Autophagy-related gene and protein expressions during blastocyst development

Purpose This study aims to examine the expression of autophagic genes and proteins during blastocyst development and differentiation. Methods This is a prospective cohort study. Between March 2018 and November 2019, 30 females aged 30.13 +/- 4.83 years underwent an intracytoplasmic sperm injection (ICSI) cycle at Madina Fertility Center. ICSI was used to develop and incubate 82 leftover embryos to day 5. Then, the embryos were divided into two groups based on their developmental structure: group D (n = 49) included embryos that developed into blastocysts, whereas group A (n = 33) included arrested embryos. These embryos were used to investigate the autophagic gene and protein expressions. The current study was approved by the Clinical Trial Ethical Committee of the Faculty of Medicine, Alexandria University, following the ethical standards of scientific research (Registration no. 0303721). Results Embryos that developed into blastocysts on day 5 (group D) had significantly higher relative expression of the LC3 gene (1.11 +/- 0.52) and beclin-1 gene (1.43 +/- 0.34) and beclin-1 protein expression (3.8 +/- 0.028) than those that did not develop into blastocysts on day 5 (group A) [0.72 +/- 0.18 (P = 0.03), 0.35 +/- 0.12 (P = 0.0001), and 3.14 +/- 0.05, (P = 0.0001), respectively]. In contrast, mTOR and PIK3C3 protein expression was significantly higher in group A (arrested embryos) than those in group D (developed embryos) (P = 0.007 and P = 0.0001, respectively). Furthermore, the expression of the eIF4E gene was significantly lower in group D embryos (0.32 +/- 0.07) than that in group A embryos (4.38 +/- 1.16) (P = 0.0001). Conclusions This work identifies autophagy as a well regulated process required to maintain cell allocation and differentiation during late preimplantation embryo developmental stages.