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Actin dynamics and myosin contractility during plasma membrane repair and restoration: Does one ring really heal them
Eric Boucher1, Laurence Goldin-Blais1, Quentin Basiren1
1Department of Anatomy and Cell Biology, Faculty of Medicine, McGill University, Montreal, QC, Canada.
Abstract:
In order to survive daily insults, cells have evolved various mechanisms that detect, stabilize and repair damages done to their plasma membrane and cytoskeletal structures. Damage to the PM endangers wounded cells by exposing them to uncontrolled exchanges with the extracellular milieu. The processes and molecular machinery enabling PM repair are therefore at the center of the bulk of the investigations into single-cell repair program. Wounds are repaired by dynamically remodeling the composition and shape of the injured area through exocytosis-mediated release of intracellular membrane components to the wounded area, endocytosis-mediated removal of the injured area, or the shedding of the injury. The wound healing program of Xenopus oocytes and early Drosophila embryos is by contrast, mostly characterized by the rapid formation of a large membrane patch over the wound that eventually fuse with the plasma membrane which restores plasma membrane continuity and lead to the shedding of patch material into the extracellular space. Formation and contraction of actomyosin ring restores normal plasma membrane composition and organizes cytoskeletal repairs. The extend of the contributions of the cytoskeleton to the wound healing program of somatic cells have comparatively received little attention. This review offers a survey of the current knowledge on how actin dynamics, myosin-based contraction and other cytoskeletal structures affects PM and cortical cytoskeleton repair of somatic cells.
Insights
Cells repair plasma membrane (PM) damage using various mechanisms. This review focuses on how cytoskeletal structures, like actin and myosin, contribute to somatic cell repair, an area needing more research.
Area of Science:
- Cell biology
- Biochemistry
- Molecular biology
Background:
- Cells possess mechanisms to detect, stabilize, and repair damage to their plasma membrane (PM) and cytoskeletal structures.
- PM damage poses a risk to cells by allowing uncontrolled exchange with the extracellular environment.
- Investigating single-cell repair programs is crucial for understanding cellular survival.
Purpose of the Study:
- To review current knowledge on the role of cytoskeletal structures in plasma membrane and cortical cytoskeleton repair in somatic cells.
- To highlight the understudied contributions of the cytoskeleton to cellular wound healing.
- To survey how actin dynamics and myosin-based contraction influence cellular repair processes.
Main Methods:
- Literature review of existing research on cellular repair mechanisms.
- Analysis of studies focusing on plasma membrane repair and cytoskeletal involvement.
- Synthesis of findings related to actin dynamics, myosin contraction, and cytoskeletal structures in somatic cell repair.
Main Results:
- Cellular repair involves dynamic remodeling of the injured area via exocytosis, endocytosis, or shedding.
- Xenopus oocytes and Drosophila embryos exhibit rapid membrane patch formation for wound repair.
- Actomyosin ring formation and contraction are key for restoring PM composition and cytoskeletal integrity.
- The role of the cytoskeleton in somatic cell wound healing has received limited research attention.
Conclusions:
- Cytoskeletal elements, particularly actin dynamics and myosin-based contraction, play a significant role in somatic cell plasma membrane and cortical cytoskeleton repair.
- Further research is needed to fully elucidate the contributions of the cytoskeleton to the wound healing program in somatic cells.
- Understanding these mechanisms is vital for comprehending cellular resilience and repair processes.
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