Munoz-Maceda Ana, Camacho Eva Pericuesta, Priego-Gonzalez Andrea, Núñez-Puente Carolina, de Los Reyes Nuria Martínez, Cerdeira Joaquín, Sanchez-Rodriguez Ana, Ramos-Ibeas Priscila, Rizos Dimitrios, Gutiérrez-Adán Alfonso, Roldan Eduardo R S, Sánchez-Calabuig María Jesús
Department of Animal Medicine and Surgery, Faculty of Veterinary Medicine, Complutense University of Madrid, Spain.
Department of Animal Reproduction, National Institute for Agricultural and Food Research and Technology (INIA-CSIC), Madrid, Spain.
Theriogenology. 2025 Aug 19;249:117641. doi: 10.1016/j.theriogenology.2025.117641.
In vitro embryo production (IVP) in felid species faces difficulties derived from their conservation status, challenging reproductive traits and low success rates during in vitro maturation (IVM), fertilization (IVF) and culture (IVC). This study aimed to evaluate different IVC strategies for domestic cat IVP, as a model to improve assisted reproduction techniques (ARTs) in wild felids. Three IVC media were compared: (i) synthetic oviductal fluid (SOF) supplemented with fetal bovine serum ("FBS"); (ii): SOF supplemented first with bovine serum albumin (BSA), followed by FBS addition ("BSA-FBS"); and (iii): a commercial IVC human medium (IVC-CULT®) ("COM"). A total of 1064 in vitro matured cat oocytes were fertilized with frozen-thawed epididymal spermatozoa, and 813 presumptive zygotes were cultured in the three experimental groups. Expanded blastocysts (n = 108) were snap-frozen or fixed for differential cell count and quantitative analysis of pluripotency-related gene expression. One-way ANOVA was used to assess differences in IVP rates and blastocyst developmental parameters. No significant differences in cleavage or blastocyst rates were found among groups, nor in total blastomere count (P > 0.05). However, the FBS group showed higher SOX2 pluripotency marker expression compared to the other groups, while BSA-FBS exhibited a more balanced SOX2/OCT4 ratio, linked to blastocyst competence in other species. Furthermore, a tendency was found towards a lower proportion of cells in the inner cell mass (ICM) in the FBS group. Our results suggest that elevated SOX2 expression alone may not reflect improved developmental competence in the domestic cat blastocysts. Instead, early BSA supplementation followed by FBS might enhance ICM differentiation, benefiting first from BSA's fatty acids and later from FBS's antioxidants and growth factors. Lastly, the commercial medium yielded comparable embryonic developmental outcomes to BSA-FBS, offering a viable alternative. Thus, this research represents a contribution to the refinement of IVP protocols in the domestic cat, promoting standardization that could be adapted for wild feline conservation.
猫科动物的体外胚胎生产(IVP)面临诸多困难,这些困难源于它们的保护状况、具有挑战性的繁殖特性以及体外成熟(IVM)、受精(IVF)和培养(IVC)过程中的低成功率。本研究旨在评估家猫IVP的不同IVC策略,作为改进野生猫科动物辅助生殖技术(ARTs)的模型。比较了三种IVC培养基:(i)添加胎牛血清(“FBS”)的合成输卵管液(SOF);(ii)先添加牛血清白蛋白(BSA),然后添加FBS的SOF(“BSA-FBS”);(iii)一种商业化的IVC人类培养基(IVC-CULT®)(“COM”)。总共1064个体外成熟的猫卵母细胞用冻融附睾精子受精,813个推定受精卵在三个实验组中培养。扩张的囊胚(n = 108)被速冻或固定,用于差异细胞计数和多能性相关基因表达的定量分析。使用单因素方差分析来评估IVP率和囊胚发育参数的差异。各组之间在卵裂率或囊胚率上没有发现显著差异,在总卵裂球计数上也没有差异(P > 0.05)。然而,与其他组相比,FBS组显示出更高的SOX2多能性标记表达,而BSA-FBS表现出更平衡的SOX2/OCT4比率,这与其他物种的囊胚能力有关。此外,发现FBS组内细胞团(ICM)中的细胞比例有降低的趋势。我们的结果表明,单独升高的SOX2表达可能无法反映家猫囊胚发育能力的提高。相反,早期添加BSA后再添加FBS可能会增强ICM分化,首先受益于BSA的脂肪酸,随后受益于FBS的抗氧化剂和生长因子。最后,商业化培养基产生的胚胎发育结果与BSA-FBS相当,提供了一个可行的替代方案。因此,本研究为改进家猫的IVP方案做出了贡献,促进了可适用于野生猫科动物保护的标准化。