Department of Microbiology, Immunology and Molecular Genetics, University of Kentucky College of Medicine, Lexington, KY 40526, USA.
Trends Parasitol. 2012 Sep;28(9):358-64. doi: 10.1016/j.pt.2012.06.006. Epub 2012 Jul 18.
Programmed cell death (PCD) pathways remain understudied in parasitic protozoa in spite of the fact that they provide potential targets for the development of new therapy. The best understood PCD pathway in higher eukaryotes is apoptosis although emerging evidence also points to autophagy as a mediator of death in certain physiological contexts. Bioinformatic analyses coupled with biochemical and cell biological studies suggest that parasitic protozoa possess the capacity for PCD including a primordial form of apoptosis. Recent work in Toxoplasma and emerging data from Plasmodium suggest that autophagy-related processes may serve as an additional death promoting pathway in Apicomplexa. Detailed mechanistic studies into the molecular basis for PCD in parasitic protozoa represent a fertile area for investigation and drug development.
尽管程序性细胞死亡 (PCD) 途径为开发新疗法提供了潜在靶点,但在寄生原生动物中仍研究不足。在高等真核生物中,研究最为透彻的 PCD 途径是细胞凋亡,尽管新出现的证据也表明自噬在某些生理情况下是死亡的介导者。生物信息学分析结合生化和细胞生物学研究表明,寄生原生动物具有 PCD 的能力,包括原始形式的细胞凋亡。最近在弓形虫中的研究工作和来自疟原虫的新兴数据表明,与自噬相关的过程可能在顶复门中作为另一种促进死亡的途径。寄生原生动物中 PCD 的分子基础的详细机制研究代表了一个富有成效的研究和药物开发领域。