On phagosome individuality and membrane signalling networks
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Updated: Aug 23, 2026

"Phagosome Closure Assay" to Visualize Phagosome Formation in Three Dimensions Using Total Internal Reflection Fluorescent Microscopy (TIRFM)
Published on: August 26, 2016
1EMBL, Meyerhofstrasse 1, Postfach 102209, 69117 Heidelberg, Germany. griffiths@embl.de
Abstract:
Cells such as macrophages take up pathogens into specialized membrane organelles (phagosomes) that fuse with other organelles, including lysosomes, in a process termed maturation. The fully matured phagolysosome is a low-pH, hydrolase-rich killing device that some pathogens can bypass. One might expect that phagosomes containing a given type of particle that entered cells simultaneously via the same receptor would behave the same, at least in a single cell. Surprisingly, however, recent data show that phagosomes formed via the same receptors can find themselves in different chemical states even within the same macrophage. Here, I argue that each phagosome is an individual entity whose behaviour depends on a finite number of stable equilibrium states in its membrane signalling networks.
Insights
Phagosomes, cellular compartments engulfing pathogens, exhibit surprising chemical diversity within macrophages. This study proposes each phagosome
Area of Science:
- Cell biology
- Immunology
- Pathogen-host interactions
Background:
- Macrophages engulf pathogens into phagosomes, which mature into antimicrobial phagolysosomes.
- Pathogens can evade the host immune response by interfering with phagosome maturation.
- Phagosomes are expected to follow similar maturation pathways, especially when formed simultaneously via the same receptor.
Purpose of the Study:
- To investigate the surprising heterogeneity observed in phagosome chemical states within a single macrophage.
- To propose a model explaining the divergent maturation pathways of similarly formed phagosomes.
Main Methods:
- Analysis of existing data on phagosome maturation dynamics.
- Theoretical modeling of membrane signaling networks within individual phagosomes.
Main Results:
- Phagosomes generated through identical receptors display distinct chemical properties and maturation trajectories.
- This heterogeneity persists even within the same macrophage cell.
- A model is proposed where individual phagosomes exist in discrete, stable signaling states.
Conclusions:
- Each phagosome represents an individual entity with unique behavior, not a uniform population.
- Phagosome behavior is dictated by intrinsic signaling networks, leading to stable equilibrium states.
- Understanding this individuality is crucial for comprehending host-pathogen interactions and immune evasion strategies.
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