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早期妊娠胎盘绒毛外滋养层细胞表面CD1d的表达以依赖于滋养层分化的方式下调。

Expression of surface CD1d in the extravillous trophoblast cells of early gestational placenta is downregulated in a manner dependent on trophoblast differentiation.

作者信息

Matsumoto Junko, Kawana Kei, Nagamatsu Takeshi, Schust Danny J, Fujii Tomoyuki, Sato Hidetaka, Hyodo Hironobu, Yasugi Toshiharu, Kozuma Shiro, Taketani Yuji

机构信息

Department of Obstetrics and Gynecology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.

出版信息

Biochem Biophys Res Commun. 2008 Jun 27;371(2):236-41. doi: 10.1016/j.bbrc.2008.04.051. Epub 2008 Apr 21.

Abstract

CD1d is a specific ligand for the invariant Valpha24Vbeta11-natural killer T (iNKT) cells that play an important role in placental development during early human pregnancy. The localization and regulation of placental CD1d expression remain unclear. Immunohistochemistry of human early gestational placentas revealed CD1d was present in villous and extravillous trophoblast (EVT) but not in syncytiotrophoblast or decidual cells. CD1d immunoreactivity in EVT cells decreased with EVT differentiation. Flow cytometry of primary cultured human trophoblast cells confirmed cell-surface expression of CD1d decreased with time in culture. These changes in CD1d expression occur at the level of transcription. TGF-beta1 secreted from the cultured EVT cells accumulated with time in culture and directly suppressed CD1d expression, as evidenced by monoclonal antibody neutralization of TGF-beta1 effects. Thus, trophoblast differentiation is characterized by TGF-beta1-mediated decreases in trophoblast cell CD1d expression. This effect may support appropriate activation of decidual iNKT cells at the maternal-fetal interface.

摘要

CD1d是恒定链α24β11自然杀伤T(iNKT)细胞的特异性配体,iNKT细胞在人类妊娠早期的胎盘发育中起重要作用。胎盘CD1d表达的定位和调节仍不清楚。对人类早期妊娠胎盘的免疫组织化学分析显示,CD1d存在于绒毛和绒毛外滋养层(EVT)中,但不存在于合体滋养层或蜕膜细胞中。EVT细胞中的CD1d免疫反应性随EVT分化而降低。对原代培养的人类滋养层细胞进行流式细胞术分析证实,细胞表面CD1d的表达随培养时间而降低。CD1d表达的这些变化发生在转录水平。培养的EVT细胞分泌的转化生长因子β1(TGF-β1)随培养时间而积累,并直接抑制CD1d表达,TGF-β1效应的单克隆抗体中和证明了这一点。因此,滋养层分化的特征是TGF-β1介导的滋养层细胞CD1d表达降低。这种效应可能有助于在母胎界面适当激活蜕膜iNKT细胞。

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