TY - JOUR
T1 - Endometrial stem/progenitor cells in menstrual blood and peritoneal fluid of women with and without endometriosis
AU - Masuda, Hirotaka
AU - Schwab, Kjiana E.
AU - Filby, C. E.
AU - Tan, Charmaine S.C.
AU - Tsaltas, Jim
AU - Weston, Gareth C.
AU - Gargett, Caroline E.
N1 - Funding Information:
This work was supported by the Australian National Health and Medical Research Council (grant numbers 545992, 104229, 1173882), the Royal Australian and New Zealand College of Obstetrics and Gynaecology (RANZCOG) Ella Macknight Memorial Scholarship, an Australian Postgraduate Award and the Victorian Government's Operational Infrastructure Support Program. The authors would like to thank the Ritchie Centre Tissue Bank research nurses, Ms. Grace Heo, Erica O'Donoghue, Pam Mamers, Germana Ryan and Yao Han, for their assistance with collecting samples, fellow scientists, Ker Sin Tan, Isabella Ciurej, Jyothsna Rao and Yih Rue Ong for their assistance with isolating and analysing the cells, Dr Miranda Davies-Tuck for statistical advice and Ms Katherine Wyatt (all employed by Hudson Institute of Medical Research). The authors would like to thank Dr Roni Ratner for identifying potential participants (employed by Monash Health). MDT is funded by the National Health and Medical Research Stillbirth Centre of Research Excellence. All consented to acknowledgement and none had anything to disclose.
Funding Information:
This work was supported by the Australian National Health and Medical Research Council (grant numbers 545992, 104229, 1173882), the Royal Australian and New Zealand College of Obstetrics and Gynaecology (RANZCOG) Ella Macknight Memorial Scholarship, an Australian Postgraduate Award and the Victorian Government's Operational Infrastructure Support Program. The authors would like to thank the Ritchie Centre Tissue Bank research nurses, Ms. Grace Heo, Erica O'Donoghue, Pam Mamers, Germana Ryan and Yao Han, for their assistance with collecting samples, fellow scientists, Ker Sin Tan, Isabella Ciurej, Jyothsna Rao and Yih Rue Ong for their assistance with isolating and analysing the cells, Dr Miranda Davies-Tuck for statistical advice and Ms Katherine Wyatt (all employed by Hudson Institute of Medical Research). The authors would like to thank Dr Roni Ratner for identifying potential participants (employed by Monash Health). MDT is funded by the National Health and Medical Research Stillbirth Centre of Research Excellence. All consented to acknowledgement and none had anything to disclose.
Publisher Copyright:
© 2021 Reproductive Healthcare Ltd.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - Research question: Are endometrial stem/progenitor cells shed into uterine menstrual blood (UMB) and the peritoneal cavity in women with and without endometriosis during menstruation? Design: Women with (n = 32) and without endometriosis (n = 29) at laparoscopy (total 61), carried out during the menstrual (n = 41) and non-menstrual phase (n = 20) were recruited. The UMB, peritoneal fluid and peripheral blood were analysed by clonogenicity assay and flow cytometry to quantify the concentrations of endometrial clonogenic cells, SUSD2+ mesenchymal stem cells (eMSC) and N-cadherin+ epithelial progenitor cells (eEPC). Results: Clonogenic endometrial cells, eMSC and eEPC were found in most UMB samples at similar concentrations in women with and without endometriosis. In contrast, 62.5% of women with endometriosis and 75.0% without (controls) had clonogenic cells in peritoneal fluid samples during menses. The eMSC were present in the peritoneal fluid of 76.9% of women with endometriosis and 44.4% without, and eEPC were found in the peritoneal fluid of 60.0% of women with and 25.0% without endometriosis during menses. Median clonogenic, eMSC and eEPC concentrations in peritoneal fluid were not significantly different between groups. More clonogenic cells persisted beyond the menstrual phase in the peritoneal fluid of women with endometriosis (menstrual 119/ml [0–1360/ml] versus non-menstrual 8.5/ml [0–387/ml]; P = 0.277) compared with controls (menstrual 76.5/ml [1–1378/ml] versus non-menstrual 0/ml [0–14/ml]; P = 0.0362). No clonogenic endometrial cells were found in peripheral blood. Conclusions: Clonogenic endometrial cells, SUSD2+ eMSC and N-cadherin+ eEPC are present in UMB and the peritoneal fluid of women with and without endometriosis. Further study of the function of these cells may shed light on the cellular origins of endometriosis.
AB - Research question: Are endometrial stem/progenitor cells shed into uterine menstrual blood (UMB) and the peritoneal cavity in women with and without endometriosis during menstruation? Design: Women with (n = 32) and without endometriosis (n = 29) at laparoscopy (total 61), carried out during the menstrual (n = 41) and non-menstrual phase (n = 20) were recruited. The UMB, peritoneal fluid and peripheral blood were analysed by clonogenicity assay and flow cytometry to quantify the concentrations of endometrial clonogenic cells, SUSD2+ mesenchymal stem cells (eMSC) and N-cadherin+ epithelial progenitor cells (eEPC). Results: Clonogenic endometrial cells, eMSC and eEPC were found in most UMB samples at similar concentrations in women with and without endometriosis. In contrast, 62.5% of women with endometriosis and 75.0% without (controls) had clonogenic cells in peritoneal fluid samples during menses. The eMSC were present in the peritoneal fluid of 76.9% of women with endometriosis and 44.4% without, and eEPC were found in the peritoneal fluid of 60.0% of women with and 25.0% without endometriosis during menses. Median clonogenic, eMSC and eEPC concentrations in peritoneal fluid were not significantly different between groups. More clonogenic cells persisted beyond the menstrual phase in the peritoneal fluid of women with endometriosis (menstrual 119/ml [0–1360/ml] versus non-menstrual 8.5/ml [0–387/ml]; P = 0.277) compared with controls (menstrual 76.5/ml [1–1378/ml] versus non-menstrual 0/ml [0–14/ml]; P = 0.0362). No clonogenic endometrial cells were found in peripheral blood. Conclusions: Clonogenic endometrial cells, SUSD2+ eMSC and N-cadherin+ eEPC are present in UMB and the peritoneal fluid of women with and without endometriosis. Further study of the function of these cells may shed light on the cellular origins of endometriosis.
KW - Endometrial stem/progenitor cells
KW - N-cadherin
KW - Peritoneal fluid
KW - Retrograde menstruation
KW - Sushi domain containing 2 (SUSD2)
UR - http://www.scopus.com/inward/record.url?scp=85106322265&partnerID=8YFLogxK
U2 - 10.1016/j.rbmo.2021.04.008
DO - 10.1016/j.rbmo.2021.04.008
M3 - Article
C2 - 34011465
AN - SCOPUS:85106322265
SN - 1472-6483
VL - 43
SP - 3
EP - 13
JO - Reproductive BioMedicine Online
JF - Reproductive BioMedicine Online
IS - 8
ER -