Inyawilert Wilasinee, Liu Che-Ming, Liao Yu-Jing, Jitjumnong Jakree, Amporn Chalothon, Tang Pin-Chi
Department of Agricultural Science, Faculty of Agriculture Natural Resources and Environment, Naresuan University, Phitsanulok, 65000, Thailand.
The center of Agricultural Biotechnology, Naresuan University, Phitsanulok, 65000, Thailand.
Vet Anim Sci. 2024 Nov 5;26:100406. doi: 10.1016/j.vas.2024.100406. eCollection 2024 Dec.
Precise pregnancy detection is critical for optimizing reproductive efficiency in animals. In mice, the conventional copulation plug method for pregnancy confirmation lacks reliability, particularly in inbred strains, with false-pregnancy rates exceeding 50 %. Here, to improve pregnancy detection efficiency in mice, we examined vaginal cell population changes using vaginal smear technique and analyzed MMP-9 expression in vaginal tract from day 0.5 to 6.5 of pregnancy. A total of forty-four female mice in the estrus stage were paired with sexually mature male mice for natural mating. The morning after mating was considered as embryonic day 0.5 (E0.5). Vaginal cytology was used to determine the vaginal cells of pregnant and non-pregnant mice from day 0.5 to 6.5. Furthermore, the protein and gene expression of MMP-9 were assessed through the utilization of immunohistochemistry and real-time PCR. Our findings reveal that pregnant mice display the higher number of leukocytes but the low number of nucleated/cornified epithelial cells in vagina compared to the non-pregnant counterparts. Furthermore, MMP-9 protein consistently presents in vaginal epithelial cells throughout the experimental period, with increased protein expression on day 4.5 of pregnancy followed by a decline on day 6.5 of pregnancy. This result is similar to MMP-9 gene expression, reaching the peak on day 5.5 of pregnancy. In conclusion, vaginal cytology proves effective for mouse pregnancy determination, while MMP-9 can serve as a potential biomarker for detecting pregnancy in mice.
精确的妊娠检测对于优化动物繁殖效率至关重要。在小鼠中,用于确认妊娠的传统交配栓方法缺乏可靠性,尤其是在近交系中,假孕率超过50%。在此,为了提高小鼠妊娠检测效率,我们使用阴道涂片技术检查阴道细胞群体变化,并分析妊娠第0.5天至6.5天阴道中基质金属蛋白酶-9(MMP-9)的表达。总共44只处于发情期的雌性小鼠与性成熟雄性小鼠配对进行自然交配。交配后的早晨被视为胚胎第0.5天(E0.5)。从第0.5天至6.5天,使用阴道细胞学方法确定妊娠和未妊娠小鼠的阴道细胞。此外,通过免疫组织化学和实时聚合酶链反应评估MMP-9的蛋白质和基因表达。我们的研究结果表明,与未妊娠小鼠相比,妊娠小鼠阴道中的白细胞数量较多,但有核/角质化上皮细胞数量较少。此外,在整个实验期间,MMP-9蛋白始终存在于阴道上皮细胞中,在妊娠第4.5天蛋白质表达增加,随后在妊娠第6.5天下降。这一结果与MMP-9基因表达相似,在妊娠第5.5天达到峰值。总之,阴道细胞学被证明对小鼠妊娠测定有效,而MMP-9可作为检测小鼠妊娠的潜在生物标志物。