜基质细胞在子宫内膜异位症微环境中的生长、黏附和着床。
Hum Reprod. 2013 Oct;28(10):2822-31. doi: 10.1093/humrep/det248. Epub 2013 Jul 14.
7
Basal release of urokinase plasminogen activator, plasminogen activator inhibitor-1, and soluble plasminogen activator receptor from separated and cultured endometriotic and endometrial stromal and epithelial cells.从分离培养的子宫内膜异位症、子宫内膜基质和上皮细胞中尿激酶型纤溶酶原激活物、纤溶酶原激活物抑制剂-1和可溶性纤溶酶原激活物受体的基础释放。
Fertil Steril. 2005 Apr;83 Suppl 1:1155-60. doi: 10.1016/j.fertnstert.2004.09.033.
8
Estrogen receptor beta and matrix metalloproteinase 1 are coexpressed in uterine endometrium and endometriotic lesions of patients with endometriosis.雌激素受体β和基质金属蛋白酶1在子宫内膜异位症患者的子宫内膜及异位内膜病灶中共同表达。
Fertil Steril. 2005 Oct;84 Suppl 2:1249-56. doi: 10.1016/j.fertnstert.2005.06.014.
9
Induction of monocyte chemotactic protein-1 in peritoneal mesothelial and endometrial cells by oxidized low-density lipoprotein and peritoneal fluid from women with endometriosis.氧化型低密度脂蛋白和子宫内膜异位症患者的腹腔液诱导腹膜间皮细胞和子宫内膜细胞产生单核细胞趋化蛋白-1
Fertil Steril. 2002 Oct;78(4):843-8. doi: 10.1016/s0015-0282(02)03333-2.
10
Effect of monocyte chemoattractant protein-1 and estradiol on the secretion of vascular endothelial growth factor in endometrial stromal cells in vitro.单核细胞趋化蛋白-1和雌二醇对体外培养的子宫内膜基质细胞中血管内皮生长因子分泌的影响。
Fertil Steril. 2005 Dec;84(6):1793-6. doi: 10.1016/j.fertnstert.2005.03.090.

引用本文的文献

1
Role of Transcription Factor, LIM Homeobox 9 (LHX9) in Inflammatory Response by PGE2 and Thrombin in SERPINA1-Silencing Endometrial Stromal Cells.转录因子LIM同源框9(LHX9)在丝氨酸蛋白酶抑制剂A1(SERPINA1)沉默的子宫内膜基质细胞中由前列腺素E2(PGE2)和凝血酶介导的炎症反应中的作用
Mol Reprod Dev. 2025 Aug;92(8):e70046. doi: 10.1002/mrd.70046.
2
Leveraging epigenetic aberrations in the pathogenesis of endometriosis: from DNA methylation to non-coding RNAs.利用表观遗传异常在子宫内膜异位症发病机制中的作用:从DNA甲基化到非编码RNA
Front Genet. 2025 Jul 28;16:1597287. doi: 10.3389/fgene.2025.1597287. eCollection 2025.
3
Hypersensitive intercellular responses of endometrial stromal cells drive invasion in endometriosis.
子宫内膜间质细胞的超敏细胞间反应驱动子宫内膜异位症的侵袭。
Elife. 2024 Dec 11;13:e94778. doi: 10.7554/eLife.94778.
4
A seed or soil problem in early endometriosis: stromal cell origin drives cellular invasion and coupling over mesothelial cell origin.早期子宫内膜异位症中的种子或土壤问题:基质细胞起源驱动细胞侵袭和与间皮细胞起源的偶联,而不是间皮细胞起源。
F S Sci. 2024 Nov;5(4):395-403. doi: 10.1016/j.xfss.2024.08.001. Epub 2024 Aug 8.
5
Long-Term Maintenance of Viable Human Endometrial Epithelial Cells to Analyze Estrogen and Progestin Effects.长期维持有活力的人子宫内膜上皮细胞以分析雌激素和孕激素的作用。
Cells. 2024 May 9;13(10):811. doi: 10.3390/cells13100811.
6
A Systematic Review of Systematic Reviews on the Use of Aromatase Inhibitors for the Treatment of Endometriosis: The Evidence to Date.一篇关于芳香化酶抑制剂治疗子宫内膜异位症的系统评价的系统评价:迄今为止的证据。
Drug Des Devel Ther. 2023 May 4;17:1329-1346. doi: 10.2147/DDDT.S315726. eCollection 2023.
7
Intrinsic unilateral ureteral endometriosis: A rare case report.原发性单侧输尿管子宫内膜异位症:一例罕见病例报告
Int J Surg Case Rep. 2023 Mar;104:107966. doi: 10.1016/j.ijscr.2023.107966. Epub 2023 Mar 4.
8
Toll-like receptor signaling pathway triggered by inhibition of serpin A1 stimulates production of inflammatory cytokines by endometrial stromal cells.丝氨酸蛋白酶抑制剂 A1 抑制物激活 toll 样受体信号通路诱导子宫内膜基质细胞分泌炎性细胞因子。
Front Endocrinol (Lausanne). 2022 Aug 24;13:966455. doi: 10.3389/fendo.2022.966455. eCollection 2022.
9
Epigenetic Factors in Eutopic Endometrium in Women with Endometriosis and Infertility.子宫内膜异位症和不孕症女性在位内膜中的表观遗传因素
Int J Mol Sci. 2022 Mar 30;23(7):3804. doi: 10.3390/ijms23073804.
10
Cellular junction and mesenchymal factors delineate an endometriosis-specific response of endometrial stromal cells to the mesothelium.细胞连接和间质因子描绘了子宫内膜基质细胞对间皮的子宫内膜异位症特异性反应。
Mol Cell Endocrinol. 2022 Jan 1;539:111481. doi: 10.1016/j.mce.2021.111481. Epub 2021 Oct 6.