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Measuring the pH, Redox Chemistries, and Degradative Capacity of Macropinosomes using Dual-Fluorophore Ratiometric Microscopy
Published on: August 19, 2021
Macropinocytosis: Biology and mechanisms
1MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.
Abstract:
Macropinocytosis is a form of endocytosis performed by ruffles and cups of the plasma membrane. These close to entrap droplets of medium into micron-sized vesicles, which are trafficked through the endocytic system, their contents digested and useful products absorbed. Macropinocytosis is constitutive in certain immune cells and stimulated in many other cells by growth factors. It occurs across the animal kingdom and in amoebae, implying a deep evolutionary history. Its scientific history goes back 100 years, but increasingly work is focused on its medical importance in the immune system, cancer cell feeding, and as a backdoor into cells for viruses and drugs. Macropinocytosis is driven by the actin cytoskeleton whose dynamics can be appreciated with lattice light sheet microscopy: this reveals a surprising variety of routes for forming macropinosomes. In Dictyostelium amoebae, macropinocytic cups are organized around domains of PIP3 and active Ras and Rac in the plasma membrane. These attract activators of the Arp2/3 complex to their periphery, creating rings of actin polymerization that shape the cups. The size of PIP3 domains is controlled by RasGAPs, such as NF1, and the lipid phosphatase, PTEN. It is likely that domain dynamics determine the shape, evolution and closing of macropinocytic structures.
Insights
Macropinocytosis, a cellular uptake process, involves membrane structures engulfing extracellular fluid. Its regulation by lipid domains and actin dynamics is crucial for cell function and disease.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Macropinocytosis is a major endocytic pathway conserved across eukaryotes.
- It plays roles in nutrient uptake, immune responses, and pathogen entry.
- Its regulation involves complex signaling networks and cytoskeletal dynamics.
Purpose of the Study:
- To elucidate the molecular mechanisms governing macropinocytosis.
- To understand the role of lipid-protein interactions in macropinosome formation.
- To explore the evolutionary history and medical relevance of macropinocytosis.
Main Methods:
- Lattice light sheet microscopy to visualize actin dynamics.
- Biochemical assays to study lipid and protein interactions.
- Genetic manipulation in Dictyostelium discoideum.
Main Results:
- Actin cytoskeleton dynamics drive macropinosome formation.
- Plasma membrane domains rich in PIP3, Ras, and Rac organize macropinocytic cups.
- Arp2/3 complex activators at domain peripheries drive actin polymerization.
- RasGAPs (e.g., NF1) and PTEN regulate PIP3 domain size.
Conclusions:
- Macropinocytosis is a highly regulated process involving dynamic lipid and protein domains.
- Actin polymerization, orchestrated by these domains, shapes and closes macropinosomes.
- Understanding these mechanisms is key to targeting macropinocytosis in disease.
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