Kwan M, Hazan A, Zhang J, Jones R L, Harris L K, Whittle W, Keating S, Dunk C E, Lye S J
Department of Physiology, Faculty of Medicine, University of Toronto, Toronto M5G 1E2, Canada; Research Centre for Women's and Infants Health, Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, Toronto M5T 3H7, Canada.
Department of Physiology, Faculty of Medicine, University of Toronto, Toronto M5G 1E2, Canada.
Placenta. 2014 Dec;35(12):1027-34. doi: 10.1016/j.placenta.2014.09.018. Epub 2014 Oct 6.
Decidual leukocytes are critical to the development of the fetomaternal interface, regulating tolerance to the semi-allogeneic fetus and vascular transformation of the uterine spiral arteries. Despite the continuation of these processes beyond the first trimester of pregnancy, the second trimester has largely been unstudied, with investigation focusing on early gestation and term tissues. We sought to characterize changes in decidual leukocyte populations from first to second trimester.
Multicolor flow cytometry was performed on isolated decidual leukocytes from elective terminations of pregnancy between 6 and 20 weeks of gestation for study of first (6-12 weeks) and second trimesters (13-20 weeks). Specific subpopulations were identified by comparison to isotype and fluorescent-minus-one (FMO) controls.
Decidual natural killer cells (CD56(+)CD16(-)CD3(-)) did not change in number, although a population of dNK with decreased CD56 brightness was observed in second trimester decidua. CD14(+)HLA-DR(+) macrophage numbers declined from first to second trimester (p = 0.031), yet a CD163(+)CD206(+) subset designating alternatively activated M2-like macrophages increased during the same period (p = 0.015). Intermediate CD205(+) dendritic cells demonstrated significant decline (p = 0.022), but immature CD209(+) and mature CD83(+) dendritic cells did not differ between trimesters. Total CD3(+) and CD3(+)CD4(+) T lymphocytes increased (p = 0.0079, p = 0.0028); CD3(+)CD8(+) T cells trended towards increase but did not differ significantly.
Several changes in leukocyte subsets are observed in the second trimester that promote a tolerogenic and angiogenic decidual microenvironment through mid-gestation.
蜕膜白细胞对于母胎界面的发育至关重要,可调节对半异体胎儿的耐受性以及子宫螺旋动脉的血管转化。尽管这些过程在妊娠早期之后仍在持续,但妊娠中期在很大程度上尚未得到研究,研究主要集中在妊娠早期和足月组织。我们试图描述从妊娠早期到中期蜕膜白细胞群体的变化。
对妊娠6至20周选择性终止妊娠时分离出的蜕膜白细胞进行多色流式细胞术,以研究妊娠早期(6至12周)和中期(13至20周)。通过与同型对照和荧光减一(FMO)对照比较来鉴定特定亚群。
蜕膜自然杀伤细胞(CD56(+)CD16(-)CD3(-))数量未发生变化,尽管在妊娠中期蜕膜中观察到一群CD56亮度降低的dNK细胞。从妊娠早期到中期,CD14(+)HLA-DR(+)巨噬细胞数量下降(p = 0.031),然而,在此期间指定为交替激活的M2样巨噬细胞的CD163(+)CD206(+)亚群增加(p = 0.015)。中间型CD205(+)树突状细胞显著减少(p = 0.022),但未成熟的CD209(+)和成熟的CD83(+)树突状细胞在不同孕期之间没有差异。总CD3(+)和CD3(+)CD4(+) T淋巴细胞增加(p = 0.0079,p = 0.0028);CD3(+)CD8(+) T细胞有增加趋势,但差异不显著。
在妊娠中期观察到白细胞亚群的一些变化,这些变化在妊娠中期促进了具有耐受性和血管生成性的蜕膜微环境。