Choriodecidual leukocytes display a unique gene expression signature in spontaneous labor at term.
Marcia Arenas-HernandezNardhy Gomez-LopezValeria Garcia-FloresClaudia Rangel-EscareñoLuis M Alvarez-SalasNatalia Martinez-AcuñaJoel A Vazquez-PerezRodrigo Vega-SanchezPublished in: Genes and immunity (2018)
Prior to and during the process of human labor, maternal circulating leukocytes infiltrate the maternal-fetal interface (choriodecidua) and become activated resembling choriodecidual leukocytes. Since, there is no evidence comparing maternal circulating and choriodecidual leukocytes, herein, we characterized their transcriptome and explored the biological processes enriched in choriodecidual leukocytes. From women undergoing spontaneous term labor we isolated circulating and choriodecidual leukocytes, performed microarray analysis (n = 5) and qRT-PCR validation (n = 9) and interaction network analysis with up-regulated genes. We found 270 genes up-regulated and only 17 genes down-regulated in choriodecidual leukocytes compared to maternal circulating leukocytes. The most up-regulated genes were CCL18, GPNMB, SEPP1, FN1, RNASE1, SPP1, C1QC, and PLTP. The biological processes enriched in choriodecidual leukocytes were cell migration and regulation of immune response, chemotaxis, and humoral immune responses. Our results show striking differences between the transcriptome of choriodecidual and maternal circulating leukocytes. Choriodecidual leukocytes are enriched in immune mediators implicated in the spontaneous process of labor at term.
Keyphrases
- peripheral blood
- immune response
- gene expression
- genome wide
- birth weight
- pregnancy outcomes
- transcription factor
- gestational age
- preterm infants
- cell migration
- dna methylation
- network analysis
- endothelial cells
- bioinformatics analysis
- body mass index
- toll like receptor
- pregnant women
- skeletal muscle
- inflammatory response
- liver injury
- preterm birth
- drug induced
- genome wide analysis