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发育中的人类胎盘中的Fcγ受体活性

Fc gamma-receptor activity in the developing human placenta.

作者信息

Jensen T S, Matre R

机构信息

Broegelmann Research Laboratory for Microbiology, University of Bergen, Norway.

出版信息

APMIS. 1995 Jun;103(6):433-8.

PMID:7546646
Abstract

The expression of Fc gamma receptors (Fc gamma R) and annexin II in 20 placentae (range 8-27 weeks' gestation) and in 3 full-term placentae was studied using monoclonal antibodies (mAbs) and soluble immune complexes. Functionally active Fc gamma R was detected on the trophoblast, endothelial cells, and stromal cells (Hofbauer cells) from the 8th week of gestation. Fc gamma RI (mAb 32.2) and Fc gamma RIII (mAb 3G8) were detected only on Hofbauer cells, whereas Fc gamma RII (IV3 and C1KM5) were detected both on Hofbauer cells and endothelial cells. Fc gamma RIII (anti-Leu-11b) and the IgG-binding molecule annexin II (mAb B1D6) were expressed by Hofbauer cells, endothelial cells, and the trophoblast. There was some variation in staining among the different specimens, but the number of positive cells as well as the staining intensity increased from the first to the second trimester. In first trimester placenta, staining was localized both to the syncytio- and cytotrophoblast, with the strongest intensity in the cytotrophoblast and at the boundary between the two cell layers. In second and third trimester placenta, staining was localized to the syncytiotrophoblast. The localization and distribution of Fc gamma R on the trophoblast during ontogeny is of interest with regard to its presumed role in the transport of IgG from mother to fetus.

摘要

利用单克隆抗体(mAb)和可溶性免疫复合物,研究了20例胎盘(妊娠8 - 27周)和3例足月胎盘组织中Fcγ受体(FcγR)和膜联蛋白II的表达情况。从妊娠第8周起,在滋养层细胞、内皮细胞和基质细胞(霍夫鲍尔细胞)上检测到具有功能活性的FcγR。仅在霍夫鲍尔细胞上检测到FcγRI(mAb 32.2)和FcγRIII(mAb 3G8),而在霍夫鲍尔细胞和内皮细胞上均检测到FcγRII(IV3和C1KM5)。霍夫鲍尔细胞、内皮细胞和滋养层细胞均表达FcγRIII(抗Leu - 11b)和IgG结合分子膜联蛋白II(mAb B1D6)。不同标本间染色存在一定差异,但从妊娠早期到中期,阳性细胞数量及染色强度均增加。在妊娠早期胎盘,染色定位于合体滋养层细胞和细胞滋养层细胞,细胞滋养层细胞及两层细胞交界处染色最强。在妊娠中期和晚期胎盘,染色定位于合体滋养层细胞。鉴于FcγR在IgG从母体转运至胎儿过程中的假定作用,其在胎盘发育过程中滋养层细胞上的定位和分布情况备受关注。

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