Squeezing in a Meal: Myosin Functions in Phagocytosis
Sarah R Barger1, Nils C Gauthier2, Mira Krendel1
1Cell and Developmental Biology Department, State University of New York Upstate Medical University, Syracuse, NY, USA.
Abstract:
Phagocytosis is a receptor-mediated, actin-dependent process of internalization of large extracellular particles, such as pathogens or apoptotic cells. Engulfment of phagocytic targets requires the activity of myosins, actin-dependent molecular motors, which perform a variety of functions at distinct steps during phagocytosis. By applying force to actin filaments, the plasma membrane, and intracellular proteins and organelles, myosins can generate contractility, directly regulate actin assembly to ensure proper phagocytic internalization, and translocate phagosomes or other cargo to appropriate cellular locations. Recent studies using engineered microenvironments and phagocytic targets have demonstrated how altering the actomyosin cytoskeleton affects phagocytic behavior. Here, we discuss how studies using genetic and biochemical manipulation of myosins, force measurement techniques, and live-cell imaging have advanced our understanding of how specific myosins function at individual steps of phagocytosis.
Insights
Myosins are essential molecular motors driving phagocytosis, the process of engulfing particles like pathogens. Research clarifies how these motors function in actin-dependent cellular internalization and cargo transport.
Area of Science:
- Cell Biology
- Molecular Biology
- Biophysics
Background:
- Phagocytosis is a critical cellular process for immune defense and tissue homeostasis.
- Myosins, as actin-dependent molecular motors, are integral to phagocytic events.
- The actomyosin cytoskeleton's role in phagocytosis is complex and multifaceted.
Purpose of the Study:
- To elucidate the specific roles of myosins in distinct stages of phagocytosis.
- To understand how myosin activity influences the internalization of large extracellular particles.
- To review recent advancements in studying myosin function during phagocytosis.
Main Methods:
- Genetic and biochemical manipulation of myosins.
- Force measurement techniques to quantify myosin-driven forces.
- Live-cell imaging to visualize dynamic cellular processes.
Main Results:
- Myosins generate contractility essential for engulfment.
- Myosins regulate actin assembly for efficient internalization.
- Myosins translocate phagosomes and other cellular cargo.
Conclusions:
- Specific myosins perform distinct functions at various steps of phagocytosis.
- Understanding myosin mechanics is key to deciphering phagocytic mechanisms.
- Engineered microenvironments and advanced imaging reveal myosin contributions to phagocytic behavior.
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