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人胎盘发育过程中滋养层细胞上Fcγ受体的分布:一项免疫组织化学和免疫印迹研究

Distribution of Fc gamma receptors on trophoblast during human placental development: an immunohistochemical and immunoblotting study.

作者信息

Wainwright S D, Holmes C H

机构信息

University of Bristol, Department of Obstetrics and Gynaecology, St Michael's Hospital.

出版信息

Immunology. 1993 Nov;80(3):343-51.

Abstract

Expression of Fc gamma receptors on human placental trophoblast was investigated by immunostaining and immunoblotting using a panel of Fc gamma receptor monoclonal antibodies (mAb). Fc gamma receptors typical of other cell types were not detected on syncytiotrophoblast in term placentae when transplacental IgG transport was maximal. Unexpectedly, however, and by contrast with term, all Fc gamma receptor III mAb tested bound to first trimester placental syncytiotrophoblast by immunostaining. Reactivity was relatively restricted and varied between specimens. Fc gamma receptor III products of 41,000-45,000 and 49,000-52,000 MW were consistently detected on first trimester trophoblast membranes by immunoblotting and levels of these products were greatly reduced following treatment with phosphatidylinositol-specific phospholipase C, suggesting that the early trophoblast Fc gamma receptor III is glycosyl-phosphatidylinositol (GPI) linked. The mAb Leu-11b behaved differently to other anti-Fc gamma receptor III mAb examined. By immunostaining, Leu-11b bound to syncytiotrophoblast at term and detected both syncytiotrophoblast and underlying cytotrophoblast in the first trimester. In addition to the GPI-anchored Fc gamma receptor III in first trimester, Leu-11b also detected a 74,000 MW component on both first trimester and term trophoblast membranes by immunoblotting. Thus trophoblast appears to express a GPI-anchored Fc gamma receptor III in first trimester but not term placentae. With the exception of the 74,000 MW Leu-11b-defined product whose function is unclear, currently available Fc gamma receptor mAb appear to be incapable of detecting the protein involved in IgG transport during the later stages of gestation.

摘要

利用一组Fcγ受体单克隆抗体(mAb),通过免疫染色和免疫印迹法研究了人胎盘滋养层细胞上Fcγ受体的表达情况。在足月胎盘经胎盘IgG转运达到最大值时,未在合体滋养层细胞上检测到其他细胞类型典型的Fcγ受体。然而,出乎意料的是,与足月胎盘形成对比的是,通过免疫染色检测,所有测试的Fcγ受体III型单克隆抗体都与孕早期胎盘合体滋养层细胞结合。反应性相对受限,且不同标本之间存在差异。通过免疫印迹法在孕早期滋养层细胞膜上持续检测到分子量为41,000 - 45,000和49,000 - 52,000的Fcγ受体III型产物,用磷脂酰肌醇特异性磷脂酶C处理后,这些产物的水平大幅降低,这表明早期滋养层细胞的Fcγ受体III型是糖基磷脂酰肌醇(GPI)连接的。单克隆抗体Leu - 11b的表现与其他检测的抗Fcγ受体III型单克隆抗体不同。通过免疫染色,Leu - 11b在足月时与合体滋养层细胞结合,并在孕早期检测到合体滋养层细胞和其下方的细胞滋养层细胞。除了孕早期的GPI锚定的Fcγ受体III型外,Leu - 11b通过免疫印迹法还在孕早期和足月滋养层细胞膜上检测到一种74,000分子量的成分。因此,滋养层细胞在孕早期似乎表达GPI锚定的Fcγ受体III型,而足月胎盘则不表达。除了功能尚不清楚的74,000分子量的Leu - 11b定义产物外,目前可用的Fcγ受体单克隆抗体似乎无法检测到妊娠后期参与IgG转运的蛋白质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9018/1422222/d190c0b9ff74/immunology00090-0011-a.jpg

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