Marques J C S, Maciel J P O, Denis-Robichaud J, Madureira A M L, Conceicao R S, Moore S, Conley A, Lima F, Bartolomeu C C, Gomes W A, Cerri R L A
Faculty of Land and Food Systems, University of British Columbia, Vancouver, V6T 1Z4 Canada.
Faculty of Land and Food Systems, University of British Columbia, Vancouver, V6T 1Z4 Canada; Faculty of Veterinary Medicine, Rural Federal University of Pernambuco, Recife, 52171-900 Brazil.
J Dairy Sci. 2025 Oct;108(10):11651-11671. doi: 10.3168/jds.2025-26521. Epub 2025 Aug 5.
This study aimed to evaluate if different concentrations of progesterone (P4) before estrus and different intensities of estrous expression affected endometrial gene expression in lactating Holstein cows. Animals were randomly assigned into 2 experimental groups: control P4 and low P4. Cows underwent a presynchronization protocol involving a GnRH injection and P4 implant, followed by a PGF injection and implant removal after 7 d, and a second GnRH injection 48 h later. The P4 treatment began 3 d after the second GnRH injection, with low P4 cows receiving 3 PGF injections (12 h apart), and control P4 cows receiving no PGF injections. Five days after the start of treatment, all cows underwent a hormonal protocol identical to the presynchronization, except an estradiol cypionate injection replaced the second GnRH, given 24 h after P4 implant removal. Low P4 cows received additional PGF injections at 24, 36, and 48 h after the start of this second protocol. Physical activity was monitored by an activity monitor, and the duration and intensity of estrus were measured. A total of 33 cows (control P4: n = 16; low P4: n = 17) were submitted to uterine biopsy 7 and 14 d after the identified estrous event. Total RNA was extracted from each sample, and the NanoString nCounter system (NanoString Technologies) was used to determine the abundance of specific mRNA molecules for 91 genes. In addition to the P4 treatment, cows were classified as high or low estrous expression based on the median estrous intensity and duration. Gene expression data were normalized and analyzed using a mixed linear regression model with cow as random intercept. Significance for differential expression was set at false discovery rate <0.1 and absolute fold change ≥1.5. The P4 treatment was not associated with changes in endometrial gene expression 7 d after estrus. However, at d 14, a total of 17 target gene transcripts were differentially expressed between the treatment groups. In low P4 cows, upregulated genes were related to the immune system (CXCL8, CCL22, IL1B, IL1A, PTX3) and extracellular matrix remodeling (MMP3, MMP9, MMP1), compared with control P4. Estrous expression alone did not affect gene expression. However, its interaction with the P4 treatment influenced several target genes, with most changes observed 14 d postestrus. Low P4 concentrations during the follicular growth in cows that had low intensity of estrus were linked to decreased endometrial expression of growth factors (IGF1, IGF2) and increased expression of genes related to the immune system (CCL22, CCL2, CCL4, MUC1, NFKB2, PTX3) and PGF synthesis (SLCO2A1, PTGES) 14 d after estrus compared control P4. Pathway analysis linked β-estradiol as a potential upstream regulator of the genes affected by the interaction between P4 and estrus. When estradiol concentrations near the onset of estrus were measured, we found that estradiol modulated endometrial expression of IGF1 and MUC1 genes, but this effect was observed only under the low P4 treatment. In conclusion, our study revealed substantial differences in endometrial gene expression between cows treated with different P4 concentrations during the follicular growth and expressing different intensities of estrus.
本研究旨在评估发情前不同浓度的孕酮(P4)以及不同强度的发情表现是否会影响泌乳期荷斯坦奶牛的子宫内膜基因表达。动物被随机分为2个实验组:对照P4组和低P4组。奶牛接受了一个预同步方案,包括一次GnRH注射和P4植入,7 d后进行一次PGF注射并取出植入物,48 h后进行第二次GnRH注射。P4处理在第二次GnRH注射后3 d开始,低P4组奶牛接受3次PGF注射(间隔12 h),对照P4组奶牛不接受PGF注射。处理开始5 d后,所有奶牛接受与预同步相同的激素方案,但在取出P4植入物24 h后,用环丙孕酮注射替代第二次GnRH。低P4组奶牛在第二个方案开始后24、36和48 h接受额外的PGF注射。通过活动监测器监测身体活动,并测量发情的持续时间和强度。在确定发情事件后的7 d和14 d,共33头奶牛(对照P4组:n = 16;低P4组:n = 17)接受了子宫活检。从每个样本中提取总RNA,并使用NanoString nCounter系统(NanoString Technologies)测定91个基因的特定mRNA分子丰度。除了P4处理外,根据发情强度和持续时间的中位数,奶牛被分为高发情表达或低发情表达。基因表达数据使用以奶牛为随机截距的混合线性回归模型进行归一化和分析。差异表达的显著性设定为错误发现率<0.1且绝对倍数变化≥1.5。P4处理与发情后7 d子宫内膜基因表达的变化无关。然而,在第14天,处理组之间共有17种靶基因转录本差异表达。与对照P4组相比,低P4组奶牛中上调的基因与免疫系统(CXCL8、CCL22、IL1B、IL1A、PTX3)和细胞外基质重塑(MMP3、MMP9、MMP1)有关。单独的发情表现不影响基因表达。然而,它与P4处理的相互作用影响了几个靶基因,大多数变化在发情后14 d观察到。发情强度低的奶牛在卵泡生长期间的低P4浓度与发情后14 d子宫内膜生长因子(IGF1、IGF2)表达降低以及与免疫系统(CCL22、CCL2、CCL4、MUC1、NFKB2、PTX3)和PGF合成(SLCO2A1、PTGES)相关的基因表达增加有关,与对照P4组相比。通路分析将β-雌二醇作为受P4和发情相互作用影响的基因的潜在上游调节因子。当测量发情开始时附近的雌二醇浓度时,我们发现雌二醇调节IGF1和MUC1基因的子宫内膜表达,但这种效应仅在低P4处理下观察到。总之,我们的研究揭示了在卵泡生长期间接受不同P4浓度处理且发情强度不同的奶牛之间,子宫内膜基因表达存在显著差异。