Retinoic acid and/or progesterone differentiate mouse induced pluripotent stem cells into male germ cells in vitro.
Javad Amini MahabadiAbolfazl Aazami TamehSayyed Alireza TalaeiMohammad KarimianTahereh RahiminiaSeyed Ehsan EnderamiSeyed Mohammad Gheibi HayatHossein NikzadPublished in: Journal of cellular biochemistry (2019)
Numerous reagents were employed for differentiating induced pluripotent stem cells (iPSCs) into male germ cells; however, the induction procedure was ineffective. The aim of this study was to improve the in vitro differentiation of mice iPSCs (miPSCs) into male germ cells with retinoic acid (RA) and progesterone (P). miPSCs were differentiated to embryoid bodies (EBs) in suspension with RA with or without progesterone for 0, 4, and 7 days. Then, the expression of certain genes at different stages of male germ cell development including Ddx4 (pre meiosis), Stra8 (meiosis), AKAP3 (post meiosis), and Mvh protein was examined in RNA and/or protein levels by real-time polymerase chain reaction or flow cytometry, respectively. The Stra8 gene expression increased in the RA groups on all days. But, expression of this gene declined in RA + P groups. In addition, an increased expression of Ddx4 gene was observed on day 0 in the P group. Also, a significant upregulation was observed in the expression of AKAP3 gene in the RA + P group on days 0 and 4. However, gene expression decreased in P and RA groups on day 7. The expression of Mvh protein significantly increased in the RA group on day 7. The Mvh expression was also enhanced in the P group on day 4, but it decreased on day 7, while this protein upregulated on day 0 and 7 in the RA + P group. The miPSCs have the capacity for in vitro differentiation into male germ cells by RA and/or progesterone. However, the effects of these inducers depend on the type of combination and an effective time.
Keyphrases
- poor prognosis
- rheumatoid arthritis
- gene expression
- induced apoptosis
- binding protein
- disease activity
- induced pluripotent stem cells
- cell cycle arrest
- ankylosing spondylitis
- long non coding rna
- genome wide
- flow cytometry
- signaling pathway
- systemic lupus erythematosus
- amino acid
- oxidative stress
- copy number
- cell death
- interstitial lung disease
- computed tomography
- genome wide identification
- minimally invasive
- metabolic syndrome
- magnetic resonance imaging
- transcription factor
- adipose tissue
- germ cell
- systemic sclerosis
- high fat diet induced