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An Apoptotic 'Eat Me' Signal: Phosphatidylserine Exposure
Katsumori Segawa1, Shigekazu Nagata1
1Laboratory of Biochemistry and Immunology, WPI Immunology Frontier Research Center, Osaka University, 3-1 Yamada-oka, Suita 565-0871, Japan.
Abstract:
Apoptosis and the clearance of apoptotic cells are essential processes in animal development and homeostasis. For apoptotic cells to be cleared, they must display an 'eat me' signal, most likely phosphatidylserine (PtdSer) exposure, which prompts phagocytes to engulf the cells. PtdSer, which is recognized by several different systems, is normally confined to the cytoplasmic leaflet of the plasma membrane by a 'flippase'; apoptosis activates a 'scramblase' that quickly exposes PtdSer on the cell surface. The molecules that flip and scramble phospholipids at the plasma membrane have recently been identified. Here we discuss recent findings regarding the molecular mechanisms of apoptotic PtdSer exposure and the clearance of apoptotic cells.
Insights
Cellular
Area of Science:
- Cell Biology
- Biochemistry
Background:
- Apoptosis is crucial for development and homeostasis.
- Clearance of apoptotic cells requires 'eat me' signals, like phosphatidylserine (PtdSer) exposure.
- PtdSer is normally on the inner cell membrane but flips to the outer surface during apoptosis.
Purpose of the Study:
- To discuss recent findings on the molecular mechanisms of apoptotic PtdSer exposure.
- To review the mechanisms of apoptotic cell clearance.
Main Methods:
- Identification of phospholipid flippase and scramblase molecules.
- Discussion of molecular mechanisms regulating PtdSer exposure.
Main Results:
- The molecules responsible for phospholipid flipping and scrambling have been identified.
- Apoptosis triggers scramblase activation, leading to PtdSer externalization.
Conclusions:
- Understanding PtdSer exposure mechanisms is key to apoptotic cell clearance.
- Recent discoveries illuminate the molecular basis of PtdSer exposure and cell engulfment.
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