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CD68+ M1 巨噬细胞与胎儿生长受限的胎盘功能不全有关。

CD68+ M1 MACROPHAGES IS ASSOCIATED WITH PLACENTAL INSUFFICIENCY UNDER FETAL GROWTH RESTRICTION.

机构信息

UKRAINIAN MEDICAL STOMATOLOGICAL ACADEMY, POLTAVA, UKRAINE.

出版信息

Wiad Lek. 2021;74(2):213-219.

Abstract

OBJECTIVE

The aim: To elucidate the possible involvement of M1 and M2 macrophages in the placentas of women, whose pregnancies were complicated by fetal growth restriction (FGR) and resulted in term births after 37 weeks of gestation and preterm births up to 37 weeks of gestation.

PATIENTS AND METHODS

Materials and methods: CD68+ and CD163+ macrophages were studied by immunohistochemical method, placental morphology in the placentas of 16 women whose pregnancies were complicated by FGR and resulted in term births at a gestational age after 37 weeks (1-st group, n = 7) or resulted in preterm births at a gestational age up to 37 weeks (2-nd group, n = 9). The control group consisted of 10 placentas of women with physiological pregnancies and births.

RESULTS

Results: Women 2-nd group showed significantly low weight of the placenta, a short gestation period at the time of delivery, and a prolonged labor period than women of the control group (p <0.001; p <0.001; p <0.05, respectively). The level of CD68+ and CD163+ macrophages in the placentas of women 2-nd group was significantly higher than in woman 1-st group (p <0.001, p <0.001, respectively). A significant correlation was found between the expression level of CD68+ monocytes in the intervillous space and the weight of a newborn (r = - 0.765; p = 0.016) in women 2-nd group.

CONCLUSION

Conclusions: These studies suggest that in the placentas of women whose pregnancies were complicated by FGR and resulted in preterm births, the increased activation of CD68+ macrophages of the pro-inflammatory pool may be associated with disorders of the vascular and stromal component of the villous chorion with the development of involutive and dystrophic changes. In general, this fact probably determines the progress of chronic placental insufficiency and aggravates the development of fetal growth restriction.

摘要

目的

阐明 M1 和 M2 巨噬细胞在胎盘组织中的可能作用,这些胎盘来自于妊娠合并胎儿生长受限(FGR)并足月产(妊娠 37 周后)或早产(妊娠 37 周前)的女性。

患者与方法

使用免疫组织化学方法研究 CD68+和 CD163+巨噬细胞。16 名妊娠合并 FGR 且足月产(妊娠 37 周后)(第 1 组,n=7)或早产(妊娠 37 周前)(第 2 组,n=9)的女性胎盘组织中 CD68+和 CD163+巨噬细胞。对照组为 10 例生理妊娠和分娩的女性胎盘。

结果

第 2 组女性胎盘重量明显较低,分娩时的妊娠周期较短,分娩时间较长(p<0.001;p<0.001;p<0.05)。第 2 组女性胎盘 CD68+和 CD163+巨噬细胞的水平明显高于第 1 组(p<0.001;p<0.001)。第 2 组女性胎盘绒毛间质中 CD68+单核细胞的表达水平与新生儿体重呈显著负相关(r=-0.765;p=0.016)。

结论

这些研究表明,在妊娠合并 FGR 且早产的女性胎盘组织中,促炎池 CD68+巨噬细胞的过度激活可能与绒毛膜绒毛血管和基质成分的紊乱有关,进而导致退行性和营养不良性变化。总的来说,这一事实可能决定了慢性胎盘功能不全的进展,并加重了胎儿生长受限的发展。

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