与子痫前期相比,正常妊娠中内皮祖细胞亚群的变化。

Changes in endothelial progenitor cell subsets in normal pregnancy compared with preeclampsia.

作者信息

Parsanezhad Mohammad-Ebrahim, Attar Armin, Namavar-Jahromi Bahia, Khoshkhou Sara, Khosravi-Maharlooei Mohsen, Monabati Ahmad, Habibagahi Mojtaba

机构信息

Department of OB-GYN, Division of Infertility and Reproductive Medicine, Shiraz University of Medical Sciences, Shiraz, Iran; Infertility and Reproductive Medicine Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran; Cell and Molecular Medicine Research Club, Shiraz University of Medical Sciences, Shiraz, Iran; Department of Cardiovascular Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

J Chin Med Assoc. 2015 Jun;78(6):345-52. doi: 10.1016/j.jcma.2015.03.013. Epub 2015 May 23.

Abstract

BACKGROUND

The results of studies measuring the number of endothelial progenitor cells (EPCs) in normal pregnancies and in preeclampsia have been highly controversial or even contradictory because of cross-sectional designs and different methodologies enumerating three distinct subsets of EPCs: circulating angiogenic cells (CAC), colony-forming unit endothelial cell (CFU-ECs), and endothelial colony forming cells (ECFCs). To provide a clear explanation for these underlying controversies, we designed a prospective study to compare the number of all EPC subsets between three trimesters of normal gestation and a case-control study to compare these values as preeclampsia occurs with those from gestational age (GA) matched normal pregnancy.

METHODS

Samples from peripheral blood of nine women were taken during their three consecutive trimesters of normal pregnancy, and from eight women with preeclampsia. To cover most of the reported phenotypes for CACs and ECFCs in the literature, we enumerated 13 cell populations by quantitative flow cytometry using various combinations of the markers CD34, CD133, CD309, and CD45. We used routine culturing techniques to enumerate CFU-ECs.

RESULTS

The numbers of CACs and ECFCs were higher in women with preeclampsia (p = 0.014). By contrast, preeclampsia was associated with a reduced number of CFU-ECs (p = 0.039). The CAC number rose with the increase in GA (p = 0.016) during normal pregnancy, while the number of CFU-ECs and ECFCs did not differ during the trimesters.

CONCLUSION

Although we did demonstrate an increase in absolute counts of CACs and ECFCs in preeclampsia, fewer colony formation capacities indicated a loss in their functional capabilities. By contrast, the number of CACs increased without alterations in colony formation ability in normal pregnancy with the growth of the fetus. Here, by comparing different methodologies to calculate the number of EPC subsets, we could imitate the existing controversy in the literature for such calculations, which may help to elucidate clearer explanations.

摘要

背景

由于采用横断面设计以及枚举内皮祖细胞(EPC)三个不同亚群(循环血管生成细胞(CAC)、集落形成单位内皮细胞(CFU-EC)和内皮集落形成细胞(ECFC))的方法不同,测量正常妊娠和子痫前期中EPC数量的研究结果一直存在高度争议甚至相互矛盾。为了对这些潜在争议给出清晰解释,我们设计了一项前瞻性研究来比较正常妊娠三个孕期中所有EPC亚群的数量,并设计了一项病例对照研究,以比较子痫前期发生时这些数值与孕周(GA)匹配的正常妊娠的数值。

方法

采集9名正常妊娠女性连续三个孕期的外周血样本,以及8名单纯性高血压女性的外周血样本。为涵盖文献中报道的大多数CAC和ECFC表型,我们使用标记物CD34、CD133、CD309和CD45的各种组合,通过定量流式细胞术枚举13种细胞群。我们使用常规培养技术枚举CFU-EC。

结果

子痫前期女性的CAC和ECFC数量更高(p = 0.014)。相比之下,子痫前期与CFU-EC数量减少有关(p = 0.039)。正常妊娠期间,CAC数量随孕周增加而上升(p = 0.016),而CFU-EC和ECFC数量在各孕期无差异。

结论

尽管我们确实证明了子痫前期中CAC和ECFC的绝对计数增加,但集落形成能力降低表明其功能能力丧失。相比之下,正常妊娠时随着胎儿生长,CAC数量增加但集落形成能力无改变。在此,通过比较计算EPC亚群数量的不同方法,我们可以模拟文献中此类计算存在的争议,这可能有助于阐明更清晰的解释。

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