Debrabant Alain, Lee Nancy, Bertholet Sylvie, Duncan Robert, Nakhasi Hira L
Laboratory of Bacterial, Parasitic and Unconventional Agents, Division of Emerging and Transfusion Transmitted Diseases, OBRR, CBER, US FDA, Bethesda, MD 20892, USA.
Int J Parasitol. 2003 Mar;33(3):257-67. doi: 10.1016/s0020-7519(03)00008-0.
In multicellular organisms, cellular growth and development can be controlled by programmed cell death (PCD), which is defined by a sequence of regulated events. However, PCD is thought to have evolved not only to regulate growth and development in multicellular organisms but also to have a functional role in the biology of unicellular organisms. In protozoan parasites and in other unicellular organisms, features of PCD similar to those in multicellular organisms have been reported, suggesting some commonality in the PCD pathway between unicellular and multicellular organisms. However, more extensive studies are needed to fully characterise the PCD pathway and to define the factors that control PCD in the unicellular organisms. The understanding of the PCD pathway in unicellular organisms could delineate the evolutionary origin of this pathway. Further characterisation of the PCD pathway in the unicellular parasites could provide information regarding their pathogenesis, which could be exploited to target new drugs to limit their growth and treat the disease they cause.
在多细胞生物中,细胞生长和发育可由程序性细胞死亡(PCD)控制,程序性细胞死亡由一系列受调控的事件定义。然而,人们认为程序性细胞死亡不仅进化而来以调控多细胞生物的生长和发育,而且在单细胞生物的生物学中也具有功能性作用。在原生动物寄生虫和其他单细胞生物中,已报道了与多细胞生物中类似的程序性细胞死亡特征,这表明单细胞生物和多细胞生物的程序性细胞死亡途径存在一些共性。然而,需要更广泛的研究来全面表征程序性细胞死亡途径,并确定控制单细胞生物中程序性细胞死亡的因素。对单细胞生物中程序性细胞死亡途径的理解可以描绘出该途径的进化起源。对单细胞寄生虫中程序性细胞死亡途径的进一步表征可以提供有关其发病机制的信息,这可用于开发新药物以限制其生长并治疗它们所引起的疾病。