Uterine administration of C-X-C motif chemokine ligand 12 increases the pregnancy rates in mice with induced endometriosis

Ana Carolina Japur de Sá Rosa-e-Silva M.D. , Ramanaiah Mamillapalli Ph.D. , Julio Cesar Rosa-e-Silva M.D. , Abdullah Ucar M.D. , Joshua Schwartz B.A. , Hugh S. Taylor M.D.
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Abstract

Objective

To study the effect of intrauterine injection of C-X-C motif chemokine ligand 12 (CXCL12), also known as a stem cell chemoattractant (stromal cell-derived factor 1), on fertility and endometrial receptivity in mice with endometriosis.

Design

Laboratory study.

Setting

Academic Medical Center.

Animal(s)

Fifty-six mice underwent chemotherapy and bone marrow transplantation. Thirty-six of these mice underwent either surgery to induce endometriosis (n = 20) or sham surgery (n = 16).

Intervention(s)

Injection of CXCL12 as a potential therapeutic agent to improve fertility in endometriosis.

Main Outcome Measure(s)

Pregnancy rate, bone marrow–derived cell (BMDC) recruitment and endometrial receptivity markers.

Result(s)

The mice with or without endometriosis received a single uterine injection of either CXCL12 or placebo. Uterine injection of CXCL12 increased the pregnancy rates in a mouse model of endometriosis. Mice were euthanized after delivery, and implantation markers homeobox A11, alpha-v beta-3 integrin, and progesterone receptor were analyzed by immunohistochemistry, whereas green fluorescent protein positive BMDC recruitment was quantified by immunohistochemistry and immunofluorescence. The sham surgery groups without endometriosis had the highest cumulative pregnancy rate (100%) regardless of CXCL12 treatment. The endometriosis group treated with placebo had the lowest pregnancy rate. An increased pregnancy rate was noted in the endometriosis group after treatment with CXCL12. There was also an increase in BMDC recruitment and endometrial expression of progesterone receptor and alpha-v beta-3 integrin in the endometriosis group that received CXCL12 compared with that in the endometriosis group that received placebo.

Conclusion(s)

Uterine injection of CXCL12 increased the pregnancy rates in a mouse model of endometriosis. These results suggest that CXCL12 has a potential role as a therapeutic agent in women with infertility related to endometriosis and potentially other endometrial receptivity defects.

子宫给予C-X-C基序趋化因子配体12可增加诱导子宫内膜异位症小鼠的妊娠率
目的研究子宫内注射C-X-C基序趋化因子配体12 (CXCL12)对子宫内膜异位症小鼠生育能力和子宫内膜容受性的影响,CXCL12也被称为干细胞趋化因子1。DesignLaboratory研究。56只小鼠接受了化疗和骨髓移植。其中36只小鼠接受了手术诱导子宫内膜异位症(n = 20)或假手术(n = 16)。干预措施(s)注射CXCL12作为一种潜在的治疗药物来提高子宫内膜异位症的生育能力。主要观察指标:妊娠率、骨髓源性细胞(BMDC)募集和子宫内膜容受性标志物。结果:有或没有子宫内膜异位症的小鼠接受单次子宫注射CXCL12或安慰剂。子宫注射CXCL12可提高子宫内膜异位症小鼠模型的妊娠率。分娩后对小鼠实施安乐死,免疫组化分析植入标记物同源盒A11、α -v β -3整合素和孕酮受体,免疫组化和免疫荧光定量测定绿色荧光蛋白阳性BMDC募集。无论CXCL12治疗与否,无子宫内膜异位症的假手术组累积妊娠率最高(100%)。子宫内膜异位症组接受安慰剂治疗的怀孕率最低。使用CXCL12治疗后,子宫内膜异位症组妊娠率增加。子宫内膜异位症组与安慰剂组相比,子宫内膜异位症组BMDC募集增加,子宫内膜孕酮受体和α -v β -3整合素表达增加。结论子宫内注射CXCL12可提高子宫内膜异位症小鼠的妊娠率。这些结果表明,CXCL12在子宫内膜异位症和其他子宫内膜容受性缺陷相关的不孕妇女中具有潜在的治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
F&S science
F&S science Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Urology
CiteScore
2.00
自引率
0.00%
发文量
0
审稿时长
51 days
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