Maternal and Fetal Health Research Centre, Institute of Human Development, The University of Manchester, Manchester, UK.
Academic Health Science Centre, St Mary's Hospital, Manchester, UK.
Am J Reprod Immunol. 2019 Jan;81(1):e13054. doi: 10.1111/aji.13054. Epub 2018 Sep 29.
During pregnancy, the decidual spiral arterioles (SpAs) that supply maternal blood to the placenta undergo a series of changes to optimise the transfer of nutrients and oxygen to the developing foetus. Recent studies have shown that initiation of SpA transformation coincides with decidual leucocyte infiltration. Leucocytes are known to be a source of matrix metalloproteinases (MMPs); however, the complete profile of MMPs expressed by decidual NK cells (dNK) and macrophages has not been characterised. We hypothesised that leucocyte-derived MMPs contribute to SpA remodelling.
Decidual NK cells and macrophages were isolated from first trimester decidua and their MMP repertoire profiled by qRT-PCR (n = 10; 5-11 weeks). Dual immunofluorescence was used to localise MMP expression in situ (n = 3; 5-12 weeks). Gelatin zymography was carried out to assess whether leucocyte-derived MMPs can degrade ECM. In situ zymography and immunofluorescence identified MMP activity in tissue-resident dNK and macrophages.
Decidual NK cells cells and macrophages expressed MMP2, -7, -9, -11, -16, -19 and tissue inhibitors of metalloproteinase-1, -2, and -3. Both cell types degraded gelatin using MMP2 and MMP9 and broke down collagen in an in vitro model of the SpA. Extravillous trophoblasts (EVTs) expressed a similar repertoire of MMPs.
We suggest that matrix remodelling in SpA is initiated by infiltrating leucocytes, while EVTs become involved at later stages.
在妊娠期间,为胎盘提供母体血液的蜕膜螺旋动脉(SpA)经历一系列变化,以优化营养物质和氧气向发育中的胎儿的输送。最近的研究表明,SpA 转化的启动与蜕膜白细胞浸润同时发生。白细胞是基质金属蛋白酶(MMPs)的已知来源;然而,尚未对蜕膜自然杀伤细胞(dNK)和巨噬细胞表达的 MMP 完整谱进行特征描述。我们假设白细胞衍生的 MMPs 有助于 SpA 重塑。
从早孕期蜕膜中分离出 dNK 细胞和巨噬细胞,并通过 qRT-PCR 对其 MMP 谱进行分析(n=10;5-11 周)。通过双重免疫荧光原位定位 MMP 表达(n=3;5-12 周)。进行明胶酶谱分析以评估白细胞衍生的 MMP 是否可以降解 ECM。原位酶谱和免疫荧光鉴定了组织驻留的 dNK 和巨噬细胞中的 MMP 活性。
dNK 细胞和巨噬细胞表达 MMP2、-7、-9、-11、-16、-19 和金属蛋白酶组织抑制剂-1、-2 和 -3。两种细胞类型均使用 MMP2 和 MMP9 降解明胶,并在 SpA 的体外模型中破坏胶原蛋白。绒毛外滋养层(EVTs)表达相似的 MMP 谱。
我们认为 SpA 中的基质重塑是由浸润的白细胞引发的,而 EVTs 在后期才参与其中。