Reproduction (Cambridge, England) · 2026
Evidence that heat shock protein A5 (HSPA5) plays a role during bovine in vitro embryo production.
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Santos Priscila Helena, Franchi Fernanda Fagali, Nunes Sarah Gomes, Fontes Patrícia Kubo, Manssur Thainá Sallum Bacco, Quaglio Ana Elisa Valencise, Nogueira Marcelo Fábio Gouveia, Castilho Anthony César de Souza
Аннотация
In brief: Heat shock protein A5 (HSPA5) is a protein involved in cellular protection and stress regulation, and is present in oviductal fluid; however, its role in bovine in-vitro embryo production remains unclear. This study demonstrates that rHSPA5 enhances oocyte mitochondrial activity and modulates gene expression related to embryonic development, thereby improving blastocyst formation rates. Abstract: Oviductal fluid (OF) proteins, such as heat shock protein A5 (HSPA5), play essential roles in reproductive physiology, including zona pellucida (ZP)-sperm interactions. Hypothesizing that HSPA5 interacts with oocytes, we evaluated its effects during the last 4 hr of bovine in-vitro cumulus-oocyte complex (COC) maturation and subsequent embryo development. The COCs were aspirated from slaughterhouse-derived cow ovaries and matured for 20 hr in base medium (BM). The medium was then partially replaced with BM (control) or BM supplemented with recombinant HSPA5 (100 ng/ml) for the final 4 hr of maturation. After maturation, COCs were either denuded for analysis or used for in-vitro fertilization and culture to assess embryo development to the blastocyst stage. To investigate HSPA5's role, we assessed the mitochondrial membrane potential, reactive oxygen species, and glutathione content in COCs and maturation medium, ZP solubility, oocyte penetration, blastocyst rates, and gene expression. Recombinant HSPA5 (rHSPA5) enhanced oocyte mitochondrial activity (p = 0.0006) and significantly increased the blastocyst yield (p = 0.04). Blastocysts from rHSPA5-treated oocytes showed upregulation of 19 genes associated with embryo quality, DNA methylation, cell growth, development, and oxidative stress. Although rHSPA5 did not alter the monospermic fertilization rate or oxidative stress in oocytes, it improved mitochondrial function, supported blastocyst development, and modulated embryonic transcriptional profiles. These findings suggest that rHSPA5 plays a beneficial role during the final phase of oocyte maturation, contributing to improved embryo quality and developmental competence in vitro.