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Published on: August 3, 2017
Programmed cell death and clearance of cell corpses in Caenorhabditis elegans
Xiaochen Wang1, Chonglin Yang2
1National Institute of Biological Sciences, No. 7 Science Park Road, Zhongguancun Life Science Park, Beijing, 102206, China. wangxiaochen@nibs.ac.cn.
Abstract:
Programmed cell death is critical to the development of diverse animal species from C. elegans to humans. In C. elegans, the cell death program has three genetically distinguishable phases. During the cell suicide phase, the core cell death machinery is activated through a protein interaction cascade. This activates the caspase CED-3, which promotes numerous pro-apoptotic activities including DNA degradation and exposure of the phosphatidylserine "eat me" signal on the cell corpse surface. Specification of the cell death fate involves transcriptional activation of the cell death initiator EGL-1 or the caspase CED-3 by coordinated actions of specific transcription factors in distinct cell types. In the cell corpse clearance stage, recognition of cell corpses by phagocytes triggers several signaling pathways to induce phagocytosis of apoptotic cell corpses. Cell corpse-enclosing phagosomes ultimately fuse with lysosomes for digestion of phagosomal contents. This article summarizes our current knowledge about programmed cell death and clearance of cell corpses in C. elegans.
Insights
Programmed cell death in C. elegans involves distinct suicide and clearance phases. This process is crucial for development, involving specific genes like EGL-1 and caspase CED-3 for cell corpse removal.
Area of Science:
- Developmental Biology
- Cell Biology
- Genetics
Background:
- Programmed cell death is essential for animal development across species.
- The nematode C. elegans exhibits a well-characterized cell death program with distinct phases.
Purpose of the Study:
- To summarize current knowledge on programmed cell death (PCD) and cell corpse clearance in C. elegans.
- To detail the genetic and molecular mechanisms underlying these processes.
Main Methods:
- Review of existing literature on C. elegans programmed cell death.
- Analysis of genetic pathways involved in cell suicide and phagocytosis.
Main Results:
- C. elegans PCD occurs in three genetically defined phases: suicide, engulfment, and digestion.
- Key genes like EGL-1 and caspase CED-3 regulate apoptosis initiation and execution.
- Phagocytosis of cell corpses involves specific recognition and signaling pathways.
Conclusions:
- The C. elegans model provides fundamental insights into conserved mechanisms of programmed cell death and clearance.
- Understanding these processes is vital for comprehending development and disease in higher organisms.
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