Vohra H, Mahajan R C, Ganguly N K
Department of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Parasitol Res. 1998 Oct;84(10):835-8. doi: 10.1007/s004360050496.
To identify stage-specific molecules that might be important in pathogenicity, we focused on synchronizing Entamoeba histolytica HM1:1MSS axenic cultures by serum deprivation. By growing trophozoites in medium containing 2% serum for 16 h and then replacing with complete medium, we found that most of the trophozoites were in the G0/G1 phase of the cell cycle. Subsequently, the distribution of trophozoites in G0/G1, S and G2/M phases was studied for up to 24 h and it was observed that after 8 h, the trophozoites began to come out of the quiescent G0/G1 phase and the S and G2/M populations increased, indicating that certain serum factors regulate induction of cell division. It will be important to investigate these factors to find serum substitutes for cultivation media.
为了鉴定可能在致病性方面起重要作用的阶段特异性分子,我们专注于通过血清剥夺使溶组织内阿米巴HM1:1MSS无菌培养物同步化。通过在含有2%血清的培养基中培养滋养体16小时,然后换成完全培养基,我们发现大多数滋养体处于细胞周期的G0/G1期。随后,研究了滋养体在G0/G1、S和G2/M期的分布长达24小时,观察到8小时后,滋养体开始从静止的G0/G1期出来,S期和G2/M期群体增加,表明某些血清因子调节细胞分裂的诱导。研究这些因子以找到培养基的血清替代品将很重要。