Saki Jasem, Sabaghan Mohamad, Arjmand Reza, Teimoori Ali, Rashno Mohammad, Saki Ghasem, Shojaee Saeedeh
Cellular and Molecular Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Parasitology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Iran J Basic Med Sci. 2020 Sep;23(9):1164-1171. doi: 10.22038/ijbms.2020.43535.10224.
The protozoan as an intracellular protozoan is widely prevalent in humans and animals. Infection generally occurs through consuming food contaminated with oocysts and tissue cysts from undercooked meat. The parasite is carried in sexual fluids like semen but there is little information about the effect of on the male reproductive system. In this study, we examined the effect of tachyzoites on apoptosis induction in type B spermatogonia (GC-1) cells.
Fresh tachyzoites taken of infected BALB/c mice, GC-1 spg cells were infected with increasing concentrations of tachyzoites of , then apoptotic cells were identified and quantified by flow cytometry. The genes associated with apoptosis were evaluated by RT2 Profiler PCR Array.
PCR array analysis of 84 apoptosis-related genes demonstrated that 12 genes were up-regulated at least 4-fold and that one gene was down-regulated at least 2-fold in the infection group compared with levels in the control group. The number of genes whose expression had increased during the period of infection with was significantly higher than those whose expressions had decreased (18 versus 1) and Tnfrsf11b had the highest rate of gene expression.
induce apoptosis of GC-1 spg cells. This effect shows a trend of concentration-dependent increase so that with an increase in the ratio of parasite burden to spermatogonial cells, in addition to an increase in the number of genes whose expression has changed, the fold of these changes has increased as well.
作为一种细胞内原生动物,该原生动物在人类和动物中广泛流行。感染通常通过食用受卵囊和未煮熟肉类中的组织囊肿污染的食物而发生。这种寄生虫存在于精液等性液中,但关于其对男性生殖系统影响的信息很少。在本研究中,我们检测了该弓形虫速殖子对B型精原细胞(GC-1)凋亡诱导的影响。
取感染的BALB/c小鼠的新鲜速殖子,用不同浓度的该弓形虫速殖子感染GC-1 spg细胞,然后通过流式细胞术鉴定和定量凋亡细胞。通过RT2 Profiler PCR Array评估与凋亡相关的基因。
对84个凋亡相关基因的PCR阵列分析表明,与对照组相比,该弓形虫感染组中有12个基因上调至少4倍,1个基因下调至少2倍。在该弓形虫感染期间表达增加的基因数量显著高于表达减少的基因数量(18个对1个),且Tnfrsf11b的基因表达率最高。
该弓形虫诱导GC-1 spg细胞凋亡。这种作用呈浓度依赖性增加趋势,即随着寄生虫负荷与精原细胞比例的增加,除了表达发生变化的基因数量增加外,这些变化的倍数也增加了。