Upregulated CXCL8 in placenta accreta spectruma regulates the migration and invasion of HTR-8/SVneo cells

• Published in: Molecular biology reports 2023-10, Vol.50 (10), p.8189-8199
• Main Authors: Chen, Yuejuan, Zou, Ping, Bu, Chaozhi, Jiang, Qianying, Xue, Lili, Bao, Junfeng, Zhang, Ting
• Format: Article
• Language: English
• Subjects: Animal Anatomy; Animal Biochemistry; Biomedical and Life Sciences; Blood vessels; Cell migration; Chemokines; Childrens health; E-cadherin; Gene expression; Genes; Genomes; Histology; Hospitals; Immune system; Life Sciences; Ligands; Matrix metalloproteinase; Metalloproteinase; Molecular biology; Morphology; mRNA; Ontology; Original Article; Placenta; Pregnancy; Signal transduction; Therapeutic targets; Tumors; Western blotting; Wnt protein; Womens health
• ISSN: 0301-4851; 1573-4978
• DOI: 10.1007/s11033-023-08669-x

Background 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. Methods 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. Results 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. Conclusions 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.