1College of Veterinary Medicine, Gansu Agricultural
University, 730070, Lanzhou, Gansu, China; 2Gansu Key Laboratory of Animal Generational Physiology and
Reproductive Regulation, 730070, Lanzhou, Gansu, China;
3Department of Theriogenology, University of Agriculture,
Faisalabad, 38000, Pakistan. 4
Department of Clinical Veterinary Medicine, College of Veterinary
Medicine, Huazhong Agricultural University, 430070, Wuhan, Hubei,
China.
*Corresponding author:
maxf@gsau.edu.cn
Abstract
Low endometrial receptivity is the major cause of failure in embryonic
implantation and early pregnancy loss in dairy cows. During peri-implantation,
bovine endometrial luminal epithelial cells (bELECs) undergo plasma membrane
transformation (PMT), the molecular mechanisms of which remain elusive. In this
study, we investigated the molecular mechanisms underlying PMT and its role in
endometrial receptivity. Analysis of mRNA data from the Gene Expression Omnibus
(GEO) database revealed that PMT occurs during the peri-implantation period and
is closely associated with the establishment of endometrial receptivity.
Interferon-tau (IFN-τ), a pregnancy recognition signal, promoted PMT in bELECs
by regulating the dishevelled segment
polarity protein 3 (DVL3)/Ras-related
C3 botulinum toxin substrate 2 (RAC2) signaling pathway, thereby
enhancing endometrial receptivity. IFN-τ upregulated DVL3 and RAC2 expression,
facilitating their interaction, which disrupted intercellular connections and
enhanced the migration and motility of bELECs. Concurrently, RAC2 accelerated
filamentous actin polymerization, further driving PMT. This process increased
the expression of PMT and endometrial receptivity markers, suggesting that the
DVL3/RAC2 signaling axis, downstream of IFN-τ, could be a potential therapeutic
target for rescuing embryo implantation failure caused by abnormal endometrial
receptivity in dairy cows.
To Cite This Article:
Ma X, Bai Z, Liu T, Saqib U, Hu J and Deng G, 2026. Interferon-tau enhances
bovine endometrial receptivity through dvl3/rac2 signaling-driven plasma
membrane transformation during implantation.
Pak Vet J, 46(1): 21-36.
http://dx.doi.org/10.29261/pakvetj/2026.011