Differential gene expression in decidualized human endometrial stromal cells induced by different stimuli.
Yumiko Doi-TanakaIsao TamuraAmon ShiroshitaTaishi FujimuraYuichiro ShirafutaRyo MaekawaToshiaki TaketaniShun SatoNorihiro SuginoPublished in: Scientific reports (2024)
Decidualization can be induced by culturing human endometrial stromal cells (ESCs) with several decidualization stimuli, such as cAMP, medroxyprogesterone acetate (MPA) or Estradiol (E 2 ). However, it has been unclear how decidualized cells induced by different stimuli are different. We compared transcriptomes and cellular functions of decidualized ESCs induced by different stimuli (MPA, E 2 + MPA, cAMP, and cAMP + MPA). We also investigated which decidualization stimulus induces a closer in vivo decidualization. Differentially expressed genes (DEGs) and altered cellular functions by each decidualization stimuli were identified by RNA-sequence and gene-ontology analysis. DEGs was about two times higher for stimuli that use cAMP (cAMP and cAMP + MPA) than for stimuli that did not use cAMP (MPA and E 2 + MPA). cAMP-using stimuli altered the cellular functions including angiogenesis, inflammation, immune system, and embryo implantation whereas MPA-using stimuli (MPA, E 2 + MPA, and cAMP + MPA) altered the cellular functions associated with insulin signaling. A public single-cell RNA-sequence data of the human endometrium was utilized to analyze in vivo decidualization. The altered cellular functions by in vivo decidualization were close to those observed by cAMP + MPA-induced decidualization. In conclusion, decidualized cells induced by different stimuli have different transcriptome and cellular functions. cAMP + MPA may induce a decidualization most closely to in vivo decidualization.
Keyphrases
- binding protein
- endothelial cells
- gene expression
- protein kinase
- single cell
- oxidative stress
- genome wide
- emergency department
- healthcare
- high glucose
- mental health
- cell death
- adipose tissue
- high resolution
- machine learning
- pluripotent stem cells
- cell cycle arrest
- mass spectrometry
- electronic health record
- transcription factor
- drug induced
- skeletal muscle
- stress induced
- artificial intelligence
- adverse drug