bioRxiv Science⌕ Search

Biology subjects

Palomares, A. R.

Publications and source records attributed to Palomares, A. R..

2 recordsLinked to original sources

Vitrification-warming delays preimplantation development and impairs mitochondrial function and cytoplasmic lattices integrity in mouse embryos

Vitrification and warming of human embryos have become standardized procedures in assisted reproduction over the past two decades. Although generally considered safe, their full impact on embryo development remains unclear. Epidemiological studies have raised concerns about differences in birth weight and long-term health outcomes between newborns resulting from fresh versus frozen embryo transfers. In this study, we used mouse embryos to investigate the impact of vitrification and warming on developmental kinetics, mitochondrial function, and cytoplasmic lattice integrity. Time-lapse imaging revealed significant developmental delays across all preimplantation stages in vitrified embryos. Additionally, mitochondrial distribution, volume, and membrane potential exhibited signs of impairment. Ultrastructural analysis identified damage such as ruptured mitochondrial membranes, disrupted cytoplasmic lattices during early cell divisions, and underdeveloped mitochondrial cristae at the blastocyst stage. We hypothesize embryo vitrification and warming disrupt mitochondrial function and destabilize cytoplasmic lattice integrity, ultimately contributing to developmental delays in preimplantation embryos.

cell biology↗

Appropriate glycemic management protects the germline but not uterine environment in type 1 diabetes

Emerging evidence indicates that parental diseases can impact the health of subsequent generations through epigenetic inheritance. Recently, it was shown that maternal diabetes alters the metaphase II oocyte transcriptome, causing metabolic dysfunction in offspring. However, the type 1 diabetes (T1D) mouse models frequently utilized in previous studies may be subject to several confounding factors as a result of severe hyperglycemia. This limits clinical translatability due to improvements in glycemic control for T1D subjects. Therefore, we optimized a T1D mouse model to investigate the effects of appropriately managed maternal glycemic levels on oocytes and intrauterine development. We show that diabetic mice with appropriate glycemic control exhibited better long-term health outcomes, which maintains the oocyte transcriptome and chromatin accessibility. Moreover, we find that human oocytes undergoing in vitro maturation challenged with mildly increased levels of glucose, reflecting appropriate glycemic management, also retained their transcriptome. However, the fetal growth and placental function were still affected despite appropriate glycemic control, underscoring the uterine environment rather than the germline as a pathological factor for developmental programming in appropriately managed diabetes.

developmental biology↗