Yamamoto Madoka, Ikezaki Midori, Toujima Saori, Iwahashi Naoyuki, Mizoguchi Mika, Nanjo Sakiko, Minami Sawako, Ihara Yoshito, Ino Kazuhiko
Department of Obstetrics and Gynecology, Wakayama Medical University, Wakayama 641-0012, Japan.
Department of Biochemistry, Wakayama Medical University, Wakayama 641-0012, Japan.
Endocrinology. 2017 Nov 1;158(11):3874-3889. doi: 10.1210/en.2016-1966.
Calreticulin (CRT), a molecular chaperone in the endoplasmic reticulum (ER), plays a variety of roles in cell growth, differentiation, apoptosis, immunity, and cancer biology. It has been reported that CRT is expressed in the human placenta, although its function in placental development is poorly understood. Appropriate invasion of extravillous trophoblasts (EVTs) into the maternal decidua is necessary for successful pregnancy. The objective of the present study was to investigate the expression and functional role of CRT in EVTs using the human EVT cell line HTR8/SVneo, in which CRT gene expression was knocked down. We found that CRT was highly expressed in the human placenta in the early stage of pregnancy and localized to the EVTs. CRT knockdown markedly suppressed the invasion ability of HTR8/SVneo cells. Furthermore, the adhesion to fibronectin was suppressed in the CRT-knockdown cells via the dysfunction of integrin α5β1. In the CRT-knockdown cells, terminal sialylation and fucosylation were decreased, and the core galactose-containing structure was increased in the N-glycans of integrin β1. In addition, the expression levels of several critical glycosyltransferases were changed in the CRT-knockdown cells, consistent with the changes in the N-glycans. These results showed that CRT regulates the function of integrin β1 by affecting the synthesis of N-glycans in HTR8/SVneo cells. Collectively, the results of the present study demonstrate that the ER chaperone CRT plays a regulatory role in the invasion of EVTs, suggesting the importance of CRT expression in placental development during early pregnancy.
钙网蛋白(CRT)是内质网(ER)中的一种分子伴侣,在细胞生长、分化、凋亡、免疫和癌症生物学中发挥多种作用。据报道,CRT在人胎盘中表达,但其在胎盘发育中的功能尚不清楚。绒毛外滋养层细胞(EVT)向母体蜕膜的适当侵入是成功妊娠所必需的。本研究的目的是使用CRT基因表达被敲低的人EVT细胞系HTR8/SVneo来研究CRT在EVT中的表达及功能作用。我们发现CRT在妊娠早期的人胎盘中高度表达,并定位于EVT。CRT敲低显著抑制了HTR8/SVneo细胞的侵袭能力。此外,通过整合素α5β1功能障碍,CRT敲低细胞对纤连蛋白的黏附受到抑制。在CRT敲低细胞中,整合素β1的N-聚糖末端唾液酸化和岩藻糖基化减少,含核心半乳糖的结构增加。此外,CRT敲低细胞中几种关键糖基转移酶的表达水平发生了变化,与N-聚糖的变化一致。这些结果表明,CRT通过影响HTR8/SVneo细胞中N-聚糖的合成来调节整合素β1的功能。总体而言,本研究结果表明内质网伴侣CRT在EVT侵袭中起调节作用,提示CRT表达在妊娠早期胎盘发育中的重要性。