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Animal reproduction science2019; 210; 106192; doi: 10.1016/j.anireprosci.2019.106192

Cyclical cervical function in the mare involves remodelling of collagen content, which is correlated with modification of oestrogen receptor 1 abundance.

Abstract: This study was conducted to elucidate mare cervical dilation mechanisms by testing two hypotheses: (i) the proportion of collagen staining in histological samples of mare cervices and (ii) the abundance of hormone receptors in the equine cervix differ with stage of the oestrous cycle and site within the cervix. Tissues and jugular vein blood samples were collected from 15 mares. Collagen content was assessed using Masson's Trichome staining. Receptor abundance was assessed using RT-PCR, qRT-PCR and immunohistochemistry. In sub-epithelial stroma, there was less collagen during the follicular than luteal phase, in the caudal- (P =  0.029), mid- (P =  0.0000) and cranial (P =  0.001) cervical tissue. In the deep stroma, there was less collagen staining during the follicular stage in the mid- (P =  0.004) and cranial- (P =  0.041) cervical regions. There were PTGER2, PTGER3, PGR and ESR1 mRNA transcripts in the cervix. A greater proportion of cells were positive for ESR1 protein during the follicular phase in sub-epithelial (P =  0.019) and deep (P =  0.013) stroma. The abundance of ESR1 in the epithelium was negatively correlated with collagen staining in sub-epithelial (P =  0.007) and deep (P =  0.005) stroma. The results of the study provide new information about the cervical biology of mares by increasing the knowledge about collagen content and the relationship between collagen content and ESR1 protein abundance during the oestrous cycle which indicates the ESR1 receptor is a candidate for involvement in control of cervical dilation.
Publication Date: 2019-09-12 PubMed ID: 31635778DOI: 10.1016/j.anireprosci.2019.106192Google Scholar: Lookup
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  • Journal Article

Summary

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The study investigates how collagen content and hormone receptor abundance in mares’ cervices vary through different stages of the oestrous cycle, as these may play a significant role in the mechanism of cervical dilation.

Objective of the Research

  • The study aimed to shed light on the mechanisms of cervical dilation in mares. Two primary hypotheses were tested: one related to the variance in collagen content in histological samples of the mares’ cervices, and the other regarding the change in hormone receptor abundance in the equine cervix with the stage of the oestrous cycle and site within the cervix.

Methodology

  • Researchers collected tissue samples and jugular vein blood samples from 15 different mares.
  • The Masson’s Trichome staining method was used to assess the collagen content.
  • The abundance of hormone receptors was evaluated using techniques such as RT-PCR, qRT-PCR, and immunohistochemistry.

Findings

  • It was discovered that in the sub-epithelial stroma, less collagen was observed during the follicular phase than the luteal phase, irrespective of the part of the cervix (caudal, mid, or cranial).
  • Similarly, in the deep stroma, there was lesser collagen staining during the follicular stage in the mid and cranial cervical regions.
  • Molecular analyses revealed the presence of PTGER2, PTGER3, PGR, and ESR1 mRNA transcripts in the cervix.
  • A higher proportion of cells were found to be positive for the ESR1 protein during the follicular phase in both the sub-epithelial and the deep stroma.
  • A negative correlation was observed between ESR1 abundance in the epithelium and collagen staining in the sub-epithelial and deep stroma.

Significance of the Research

  • The findings present new information about mare cervical biology, enhancing understanding of collagen content’s changes and its relationship with ESR1 protein abundance during the oestrous cycle.
  • The study suggests the ESR1 receptor as a potential player in controlling cervical dilation. More in-depth research in this direction could lead to new interventions and treatments related to equine reproductive health.

Cite This Article

APA
Campbell MLH, Peachey L, Callan L, Wathes DC, de Mestre AM. (2019). Cyclical cervical function in the mare involves remodelling of collagen content, which is correlated with modification of oestrogen receptor 1 abundance. Anim Reprod Sci, 210, 106192. https://doi.org/10.1016/j.anireprosci.2019.106192

Publication

ISSN: 1873-2232
NlmUniqueID: 7807205
Country: Netherlands
Language: English
Volume: 210
Pages: 106192
PII: S0378-4320(19)30121-6

Researcher Affiliations

Campbell, M L H
  • The Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL9 7TA, UK; Department of Pathobiology and Population Sciences, UK. Electronic address: mcampbell@rvc.ac.uk.
Peachey, L
  • The Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL9 7TA, UK.
Callan, L
  • The Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL9 7TA, UK.
Wathes, D C
  • The Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL9 7TA, UK; Department of Pathobiology and Population Sciences, UK.
de Mestre, A M
  • The Royal Veterinary College, Hawkshead Lane, North Mymms, Herts, AL9 7TA, UK; Department of Comparative Biomedical Sciences, UK.

MeSH Terms

  • Animals
  • Cervix Uteri / physiology
  • Cloning, Molecular
  • Collagen / physiology
  • DNA, Complementary / genetics
  • DNA, Complementary / metabolism
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / metabolism
  • Estrogen Receptor beta / genetics
  • Estrogen Receptor beta / metabolism
  • Estrous Cycle / physiology
  • Female
  • Gene Expression Regulation / physiology
  • Horses
  • Labor Stage, First / physiology
  • Luteinizing Hormone / genetics
  • Luteinizing Hormone / metabolism
  • Pregnancy
  • Progesterone / metabolism
  • RNA / genetics
  • RNA / metabolism
  • Receptors, FSH / genetics
  • Receptors, FSH / metabolism
  • Receptors, Prostaglandin E, EP2 Subtype / genetics
  • Receptors, Prostaglandin E, EP2 Subtype / metabolism
  • Receptors, Prostaglandin E, EP3 Subtype / genetics
  • Receptors, Prostaglandin E, EP3 Subtype / metabolism

Citations

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