Related Experiment Video
Updated: Mar 27, 2026

11:01
Automated Imaging and Analysis for the Quantification of Fluorescently Labeled Macropinosomes
Published on: August 24, 2021
3.5K
Megapinocytosis: a novel endocytic pathway
Andrea Bauer1, Narmadha Subramanian1,2, Clarissa Villinger1,2
1Institute of Virology, University Medical Center Ulm, Albert-Einstein-Allee, 89081, Ulm, Germany.
Histochemistry and Cell Biology
|January 7, 2016
Summary
M2 macrophages form unique large endocytotic structures called megapinosomes, distinct from typical macropinosomes. These structures, observed during human cytomegalovirus infection, were absent in M1 macrophages.
Area of Science:
- Cell Biology
- Immunology
- Macrophage Biology
Background:
- Macrophages are key immune cells with diverse functions.
- M2 macrophages are involved in tissue repair and immune modulation.
- Endocytosis is a crucial cellular process for nutrient uptake and signaling.
Purpose of the Study:
- To characterize novel large endocytotic structures in M2 macrophages.
- To investigate the formation and ultrastructure of these structures.
- To determine if these structures are associated with specific stimuli like human cytomegalovirus.
Main Methods:
- Scanning electron microscopy (SEM) for surface morphology.
- Transmission electron microscopy (TEM) with high-pressure freezing for ultrastructure.
- Comparative analysis between M1 and M2 macrophages.
Main Results:
- M2 macrophages form large endocytotic structures named megapinosomes (several micrometers in diameter).
- Megapinosome formation involves plasma membrane invagination and closure by microvilli-like structures.
- Ultrastructural analysis revealed a trabecular meshwork within megapinosomes, topologically linked to the cytosol.
- Megapinosome formation increased upon human cytomegalovirus inoculation in M2 macrophages.
- Megapinosomes were not observed in M1 macrophages.
Conclusions:
- Megapinosomes represent a distinct form of endocytosis in M2 macrophages.
- Megapinosome formation is specific to M2 macrophages and can be induced by human cytomegalovirus.
- These findings offer new insights into M2 macrophage endocytic mechanisms and their role in immune responses.
Related Concept Videos
Pinocytosis
5.1K
Cells use energy-requiring bulk transport mechanisms to transfer large particles or large numbers of small particles into or out of the cell. The cells envelop the particles in spherical membranes called vesicles or vacuoles. Vesicles that transport material into the cell are built from the cell membrane. These vesicles encapsulate external molecules and transport them into the cell in a process called endocytosis.
Pinocytosis ("cellular drinking") is one of three main types of...
Pinocytosis ("cellular drinking") is one of three main types of...
5.1K
Pinocytosis
72.0K
Cells use energy-requiring bulk transport mechanisms to transfer large particles, or large amounts of small particles, into or out of the cell. The cells envelop the particles in spherical membranes called vesicles or vacuoles. Vesicles that transport material into the cell are built from the cell membrane. These vesicles encapsulate external molecules and transport them into the cell in a process called endocytosis.
72.0K
Receptor-mediated Endocytosis
113.4K
Overview
113.4K
Receptor-mediated Endocytosis
11.6K
Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
11.6K
Receptor-Mediated Endocytosis
5.7K
5.7K
Pinching-off of Coated Vesicles
4.4K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
4.4K

