Kamper Miriam, Mittermayer Florian, Cabuk Rosalinda, Gelles Katharina, Ellinger Isabella, Hermann Marcela
Department of Medical Biochemistry, Max F. Perutz Laboratories (MFPL), Medical University of Vienna, Vienna, Austria.
Institute for Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.
Biochimie. 2017 Jul;138:116-123. doi: 10.1016/j.biochi.2017.05.006. Epub 2017 May 6.
Cholesterol is an important nutrient for fetal development and transplacental transport occurs at all stages of human pregnancy. Furthermore, cholesterol is required for membrane building as well as steroid hormone synthesis. Therefore, all placental cell types require cholesterol for proper function. In human term placenta, the syncytiotrophoblast (STB) faces the maternal circulation. Uptake of maternal-derived cholesterol at the apical membrane of the STB is well understood, but the route by which cholesterol exits at the basal side for subsequent transfer across the fetal endothelial cells (FEC) or to other placental cell types remains not well characterized. Our aim was to provide evidence for basal secretion of apolipoprotein B-100 (apoB) containing lipoproteins. Furthermore, we investigated the placental localization of apolipoprotein receptors (LRP2, LDLR and LRP1) to identify cell targets of lipoprotein particles secreted in a polarized fashion by the STB. In trophoblast-derived BeWo cells grown on permeable filter supports, we demonstrate by immunoprecipitation apical as well as basolateral apoB secretion, which was significantly upregulated by estrogen-treatment for 24 or 48 h. Furthermore, we showed by immunofluorescence microscopy apoB and microsomal triglyceride transfer protein subunits localization in the STB and placental stromal cells in situ. All investigated receptors were detected by RT-qPCR and western blot in BeWo cells, but only expression of LRP2 was estrogen-inducible. In situ, the multi-ligand receptor LRP2 was expressed exclusively in the cytotrophoblast (CTB), the STB precursor cell type. LDLR and LRP1 localized to trophoblasts as well as stromal cells in situ. In summary, basal apoB secretion by BeWo cells supports the concept of basal lipoprotein particle secretion by placental STB. These lipoprotein particles may serve as cholesterol source for STB precursor cells, the CTBs, as well as all stromal cells of the chorionic villi including FECs, which were herein demonstrated to express apoB receptors, LRP2 and LDLR, respectively.
胆固醇是胎儿发育的重要营养素,在人类妊娠的各个阶段都会发生跨胎盘转运。此外,细胞膜构建和类固醇激素合成都需要胆固醇。因此,所有胎盘细胞类型正常发挥功能都需要胆固醇。在足月人类胎盘中,合体滋养层细胞(STB)面向母体循环。STB顶端膜摄取母体来源的胆固醇已为人熟知,但胆固醇从基底侧排出以便随后穿过胎儿内皮细胞(FEC)或转运至其他胎盘细胞类型的途径仍未得到充分描述。我们的目的是为含载脂蛋白B - 100(apoB)的脂蛋白的基底分泌提供证据。此外,我们研究了载脂蛋白受体(LRP2、LDLR和LRP1)在胎盘的定位,以确定由STB以极化方式分泌的脂蛋白颗粒的细胞靶点。在生长于可渗透滤膜支架上的滋养层来源的BeWo细胞中,我们通过免疫沉淀证明了顶端和基底外侧的apoB分泌,雌激素处理24或48小时后其分泌显著上调。此外,我们通过免疫荧光显微镜观察了原位STB和胎盘基质细胞中apoB和微粒体甘油三酯转移蛋白亚基的定位。通过RT - qPCR和蛋白质免疫印迹法在BeWo细胞中检测到了所有研究的受体,但只有LRP2的表达可被雌激素诱导。在原位,多配体受体LRP2仅在细胞滋养层细胞(CTB)中表达,CTB是STB的前体细胞类型。LDLR和LRP1在原位定位于滋养层细胞以及基质细胞。总之,BeWo细胞的基底apoB分泌支持了胎盘STB基底脂蛋白颗粒分泌的概念。这些脂蛋白颗粒可能作为STB前体细胞CTB以及绒毛膜绒毛所有基质细胞(包括在此证明分别表达apoB受体LRP2和LDLR的FEC)的胆固醇来源。