Evidence for coopetition at the maternal–fetal interface shaping placental invasion

J Junaid Afzal (Division of Cardiology, Department of Medicine, University of California) Y Yasir Suhail (Department of Biomedical Engineering, University of Connecticut Health) W Wenqiang Du (Department of Biomedical Engineering, University of Connecticut Health) Y Yamin Liu (Department of Biomedical Engineering, University of Connecticut Health) R Ramalakshmi Ramasamy (The Jackson Laboratory) Z Zukai Liu R Ruchi Goyal (Department of Biomedical Engineering, University of Connecticut Health) A Ashkan Novin (Department of Biomedical Engineering, University of Connecticut Health) S Sameera Suhail (Department of Biomedical Engineering, University of Connecticut Health) J Jamie Maziarz (Systems Biology Institute, Yale West Campus) K Khadija Wali (Department of Biomedical Engineering, University of Connecticut Health) P Paul Robson G Günter P. Wagner K Kshitiz (Department of Biomedical Engineering, University of Connecticut Health)

Abstract

Coopetition is a term from game theory that describes a mix of cooperative and competitive behavior. The maternal–fetal interface (MFI) among eutherian mammals presents close interaction of two distinct individuals. These interactions have resulted in a remarkable diversity in MFI structure, often interpreted as the outcome of maternal–fetal conflict. Nevertheless, the fetus and the mother share evolutionary interests since 50% of fetal genes are maternal. In hemochorial species, characterized by invasive placentation, endometrial stromal fibroblasts (ESFs) undergo decidualization to regulate embryo implantation. In great apes, hemochorial placentation is driven by highly invasive extravillous trophoblast cells (EVT). Here, using EVTs differentiated from trophoblast stem cells, term placenta, as well as HTR8/SVneo, we demonstrate that EVTs orchestrate a transformation of the maternal stroma, reducing its resistance to invasion acquired during decidualization. Through paracrine signals, in particular IL-11, trophoblasts transform decidual ESFs from a matrix-producing to a matrix-degrading state. Notably, noninvasive cytotrophoblast cells, do not transform decidual ESFs. We further provide evidence that maternal coadaptation is critical to EVT-induced decidual transformation. Decidual ESFs upregulate expression of Suppressor of Cytokine Signaling 3 in response to EVTs, rewiring downstream IL-11 signaling from JAK/STAT to AP-1 specific transcription. We conclude that the evolution of highly invasive placentation is the outcome of both the evolution of invasive EVTs, as well as the evolution of maternal traits, i.e., the switch from JAK/STAT to AP-1 signaling. We interpret this as evidence for co-opetition (cooperation among competitors).

Article Details

Volume / Issue Vol. 122, Issue 36
Published September 09, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

J

Junaid Afzal

Division of Cardiology, Department of Medicine, University of California

Y

Yasir Suhail

Department of Biomedical Engineering, University of Connecticut Health

W

Wenqiang Du

Department of Biomedical Engineering, University of Connecticut Health

Y

Yamin Liu

Department of Biomedical Engineering, University of Connecticut Health

R

Ramalakshmi Ramasamy

The Jackson Laboratory

Z

Zukai Liu

R

Ruchi Goyal

Department of Biomedical Engineering, University of Connecticut Health

A

Ashkan Novin

Department of Biomedical Engineering, University of Connecticut Health

S

Sameera Suhail

Department of Biomedical Engineering, University of Connecticut Health

J

Jamie Maziarz

Systems Biology Institute, Yale West Campus

K

Khadija Wali

Department of Biomedical Engineering, University of Connecticut Health

P

Paul Robson

G

Günter P. Wagner

K

Kshitiz

Department of Biomedical Engineering, University of Connecticut Health