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月经来源干细胞对小鼠卵巢早衰修复作用的研究

Study of the reparative effects of menstrual-derived stem cells on premature ovarian failure in mice.

作者信息

Wang Zhen, Wang Yueling, Yang Ting, Li Jing, Yang Xinyuan

机构信息

Department of Gynecology and Obstetrics, First Affiliated Hospital, Xi'an Jiaotong University, Xi'an, 710061, People's Republic of China.

Center for Translational Medicine, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, People's Republic of China.

出版信息

Stem Cell Res Ther. 2017 Jan 23;8(1):11. doi: 10.1186/s13287-016-0458-1.

Abstract

BACKGROUND

Young female patients who receive chemotherapy frequently face premature ovarian failure (POF). The therapeutic potential of stem cells in these patients has been explored in stem cells derived from different sources. However, many of these types of stem cells are either difficult to obtain or obtaining them involves invasive procedures. Here, we show that menstrual-derived stem cells (MenSCs) are easy to access and exhibit mesenchymal stem cell-like properties. MenSCs are therefore a novel source of stem cells that can be used for tissue repair. The aim of this study was to explore the reparative capacity and the mechanism underlying the activities of MenSCs.

METHODS

POF mouse models were established by 7 consecutive days of intraperitoneal injection of cisplatin, and then MenSCs or MenSC-derived conditioned media (CM) were infused via the tail vein. The ovaries were excised after either 7 or 21 days of treatment and the follicles were counted and categorized. Apoptosis of granulosa cells was observed by terminal deoxynucleotidyl transferase mediated dUTP nick end labelling staining. Ovarian function was evaluated by monitoring serum sex hormone levels. Furthermore, MenSC tracking, Q-PCR, and small interfering RNA transfection were used to reveal the inner mechanism of repair.

RESULTS

MenSC transplantation could improve the ovarian microenvironment by reducing apoptosis in granulosa cells and the fibrosis of ovarian interstitium, which contributes to increase the follicular numbers and return sex hormone levels to normal values. Meanwhile, the transplanted MenSCs directively migrate to ovarian interstitium to play a role in repair rather than differentiate to oocytes directly. Additionally, MenSCs and CM derived from these cells exerted protective effects on damaged ovaries partially by secreting FGF2.

CONCLUSION

MenSCs repair ovarian injury, improve ovarian function, and stimulate regeneration, suggesting that transplantation of MenSCs may provide an effective and novel method for treating POF.

摘要

背景

接受化疗的年轻女性患者经常面临卵巢早衰(POF)。已经在源自不同来源的干细胞中探索了这些患者中干细胞的治疗潜力。然而,这些类型的干细胞中的许多要么难以获得,要么获取它们涉及侵入性操作。在这里,我们表明月经来源的干细胞(MenSCs)易于获取并表现出间充质干细胞样特性。因此,MenSCs是一种可用于组织修复的新型干细胞来源。本研究的目的是探索MenSCs的修复能力及其活动背后的机制。

方法

通过连续7天腹腔注射顺铂建立POF小鼠模型,然后通过尾静脉注入MenSCs或MenSC来源的条件培养基(CM)。在治疗7天或21天后切除卵巢,对卵泡进行计数和分类。通过末端脱氧核苷酸转移酶介导的dUTP缺口末端标记染色观察颗粒细胞的凋亡。通过监测血清性激素水平评估卵巢功能。此外,使用MenSC追踪、Q-PCR和小干扰RNA转染来揭示修复的内在机制。

结果

MenSC移植可通过减少颗粒细胞凋亡和卵巢间质纤维化来改善卵巢微环境,这有助于增加卵泡数量并使性激素水平恢复正常。同时,移植的MenSCs定向迁移到卵巢间质中发挥修复作用,而不是直接分化为卵母细胞。此外,MenSCs和源自这些细胞的CM通过分泌FGF2对受损卵巢发挥部分保护作用。

结论

MenSCs修复卵巢损伤,改善卵巢功能并刺激再生,表明MenSCs移植可能为治疗POF提供一种有效且新颖的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4847/5259841/d4bd987275fb/13287_2016_458_Fig1_HTML.jpg

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