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敲低长链非编码 RNA H19 可抑制体内子宫内膜异位症。

Knockdown of lncRNA H19 suppresses endometriosis in vivo.

机构信息

Department of Obstetrics and Gynecology, Jinshan Hospital of Fudan University, Shanghai, China.

Department of Gynecology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.

出版信息

Braz J Med Biol Res. 2021 Feb 26;54(4):e10117. doi: 10.1590/1414-431X202010117. eCollection 2021.

DOI:10.1590/1414-431X202010117
PMID:33656053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7917710/
Abstract

The long noncoding RNA (lncRNA) H19 is involved in the pathogenesis of endometriosis by modulating the proliferation and invasion of ectopic endometrial cells in vitro, but related in vivo studies are rare. This study aimed to investigate the role of lncRNA H19 in a nude mouse model of endometriosis. Ectopic endometrial stromal cells (ecESCs) were isolated from ectopic endometrium of patients with endometriosis and infected with lentiviruses expressing short hairpin RNA (shRNA) negative control (LV-NC-shRNA) or lncRNA-H19 shRNA (LV-H19-shRNA). The ecESCs infected with LV-NC-shRNA and LV-H19-shRNA were subcutaneously implanted into forty 6- to 8-week-old female nude mice. The size and weight of the endometriotic implants were measured at 1, 2, 3, and 4 weeks after implantation and compared, and lncRNA H19 levels in endometriotic implants were evaluated using real-time polymerase chain reaction (RT-PCR). All nude mice survived the experimental period, and no significant differences in body weight were observed between the experimental group and the control group. All nude mice developed histologically confirmed subcutaneous endometriotic lesions with glandular structures and stroma after 1 week of implantation. The subcutaneous lesions in the LV-NC-shRNA group after 1, 2, 3, and 4 weeks of implantation were larger than those in the LV-H19-shRNA group, and lncRNA H19 levels in subcutaneous lesions in the LV-NC-shRNA group were significantly higher than those in the LV-H19-shRNA group. Knockdown of lncRNA H19 suppresses endometriosis in vivo. Further study is required to explore the underlying mechanism in the future.

摘要

长链非编码 RNA(lncRNA)H19 通过调节体外异位子宫内膜细胞的增殖和侵袭参与子宫内膜异位症的发病机制,但相关的体内研究很少。本研究旨在探讨 lncRNA H19 在子宫内膜异位症裸鼠模型中的作用。从子宫内膜异位症患者的异位子宫内膜中分离出异位子宫内膜基质细胞(ecESCs),并用表达短发夹 RNA(shRNA)阴性对照(LV-NC-shRNA)或 lncRNA-H19 shRNA(LV-H19-shRNA)的慢病毒感染。将感染了 LV-NC-shRNA 和 LV-H19-shRNA 的 ecESCs 皮下植入 40 只 6-8 周龄的雌性裸鼠。在植入后 1、2、3 和 4 周测量子宫内膜异位症植入物的大小和重量,并使用实时聚合酶链反应(RT-PCR)评估子宫内膜异位症植入物中的 lncRNA H19 水平。所有裸鼠均在实验期间存活,实验组和对照组之间的体重无显著差异。所有裸鼠在植入后 1 周均形成具有腺体结构和基质的皮下子宫内膜异位症病变,组织学证实。在植入后 1、2、3 和 4 周,LV-NC-shRNA 组的皮下病变大于 LV-H19-shRNA 组,并且 LV-NC-shRNA 组的皮下病变中的 lncRNA H19 水平明显高于 LV-H19-shRNA 组。敲低 lncRNA H19 抑制体内子宫内膜异位症。未来需要进一步研究探索其潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/2218e6424c0e/1414-431X-bjmbr-54-4-e10117-gf004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/473b827fd28e/1414-431X-bjmbr-54-4-e10117-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/e42fd742c40a/1414-431X-bjmbr-54-4-e10117-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/35bee0cf5cdc/1414-431X-bjmbr-54-4-e10117-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/2218e6424c0e/1414-431X-bjmbr-54-4-e10117-gf004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/473b827fd28e/1414-431X-bjmbr-54-4-e10117-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/e42fd742c40a/1414-431X-bjmbr-54-4-e10117-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/35bee0cf5cdc/1414-431X-bjmbr-54-4-e10117-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48a6/7917710/2218e6424c0e/1414-431X-bjmbr-54-4-e10117-gf004.jpg

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本文引用的文献

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Progesterone and Estrogen Signaling in the Endometrium: What Goes Wrong in Endometriosis?子宫内膜中孕激素和雌激素信号转导:子宫内膜异位症中哪里出了问题?
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