OCT4 protein and gene expression analysis in the differentiation of spermatogonia stem cells into neurons by immunohistochemistry, immunocytochemistry, and bioinformatics analysis.
Danial Hashemi KaroiiHossein AziziPublished in: Stem cell reviews and reports (2023)
Our findings can help us better understand the process of differentiation of spermatogonia stem cells into neurons, and it can be effective in finding new and more efficient treatments for neurogenesis and repair of neurons. We examined the OCT4 expression during the differentiation of SSCs into neurons (involving four stages in the following order: SSCs in vivo and in-vitro, embryonic Stem Cell-like (ES-like), Embryonic Bodies (EBs), and finally Neurons) by Immunocytochemistry (ICC), Immunohistochemistry (IMH), and Fluidigm Real-Time polymerase chain reaction. In addition, we use some databases like STRING to predict protein-protein interaction and enrichment analysis. We evaluated the expression of OCT4 in this process, and we observed that it is expressed in SSCs, ES-like, and EBs during the differentiation of spermatogonia stem cells into adult neurons. We show that by adding RA to EBs, the expression of OCT4 is reduced and is not expressed in the neuron cells. We observed that the expression of OCT4 is linked and interacts with the differentiation of spermatogonia stem cells into neuron cells, and it has been shown to be biologically functional, like stem cell maintenance and somatic cell reprogramming.
Keyphrases
- stem cells
- poor prognosis
- spinal cord
- optical coherence tomography
- gene expression
- cell therapy
- protein protein
- binding protein
- diabetic retinopathy
- induced apoptosis
- cell cycle arrest
- small molecule
- dna methylation
- single cell
- spinal cord injury
- brain injury
- disease activity
- cell death
- mesenchymal stem cells
- idiopathic pulmonary fibrosis
- big data
- amino acid