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骨髓间充质干细胞修复环磷酰胺诱导的小鼠卵巢功能不全模型

Bone marrow mesenchymal stem cell repair of cyclophosphamide-induced ovarian insufficiency in a mouse model.

作者信息

Badawy Ahmed, Sobh Mohamed A, Ahdy Mohamed, Abdelhafez Mohamed Sayed

机构信息

Department of Obstetrics and Gynecology.

Department of Internal Medicine.

出版信息

Int J Womens Health. 2017 Jun 15;9:441-447. doi: 10.2147/IJWH.S134074. eCollection 2017.

DOI:10.2147/IJWH.S134074
PMID:28670143
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5479293/
Abstract

OBJECTIVE

Attempting in vivo healing of cyclophosphamide-induced ovarian insufficiency in a mouse model using bone marrow mesenchymal stem cells (BMMSCs).

METHODS

Female BALB/c white mice were used to prepare a model for premature ovarian failure by single intraperitoneal injection of cyclophosphamide (80 mg/kg). Ten mice were injected with BMMSCs and then sacrificed after 21 days for morphometric evaluation of the ovaries. Hormonal profile was evaluated while mice were being sacrificed. Another 10 mice were left for natural breeding with male mice, and 5 of these were injected with BMMSCs. Oocyte-like structures were obtained from 3 mice and were subjected to in vitro fertilization/intracytoplasmic sperm injection.

RESULTS

Morphometric analysis of the ovaries demonstrated the presence of newly formed primordial follicles. Contribution of MSCs to the formation of these follicles was proven by a labeling technique. There was a drop in estradiol and rise in follicle-stimulating hormone levels, followed by resumption of the hormonal levels to near normal 21 days after MSCs therapy. The 5 mice that were injected with MSCs became pregnant after natural breeding. Fertilization and further division was reported in 5 oocytes subjected to intracytoplasmic sperm injection, but division did not continue.

CONCLUSION

From this proof-of-concept trial, we can say that healing of damaged ovaries after chemotherapy in mice is possible using in vivo therapy with BMMSCs. This should open the gate for a series of animal studies that test the possibility of in vitro maturation of germinal epithelium of the ovary into mature oocytes.

摘要

目的

尝试在小鼠模型中使用骨髓间充质干细胞(BMMSCs)对环磷酰胺诱导的卵巢功能不全进行体内修复。

方法

雌性BALB/c白色小鼠通过单次腹腔注射环磷酰胺(80mg/kg)制备卵巢早衰模型。10只小鼠注射BMMSCs,21天后处死进行卵巢形态计量学评估。处死小鼠时评估激素水平。另外10只小鼠留作与雄性小鼠自然交配,其中5只注射BMMSCs。从3只小鼠获取类卵母细胞结构并进行体外受精/卵胞浆内单精子注射。

结果

卵巢形态计量学分析显示有新形成的原始卵泡。通过标记技术证实了间充质干细胞对这些卵泡形成的贡献。间充质干细胞治疗后21天,雌二醇水平下降,卵泡刺激素水平上升,随后激素水平恢复至接近正常。5只注射间充质干细胞的小鼠自然交配后怀孕。5个接受卵胞浆内单精子注射的卵母细胞有受精及进一步分裂的报道,但分裂未持续。

结论

从这个概念验证试验可以看出,在小鼠中使用BMMSCs进行体内治疗有可能修复化疗后受损的卵巢。这应该为一系列动物研究打开大门,这些研究将测试卵巢生发上皮体外成熟为成熟卵母细胞的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b3e/5479293/4f204deabf86/ijwh-9-441Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b3e/5479293/1a75319bc8cf/ijwh-9-441Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b3e/5479293/4f204deabf86/ijwh-9-441Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b3e/5479293/1a75319bc8cf/ijwh-9-441Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b3e/5479293/4f204deabf86/ijwh-9-441Fig5.jpg

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