Abstract

BackgroundThe aim of the present study was to evaluate CCL8 and CXCL10 expression and its regulatory mechanism in peripheral blood leukocytes (PBLs) at the time of maternal recognition in cows. Blood samples were collected on 14, 15, 16, 17 and 18 d after artificial insemination (AI). Based on the day of return of estrus, cows were divided into three groups, pregnant (n = 5), early embryonic mortality (EEM; n = 5) and late embryonic mortality (LEM; n = 5). The gene expression levels in PBLs were assessed with quantitative real-time reverse transcription PCR.ResultsThe expression of CCL8 and CXCL10 mRNA in PBLs gradually increased from 14 to 18 d of pregnant cows and significant differences were observed on 18 d (P < 0.05), whereas no significant changes were observed both in EEM and LEM cows. Interferon-stimulated protein 15 kDa (ISG15), myxovirus-resistance gene (MX) 1 and MX2 mRNA expression in PBLs increased from 14 to 18 d which was significant on 18 d of pregnant cows as well as in LEM cows (P < 0.05), but no changes were observed in EEM cows. To determine whether the expression of CCL8 and CXCL10 in PBLs was regulated by pregnancy-related substances or not, expression level was assessed after exposure to interferon-τ (IFNT) and CCL16. Monocytes, granulocytes and lymphocytes were obtained using density-gradient centrifugation and flow cytometry. The addition of IFNT (100 ng/mL) and CCL16 (100 ng/mL) to cultured PBLs increased the expression of CCL8 and CXCL10 mRNA (P < 0.05). The expression of ISG15, MX1 and MX2 mRNA in PBLs was also stimulated by IFNT and CCL16 (P < 0.05).ConclusionsThe expression of CCL8 and CXCL10 genes increased in PBLs during early pregnancy. Since IFNT stimulated CCL8 and CXCL10 expression in cultured PBLs, the increase of CCL8 and CXCL10 might be pregnancy-dependent events. The expression of both CCL8 and CXCL10 in PBLs was stimulated by CCL16 as well as IFNT, suggesting a chemokine interaction that at least includes CCL8, CXCL10 and CCL16, and may play a role in regulating maternal recognition in cows.

Highlights

  • The aim of the present study was to evaluate CCL8 and CXCL10 expression and its regulatory mechanism in peripheral blood leukocytes (PBLs) at the time of maternal recognition in cows

  • ISG15, MX1 and MX2 mRNA expression in PBLs was significantly higher on 18 d than 14 d of pregnant cows as well as in late embryonic mortality (LEM) cows (Figs. 3, 4, and 5; P < 0.05), but no changes were observed in early embryonic mortality (EEM) cows

  • The addition of IFNT and CCL16 stimulated CCL8, CXCL10, ISG15, MX1 and MX2 mRNA expression in Discussion This study demonstrated that the expression of CCL8 and CXCL10 genes in PBLs increased on 18 d in pregnant cows, whereas this up-regulation was not observed in non-pregnant cows

Read more

Summary

Introduction

The aim of the present study was to evaluate CCL8 and CXCL10 expression and its regulatory mechanism in peripheral blood leukocytes (PBLs) at the time of maternal recognition in cows. The ability to detect pregnancy early would help to shorten interbreeding intervals, since nonpregnant cows can be given an opportunity to synchronize their estrous cycle and be artificially inseminated prior to Recent studies have shown that interferon-τ (IFNT), which is a known key maternal recognition factor, Sakumoto et al Journal of Animal Science and Biotechnology (2018) 9:46 stimulates the expression of interferon-stimulated genes (ISGs), such as interferon-stimulated protein 15 kDa (ISG15), myxovirus-resistance (MX) proteins 1 and 2, and 2′-5′-oligoadenylate synthetase 1 (OAS1) in peripheral blood leukocytes (PBLs) in cows [8,9,10,11,12,13,14]. A combination of gene expression of ISGs in PBLs and color Doppler ultrasonography of the corpus luteum on 20 d after AI in beef cattle was used as a feasible method to diagnose pregnancy with high accuracy [14]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call