Chau K, Xu B, Hennessy A, Makris A
Vascular Immunology Group, Heart Research Institute, Sydney, Australia.
School of Medicine, Western Sydney University, Sydney, Australia.
Reprod Sci. 2020 Jun;27(6):1285-1292. doi: 10.1007/s43032-019-00103-7. Epub 2020 Feb 3.
Placental growth factor (PlGF) is an important angiogenic factor which has an emerging role in the clinical management of suspected preeclampsia. The role of PlGF in normal placental development is not completely understood and it is uncertain whether PlGF influences trophoblast and endothelial cell interactions central to uterine spiral artery remodelling, especially in variable oxygen conditions. A two-cell model of endovascular invasion was used. Tissue culture plates were coated with Matrigel™, on which fluorescent-labelled uterine microvascular endothelial cells (1 × 10/well) and HTR8/SVNeo cells were co-cultured (1 × 10/well) for 20 h. Co-cultures were treated with recombinant human PlGF (rhPlGF) (10 or 100 ng/mL) and incubated at either 21% O or 2% O. Images were captured by fluorescence microscopy and analysed using ImageJ (n = 7). Data was analysed using SPSSv24. Treatment with rhPlGF did not improve integration in co-cultures irrespective of oxygen conditions but increased proliferation in 2% O of both trophoblast and endothelial cells. Expression of angiogenic factors VEGF, sFLT-1, PlGF and CXCL12 in both co-cultures and in isolated trophoblast cells was not altered by rhPlGF treatment. Expression of TLR-3 mRNA in co-cultures was increased by rhPlGF 100 ng/mL at 21% O (p = 0.03). PlGF contributes to trophoblast and endothelial cell proliferation in the setting of physiological hypoxia but does not influence trophoblast and endothelial cell interactions in an in vitro model of spiral artery remodelling. Upregulation of TLR-3 expression in co-cultures may indicate a role for PlGF in the placental inflammatory response.
胎盘生长因子(PlGF)是一种重要的血管生成因子,在疑似子痫前期的临床管理中发挥着越来越重要的作用。PlGF在正常胎盘发育中的作用尚未完全明确,其是否影响子宫螺旋动脉重塑所必需的滋养层细胞与内皮细胞的相互作用尚不确定,尤其是在不同氧环境下。本研究采用血管内侵入的双细胞模型。将组织培养板用基质胶包被,在其上共培养荧光标记的子宫微血管内皮细胞(1×10/孔)和HTR8/SVNeo细胞(1×10/孔)20小时。共培养物用重组人PlGF(rhPlGF)(10或100 ng/mL)处理,并在21% O₂或2% O₂条件下孵育。通过荧光显微镜拍摄图像,并使用ImageJ进行分析(n = 7)。数据采用SPSSv24进行分析。无论氧环境如何,rhPlGF处理均未改善共培养物中的整合,但在2% O₂条件下增加了滋养层细胞和内皮细胞的增殖。rhPlGF处理未改变共培养物和分离的滋养层细胞中血管生成因子VEGF、sFLT-1、PlGF和CXCL12的表达。在21% O₂条件下,100 ng/mL的rhPlGF可使共培养物中TLR-3 mRNA的表达增加(p = 0.03)。在生理性缺氧条件下,PlGF有助于滋养层细胞和内皮细胞的增殖,但在螺旋动脉重塑的体外模型中不影响滋养层细胞与内皮细胞的相互作用。共培养物中TLR-3表达的上调可能表明PlGF在胎盘炎症反应中发挥作用。