Porcine Germ Cells Phenotype during Embryonic and Adult Development.
Amanda Soares JorgeKaiana RecchiaMayra Hirakawa GlóriaAline Fernanda de SouzaLaís Vicari de Figueirêdo PessôaPaulo Fantinato NetoDaniele Dos Santos MartinsAndré Furugen Cesar de AndradeSimone Maria Massami Kitamura MartinsFabiana Fernandes BressanNaira Caroline Godoy PieriPublished in: Animals : an open access journal from MDPI (2023)
Primordial germ cells (PGCs) are the precursors of gametes. Due to their importance for the formation and reproduction of an organism, understanding the mechanisms and pathways of PGCs and the differences between males and females is essential. However, there is little research in domestic animals, e.g., swine, regarding the epigenetic and pluripotency profiles of PGCs during development. This study analyzed the expression of epigenetic and various pluripotent and germline markers associated with the development and differentiation of PGCs in porcine (pPGCs), aiming to understand the different gene expression profiles between the genders. The analysis of gonads at different gestational periods (from 24 to 35 days post fertilization (dpf) and in adults) was evaluated by immunofluorescence and RT-qPCR and showed phenotypic differences between the gonads of male and female embryos. In addition, the pPGCs were positive for OCT4 and VASA; some cells were H3k27me3 positive in male embryos and adult testes. In adults, the cells of the testes were positive for germline markers, as confirmed by gene expression analysis. The results may contribute to understanding the pPGC pathways during reproductive development, while also contributing to the knowledge needed to generate mature gametes in vitro.
Keyphrases
- induced apoptosis
- cell cycle arrest
- endoplasmic reticulum stress
- dna methylation
- gene expression
- pregnant women
- cell death
- oxidative stress
- signaling pathway
- cell proliferation
- weight gain
- dna damage
- optical coherence tomography
- binding protein
- physical activity
- weight loss
- genome wide identification
- transcription factor
- cell fate