Saji F, Samejima Y, Kamiura S, Koyama M
Department of Gynecology, Osaka Medical Center for Cancer and Cardiovascular Diseases, Japan.
Rev Reprod. 1999 May;4(2):81-9. doi: 10.1530/ror.0.0040081.
Transplacental transport of maternal immunoglobulin G (IgG) to the developing fetus is extremely important in the protection of the newborn from infection. Although the exact mechanisms of the selective and active transfer of IgG across the placental barrier are not fully understood, receptors for the Fc part of IgG (FcgammaRs) in the placenta are believed to play a key role. Several known Fc receptors, FcgammaRI, FcgammaRII, FcgammaRIII and FcRn (neonatal FcR), demonstrate heterogeneous expression patterns in placenta. Immunohistochemical analysis shows the expression of FcgammaRI on Hofbauer cells in stromal tissue, FcbetaRII on Hofbauer cells and fetal blood endothelium, FcgammaRIII on Hofbauer cells and trophoblasts, and FcRn on syncytiotrophoblasts and endothelial cells. Recent studies provide evidence for important associations among these receptors and transcytosis of IgG, as well as scavenger mechanisms for clearing immune complexes in the placenta during pregnancy.
母体免疫球蛋白G(IgG)经胎盘转运至发育中的胎儿,这对于保护新生儿免受感染极为重要。尽管IgG跨胎盘屏障进行选择性和主动转运的确切机制尚未完全明确,但胎盘内IgG的Fc段受体(FcγRs)被认为起着关键作用。几种已知的Fc受体,即FcγRI、FcγRII、FcγRIII和FcRn(新生儿Fc受体),在胎盘中呈现出异质性表达模式。免疫组织化学分析显示,FcγRI在基质组织的霍夫鲍尔细胞上表达,FcβRII在霍夫鲍尔细胞和胎儿血液内皮细胞上表达,FcγRIII在霍夫鲍尔细胞和成滋养层细胞上表达,而FcRn在合体滋养层细胞和内皮细胞上表达。最近的研究为这些受体与IgG的转胞吞作用之间的重要关联,以及孕期胎盘内清除免疫复合物的清除机制提供了证据。