Equine cervical remodeling during placentitis and the prepartum period: a transcriptomic approach

Author:

El-Sheikh Ali Hossam12,Scoggin Kirsten E1,Ruby Rebecca3,Loynachan Alan3,Boakari Yatta4,Fernandes Claudia5,Dini Pouya6,Fedorka Carleigh Elizabeth1,Loux Shavahn C1,Esteller-Vico Alejandro7,Ball Barry A1

Affiliation:

1. 1Maxwell H. Gluck Equine Research Center, Department of Veterinary Science, University of Kentucky, Lexington, Kentucky, USA

2. 2Theriogenology Department, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt

3. 3UK Veterinary Diagnostic Laboratory, University of Kentucky, Kentucky, USA

4. 4Department of Clinical Sciences, Auburn University College of Veterinary Medicine, Auburn, Alabama, USA

5. 5Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil

6. 6Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, California, USA

7. 7Department of Biomedical and Diagnostic Sciences, University of Tennessee, Knoxville, Tennessee, USA

Abstract

Cervical remodeling is a critical component in both term and preterm labor in eutherian mammals. However, the molecular mechanisms underlying cervical remodeling remain poorly understood in the mare. The current study compared the transcriptome of the equine cervix (cervical mucosa (CM) and stroma (CS)) during placentitis (placentitis group, n  = 5) and normal prepartum mares (prepartum group, n  = 3) to normal pregnant mares (control group, n  = 4). Transcriptome analysis identified differentially expressed genes (DEGs) during placentitis (5310 in CM and 907 in CS) and during the normal prepartum period (189 in CM and 78 in CS). Our study revealed that cervical remodeling during placentitis was dominated by inflammatory signaling as reflected by the overrepresented toll-like receptor signaling, interleukin signaling, T cell activation, and B cell activation pathways. These pathways were accompanied by upregulation of several proteases, including matrix metalloproteinases (MMP1, MMP2, and MMP9), cathepsins (CTSB, CTSC, and CTSD) and a disintegrin and metalloproteinase with thrombospondin type 1 motifs (ADAMTS1, ADAMTS4, and ADAMTS5), which are crucial for degradation of cervical collagens during remodeling. Cervical remodeling during placentitis was also associated with upregulation of water channel-related transcripts (AQP9 and RLN), angiogenesis-related transcripts (NOS3, ENG1, THBS1, and RAC2), and aggrecan (ACAN), a hydrophilic glucosaminoglycan, with subsequent cervical hydration. The normal prepartum cervix was associated with upregulation of ADAMTS1, ADAMTS4, NOS3 and THBS1, which might reflect an early stage of cervical remodeling taking place in preparation for labor. In conclusion, our findings revealed the possible key regulators and mechanisms underlying equine cervical remodeling during placentitis and the normal prepartum period.

Publisher

Bioscientifica

Subject

Cell Biology,Obstetrics and Gynecology,Endocrinology,Embryology,Reproductive Medicine

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