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Molecular tension authenticates apoptotic cells being phagocytosed.

Min, C.; Cho, H.; Yu, J.; Moon, B.; Jeon, J.; Shahdab, N.; Moon, H.; Yang, S.; Lee, J.; Jin, J.; Hong, M.; Chung, W.-j.; Park, J.; Lee, G.; Park, D.

2024-06-10 cell biology
10.1101/2024.06.10.598189 bioRxiv
Show abstract

Profound cytoskeletal reorganization and plasma membrane deformation in phagocytes is indispensable for phagocytosis of massive apoptotic cells, but whether these dynamics accompany a mechanical signal modulating signaling during efferocytosis remains largely unexplored. Here, we report that tension between phosphatidylserine (PS) and PS receptors (PSR) generated at the phagocytic synapse serves as a signal to determine whether PS-exposing cells should be phagocytosed. Mechanistically, increased membrane tension of phagocytes via Rac1-dependent actin polymerization and membrane stiffness of apoptotic cells caused tension between PS and PSRs, leading to phosphoinositide 3-kinase recruitment to PSRs, which resulted in Rac1 inactivation and myosin II phosphorylation required for phagocytic cup closure. Our observations imply that tension between PS and PSRs acts as a mechanical fail-safe to prevent removal of all PS-exposing cells for the integrity of efferocytosis. One-Sentence SummaryTension between phosphatidylserine and its receptors acts as a final decision-maker determining phagocytosis of apoptotic cells.

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