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胎盘基底层膜蛋白是三维生物打印胎盘模型中有效滋养细胞侵袭所必需的。

Placental basement membrane proteins are required for effective cytotrophoblast invasion in a three-dimensional bioprinted placenta model.

机构信息

Fischell Department of Bioengineering, University of Maryland, College Park, Maryland, 20740.

Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Health System, Washington, District of Columbia, 20010.

出版信息

J Biomed Mater Res A. 2018 Jun;106(6):1476-1487. doi: 10.1002/jbm.a.36350. Epub 2018 Feb 6.

Abstract

Fetal cytotrophoblast invasion of maternal decidual vasculature is necessary to normal pregnancy. In preeclampsia, there is shallow invasion and abnormal remodeling of the uterine vasculature that lead to significant maternal and perinatal morbidity and mortality. The placental basement membrane (BM) proteins (e.g., laminin and collagen) has been implicated in the development of placenta while the level of laminin is significantly lower in preeclampsia. However, there are very limited studies, if any, on the effect of extracellular matrix (ECM) microenvironment on the invasion of cytotrophoblast. In this study, we hypothesized that placental BM proteins are required for effective cytotrophoblast invasion. Using proteomics, we found that more than 80% of ECM proteins in placental basal plate (pECM) were BM proteins. In addition to upregulating expressions of MMP2 (1.5-fold) and MMP9 (6.3-fold), pECM significantly increased the motility rates of cytotrophoblasts by 13-fold (from 5.60 ± 0.95 to 75.5 ± 21.8 µm/day) to achieve an effective invasion rate that was comparable to in vivo results. Treatments with PI3K inhibitors completely removed the pECM-enhanced invasive phenotypes and genotypes of cytotrophoblasts, suggesting its dominant role in cytotrophoblast-ECM interactions. Our results described, for the first time, the substantial effects of the ECM microenvironment on regulating cytotrophoblast invasion, an area that is less investigated but appear to be critical in the pathogenesis of preeclampsia. Moreover, the approach presented in this work that fabricates organ models with organ-specific ECM can be an attractive option to screen and develop novel therapeutics and biomarkers not only in preeclampsia but also other diseases such as cancer metastasis. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 1476-1487, 2018.

摘要

滋养细胞侵入母体蜕膜血管对于正常妊娠是必要的。在子痫前期,子宫血管的侵入和异常重塑导致显著的母亲和围产期发病率和死亡率。胎盘基底膜 (BM) 蛋白(例如层粘连蛋白和胶原)已被牵连到胎盘的发育中,而子痫前期的层粘连蛋白水平显著降低。然而,关于细胞外基质 (ECM) 微环境对滋养细胞侵入的影响的研究非常有限,如果有的话。在这项研究中,我们假设胎盘 BM 蛋白是有效滋养细胞侵入所必需的。通过蛋白质组学,我们发现胎盘基板 (pECM) 中超过 80%的 ECM 蛋白是 BM 蛋白。除了上调 MMP2(1.5 倍)和 MMP9(6.3 倍)的表达外,pECM 还使滋养细胞的迁移率显著增加 13 倍(从 5.60±0.95 至 75.5±21.8 µm/天),以达到与体内结果相当的有效侵入率。PI3K 抑制剂的处理完全消除了 pECM 增强的滋养细胞侵入表型和基因型,表明其在滋养细胞-ECM 相互作用中起主导作用。我们的结果首次描述了 ECM 微环境对调节滋养细胞侵入的实质性影响,该领域的研究较少,但在子痫前期的发病机制中似乎至关重要。此外,本工作提出的用器官特异性 ECM 制造器官模型的方法不仅在子痫前期,而且在癌症转移等其他疾病中筛选和开发新型治疗剂和生物标志物可能是一种有吸引力的选择。© 2018 威利父子公司

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07fe/5924478/afc238bfcb06/nihms937119f1.jpg

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