Wuxi Maternity and Child Health Care Hospital, Women's Hospital of Jiangnan University, Jiangnan University, Wuxi, 214002, China.
Mol Biol Rep. 2023 Oct;50(10):8189-8199. doi: 10.1007/s11033-023-08669-x. Epub 2023 Aug 10.
Placenta accreta spectrum (PAS) is mainly characterized by excessive invasion of the uterine muscle layer accompanied by a large number of foreign blood vessels, leading to severe bleeding during and after delivery. However, the mechanism of excessive invasion of nutrient cells in placenta accreta is currently unclear.
We performed RNA sequencing of 6 PAS patients and 4 control donors, coupled with Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. The mRNA and protein expression of C-X-C motif ligand 8 (CXCL8) in the placental tissue was measured by qRT‒PCR, immunohistochemical staining and Western blotting. HTR-8/SVneo human villous trophoblast Neo cells were used for in vitro investigation of cell migration and invasion as well as the expression level of CXCL8.
A total of 1120 differentially expressed mRNAs were identified in PAS patients. Moreover, GO and KEGG analyses indicated that the differentially expressed mRNAs were most closely associated with immune system processes, biological adhesion and Wnt signaling pathway. The CXCL8 mRNA and protein levels in PAS tissue were significantly higher than those in normal placental tissue. Forced overexpression of CXCL8 significantly increased the migration and invasion of HTR-8/SVneo cells, accompanied by the upregulation of matrix metalloproteinase-2 and matrix metalloproteinase-9 and the downregulation of E-cadherin, which was reversed by knockdown of CXCL8.
CXCL8 was highly expressed in PAS, and knockdown of CXCL8 suppressed the migration and invasion of HTR-8/SVneo cells, suggesting its potential as a diagnostic and therapeutic target for PAS.
胎盘部位滋养细胞肿瘤谱(PAS)的主要特征是滋养细胞过度侵入子宫肌层,并伴有大量新生血管,导致分娩中和分娩后大量出血。然而,胎盘部位滋养细胞过度侵入的机制目前尚不清楚。
我们对 6 名 PAS 患者和 4 名对照供体进行了 RNA 测序,并进行了基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析。通过 qRT-PCR、免疫组织化学染色和 Western blot 检测胎盘组织中 C-X-C 基序配体 8(CXCL8)的 mRNA 和蛋白表达。体外研究了 HTR-8/SVneo 人绒毛滋养层 Neo 细胞的迁移和侵袭以及 CXCL8 的表达水平。
在 PAS 患者中鉴定出 1120 个差异表达的 mRNA。此外,GO 和 KEGG 分析表明,差异表达的 mRNAs 与免疫系统过程、生物黏附和 Wnt 信号通路最密切相关。PAS 组织中的 CXCL8 mRNA 和蛋白水平明显高于正常胎盘组织。过表达 CXCL8 显著增加了 HTR-8/SVneo 细胞的迁移和侵袭,同时上调了基质金属蛋白酶-2 和基质金属蛋白酶-9,下调了 E-钙黏蛋白,而 CXCL8 的敲低则逆转了这一过程。
CXCL8 在 PAS 中高表达,敲低 CXCL8 抑制了 HTR-8/SVneo 细胞的迁移和侵袭,提示其可能成为 PAS 的诊断和治疗靶点。