Jharna Jannatul Ferdous, Bari Md Wasim, Alfian Norermi Firzana, Kishigami Satoshi
Department of Integrated Applied Life Science, Integrated Graduate School of Medicine, Engineering, and Agricultural Sciences, University of Yamanashi, Yamanashi 400-8510, Japan.
Faculty of Life and Environmental Sciences, University of Yamanashi, Yamanashi 400-8510, Japan.
Int J Mol Sci. 2025 Jul 21;26(14):6989. doi: 10.3390/ijms26146989.
Bovine serum albumin (BSA), the most commonly used protein in preimplantation embryo culture media, performs a variety of physiological functions. However, its involvement in long-term effects remains largely unclear. To investigate its physiological importance in culture media, we examined the developmental and metabolic consequences of BSA deprivation during preimplantation stages in mice. Embryos cultured in BSA-free media during specific time windows exhibited impaired blastocyst formation, with continuous deprivation from the two-pronuclei (2PN) stage significantly reducing trophectoderm (TE) and inner cell mass (ICM) cell numbers ( < 0.05), indicating compromised viability. Short-term BSA deprivation similarly disrupted lineage allocation, underscoring the sensitivity of early embryos to nutrient availability during cell fate determination. Although birth rates remained unaffected, suggesting compensatory mechanisms, longitudinal analysis revealed sex-specific metabolic dysfunction. Male offspring developed progressive glucose intolerance by 16 weeks, exhibiting elevated fasting glucose levels ( < 0.05) and impaired glucose clearance, whereas females showed no significant alterations in glucose metabolism. This study demonstrates that protein restriction during the preimplantation period not only disrupts early embryonic development but also programs long-term metabolic dysfunction, underscoring the importance of optimizing culture conditions in assisted reproductive technologies to minimize future health risks.
牛血清白蛋白(BSA)是植入前胚胎培养基中最常用的蛋白质,具有多种生理功能。然而,其在长期影响中的作用仍 largely 不清楚。为了研究其在培养基中的生理重要性,我们检查了小鼠植入前阶段 BSA 缺乏的发育和代谢后果。在特定时间窗口内在无 BSA 培养基中培养的胚胎表现出囊胚形成受损,从双原核(2PN)阶段开始持续缺乏显著减少滋养外胚层(TE)和内细胞团(ICM)细胞数量(<0.05),表明活力受损。短期 BSA 缺乏同样扰乱了谱系分配,强调了早期胚胎在细胞命运决定过程中对营养可用性的敏感性。尽管出生率未受影响,表明存在补偿机制,但纵向分析揭示了性别特异性的代谢功能障碍。雄性后代到 16 周时出现进行性葡萄糖不耐受,空腹血糖水平升高(<0.05)且葡萄糖清除受损,而雌性在葡萄糖代谢方面无显著变化。这项研究表明,植入前阶段的蛋白质限制不仅会破坏早期胚胎发育,还会导致长期的代谢功能障碍,强调了在辅助生殖技术中优化培养条件以最小化未来健康风险的重要性。