Comparison of Organoids from Menstrual Fluid and Hormone-Treated Endometrium: Novel Tools for Gynecological Research.
Caitlin E FilbyKatherine A WyattSally MortlockFiona L CousinsBrett McKinnonKate E TysonGrant W MontgomeryCaroline E GargettPublished in: Journal of personalized medicine (2021)
Endometrial organoids (EMO) are an important tool for gynecological research but have been limited by generation from (1) invasively acquired tissues and thus advanced disease states and (2) from women who are not taking hormones, thus excluding 50% of the female reproductive-aged population. We sought to overcome these limitations by generating organoids from (1) menstrual fluid (MF; MFO) using a method that enables the concurrent isolation of menstrual fluid supernatant, stromal cells, and leukocytes and (2) from biopsies and hysterectomy samples from women taking hormonal medication (EMO-H). MF was collected in a menstrual cup for 4-6 h on day 2 of menstruation. Biopsies and hysterectomies were obtained during laparoscopic surgery. Organoids were generated from all sample types, with MFO and EMO-H showing similar cell proliferation rates, proportion and localization of the endometrial basalis epithelial marker, Stage Specific Embryonic Antigen-1 (SSEA-1), and gene expression profiles. Organoids from different disease states showed the moderate clustering of epithelial secretory and androgen receptor signaling genes. Thus, MFO and EMO-H are novel organoids that share similar features to EMO but with the advantage of (1) MFO being obtained non-invasively and (2) EMO-H being obtained from 50% of the women who are not currently being studied through standard methods. Thus, MFO and EMO-H are likely to prove to be invaluable tools for gynecological research, enabling the population-wide assessment of endometrial health and personalized medicine.
Keyphrases
- polycystic ovary syndrome
- induced pluripotent stem cells
- cell proliferation
- healthcare
- laparoscopic surgery
- genome wide
- pregnancy outcomes
- endometrial cancer
- public health
- gene expression
- metabolic syndrome
- radiation therapy
- single cell
- insulin resistance
- high intensity
- breast cancer risk
- dna methylation
- copy number
- squamous cell carcinoma
- adipose tissue
- pregnant women
- skeletal muscle
- social media
- cell free
- ultrasound guided
- health information
- climate change
- genome wide analysis