TY - JOUR
T1 - Transcriptional Changes in Cumulus Cells During In Vitro Maturation of Human Oocytes
AU - Cadenas, Jesús
AU - Adrados, Cristina Subiran
AU - Kristensen, Stine Gry
AU - Macklon, Kirsten Tryde
AU - Greve, Vinnie Hornshøj
AU - Fedder, Jens
AU - Mamsen, Linn Salto
AU - Andersen, Claus Yding
N1 - © 2025 The Author(s). Molecular Reproduction and Development published by Wiley Periodicals LLC.
PY - 2025/6
Y1 - 2025/6
N2 - This study assessed transcriptional changes in human cumulus cells (CCs) during oocyte maturation In Vitro. CCs were collected from 25 cumulus-oocyte complexes derived from surplus ovarian medulla tissue of eight women (mean age 29 years, range 19-36) undergoing ovarian tissue cryopreservation without ovarian stimulation. Samples included CCs from fresh germinal vesicle (GV) oocytes (n = 5), and from GV (n = 8) and metaphase II (MII) oocytes (n = 12) after 48 h of In Vitro maturation (IVM). Microarray analysis revealed active signaling pathways during IVM, emphasizing LHCGR upregulation as central to oocyte maturation. Enhanced pathways included the insulin-like growth factor (IGF) system, particularly IGF2, and activin/inhibin signaling, while others appeared less active In Vitro compared to In Vivo. Differential expression analysis identified 1763 significantly expressed genes (DEGs) between fresh GV and MII-IVM, 50 DEGs between GV-IVM and MII-IVM, and 339 novel or unknown transcripts. Clustering highlighted additional pathways, such as MAPK, PPAR, Wnt, cholesterol metabolism, PI3K-AKT, TGF-β, focal adhesion, actin cytoskeleton regulation, and RANK/RANKL, with differential regulation during IVM. These findings underscore the complexity of signaling in CCs and the distinct regulatory mechanisms of human oocyte maturation In Vitro compared to In Vivo.
AB - This study assessed transcriptional changes in human cumulus cells (CCs) during oocyte maturation In Vitro. CCs were collected from 25 cumulus-oocyte complexes derived from surplus ovarian medulla tissue of eight women (mean age 29 years, range 19-36) undergoing ovarian tissue cryopreservation without ovarian stimulation. Samples included CCs from fresh germinal vesicle (GV) oocytes (n = 5), and from GV (n = 8) and metaphase II (MII) oocytes (n = 12) after 48 h of In Vitro maturation (IVM). Microarray analysis revealed active signaling pathways during IVM, emphasizing LHCGR upregulation as central to oocyte maturation. Enhanced pathways included the insulin-like growth factor (IGF) system, particularly IGF2, and activin/inhibin signaling, while others appeared less active In Vitro compared to In Vivo. Differential expression analysis identified 1763 significantly expressed genes (DEGs) between fresh GV and MII-IVM, 50 DEGs between GV-IVM and MII-IVM, and 339 novel or unknown transcripts. Clustering highlighted additional pathways, such as MAPK, PPAR, Wnt, cholesterol metabolism, PI3K-AKT, TGF-β, focal adhesion, actin cytoskeleton regulation, and RANK/RANKL, with differential regulation during IVM. These findings underscore the complexity of signaling in CCs and the distinct regulatory mechanisms of human oocyte maturation In Vitro compared to In Vivo.
KW - Humans
KW - Cumulus Cells/metabolism
KW - Female
KW - Oocytes/metabolism
KW - Adult
KW - In Vitro Oocyte Maturation Techniques
KW - Signal Transduction/physiology
KW - Transcription, Genetic/physiology
KW - Young Adult
KW - Gene Expression Profiling
UR - http://www.scopus.com/inward/record.url?scp=105008448642&partnerID=8YFLogxK
U2 - 10.1002/mrd.70035
DO - 10.1002/mrd.70035
M3 - Journal article
C2 - 40524476
SN - 1040-452X
VL - 92
SP - e70035
JO - Molecular Reproduction and Development
JF - Molecular Reproduction and Development
IS - 6
M1 - e70035
ER -