Abbas Yassen, Carnicer-Lombarte Alejandro, Gardner Lucy, Thomas Jake, Brosens Jan J, Moffett Ashley, Sharkey Andrew M, Franze Kristian, Burton Graham J, Oyen Michelle L
The Nanoscience Centre, Department of Engineering, University of Cambridge, Cambridge CB3 0FF, UK.
Department of Pathology, University of Cambridge, Cambridge CB2 1QP, UK.
Hum Reprod. 2019 Oct 2;34(10):1999-2008. doi: 10.1093/humrep/dez139.
What is the stiffness (elastic modulus) of human nonpregnant secretory phase endometrium, first trimester decidua, and placenta?
The stiffness of decidua basalis, the site of placental invasion, was an order of magnitude higher at 103 Pa compared to 102 Pa for decidua parietalis, nonpregnant endometrium and placenta.
Mechanical forces have profound effects on cell behavior, regulating both cell differentiation and migration. Despite their importance, very little is known about their effects on blastocyst implantation and trophoblast migration during placental development because of the lack of mechanical characterization at the human maternal-fetal interface.
STUDY DESIGN, SIZE, DURATION: An observational study was conducted to measure the stiffness of ex vivo samples of human nonpregnant secretory endometrium (N = 5) and first trimester decidua basalis (N = 6), decidua parietalis (N = 5), and placenta (N = 5). The stiffness of the artificial extracellular matrix (ECM), Matrigel®, commonly used to study migration of extravillous trophoblast (EVT) in three dimensions and to culture endometrial and placental organoids, was also determined (N = 5).
PARTICIPANTS/MATERIALS, SETTING, METHODS: Atomic force microscopy was used to perform ex vivo direct measurements to determine the stiffness of fresh tissue samples. Decidua was stained by immunohistochemistry (IHC) for HLA-G+ EVT to confirm whether samples were decidua basalis or decidua parietalis. Endometrium was stained with hematoxylin and eosin to confirm the presence of luminal epithelium. Single-cell RNA sequencing data were analyzed to determine expression of ECM transcripts by decidual and placental cells. Fibrillin 1, a protein identified by these data, was stained by IHC in decidua basalis.
We observed that decidua basalis was significantly stiffer than decidua parietalis, at 1250 and 171 Pa, respectively (P < 0.05). The stiffness of decidua parietalis was similar to nonpregnant endometrium and placental tissue (250 and 232 Pa, respectively). These findings suggest that it is the presence of invading EVT that is driving the increase in stiffness in decidua basalis. The stiffness of Matrigel® was found to be 331 Pa, significantly lower than decidua basalis (P < 0.05).
N/A.
LIMITATIONS, REASONS FOR CAUTION: Tissue stiffness was derived by ex vivo measurements on blocks of fresh tissue in the absence of blood flow. The nonpregnant endometrium samples were obtained from women undergoing treatment for infertility. These may not reflect the stiffness of endometrium from normal fertile women.
These results provide direct measurements of tissue stiffness during the window of implantation and first trimester of human pregnancy. They serve as a basis of future studies exploring the impact of mechanics on embryo implantation and development of the placenta. The findings provide important baseline data to inform matrix stiffness requirements when developing in vitro models of trophoblast stem cell development and migration that more closely resemble the decidua in vivo.
STUDY FUNDING/COMPETING INTEREST(S): This work was supported by the Centre for Trophoblast Research, the Wellcome Trust (090108/Z/09/Z, 085992/Z/08/Z), the Medical Research Council (MR/P001092/1), the European Research Council (772426), an Engineering and Physical Sciences Research Council Doctoral Training Award (1354760), a UK Medical Research Council and Sackler Foundation Doctoral Training Grant (RG70550) and a Wellcome Trust Doctoral Studentship (215226/Z/19/Z).
人类非孕分泌期子宫内膜、孕早期蜕膜及胎盘的硬度(弹性模量)是多少?
胎盘植入部位的基蜕膜硬度比壁蜕膜、非孕子宫内膜及胎盘高一个数量级,分别为10³帕斯卡和10²帕斯卡。
机械力对细胞行为有深远影响,可调节细胞分化和迁移。尽管其很重要,但由于缺乏对人类母胎界面的力学特性研究,人们对其在胎盘发育过程中对囊胚着床和滋养层迁移的影响知之甚少。
研究设计、规模、持续时间:进行了一项观察性研究,以测量人类非孕分泌期子宫内膜(N = 5)、孕早期基蜕膜(N = 6)、壁蜕膜(N = 5)及胎盘(N = 5)的离体样本的硬度。还测定了常用于研究三维绒毛外滋养层(EVT)迁移及培养子宫内膜和胎盘类器官的人工细胞外基质(ECM)基质胶的硬度(N = 5)。
参与者/材料、设置、方法:使用原子力显微镜进行离体直接测量,以确定新鲜组织样本的硬度。通过免疫组织化学(IHC)对蜕膜进行HLA - G⁺ EVT染色,以确认样本是基蜕膜还是壁蜕膜。用苏木精和伊红对子宫内膜进行染色,以确认腔上皮的存在。分析单细胞RNA测序数据,以确定蜕膜和胎盘细胞中ECM转录本的表达。通过这些数据鉴定出的一种蛋白质原纤维蛋白1,在基蜕膜中进行IHC染色。
我们观察到,基蜕膜的硬度明显高于壁蜕膜,分别为1250和171帕斯卡(P < 0.05)。壁蜕膜的硬度与非孕子宫内膜和胎盘组织相似(分别为250和232帕斯卡)。这些发现表明,正是侵入性EVT的存在导致了基蜕膜硬度的增加。发现基质胶的硬度为331帕斯卡,明显低于基蜕膜(P < 0.05)。
无。
局限性、谨慎原因:组织硬度是通过对无血流的新鲜组织块进行离体测量得出的。非孕子宫内膜样本取自接受不孕症治疗的女性。这些样本可能无法反映正常育龄女性子宫内膜的硬度。
这些结果提供了人类妊娠着床期和孕早期组织硬度的直接测量值。它们为未来探索力学对胚胎着床和胎盘发育影响的研究奠定了基础。这些发现提供了重要的基线数据,以便在开发更类似于体内蜕膜的滋养层干细胞发育和迁移的体外模型时,确定基质硬度要求。
研究资金/竞争利益:这项工作得到了滋养层研究中心、惠康信托基金会(090108/Z/09/Z,085992/Z/08/Z)、医学研究理事会(MR/P001092/1)、欧洲研究理事会(772426)、工程和物理科学研究理事会博士培训奖(1354760)、英国医学研究理事会和萨克勒基金会博士培训资助(RG70550)以及惠康信托基金会博士奖学金(215226/Z/19/Z)的支持。