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Updated: Sep 4, 2025

In Situ Exploration of Murine Megakaryopoiesis using Transmission Electron Microscopy
Published on: September 8, 2021
Megapinosomes and homologous structures in hematopoietic cells
Andrea Bauer1, Giada Frascaroli2, Paul Walther3
1Central Facility for Electron Microscopy, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Abstract:
Megapinosomes are endocytic organelles found in human macrophage colony-stimulating factor (M-CSF) monocyte-derived M macrophages. They are large (several microns) and have a complex internal structure that is connected with the cytosol and consists of interconnected knots and concave bridges with sizes in the range of 100 nm. We called this structure trabecular meshwork. The luminal part of the megapinosome can be connected with luminal tubules and cisterns that form the megapinosome complex. The structures are especially well visible in scanning electron tomography when macrophages are prepared by high-pressure freezing and freeze substitution. Our research received a new impulse after studying the literature on hematopoietic cells, where very similar, most likely homologous, structures have been published in peritoneal macrophages as well as in megakaryocytes and blood platelets. In platelets, they serve as membrane storage that is used for structural changes of platelets during activation.
Insights
Megapinosomes, large endocytic organelles in macrophages, possess a complex internal trabecular meshwork. Similar structures in platelets suggest a conserved role in membrane dynamics across hematopoietic cells.
Area of Science:
- Cell Biology
- Macrophage Biology
- Endocytosis
Background:
- Megapinosomes are large endocytic organelles observed in M-CSF monocyte-derived macrophages.
- These organelles exhibit a complex internal structure termed the trabecular meshwork.
Purpose of the Study:
- To investigate the ultrastructure of megapinosomes.
- To explore potential homologous structures in other hematopoietic cells.
Main Methods:
- Scanning electron tomography was employed for high-resolution imaging.
- High-pressure freezing and freeze substitution were used for sample preparation.
Main Results:
- Megapinosomes feature a complex, interconnected trabecular meshwork (approx. 100 nm) linked to the cytosol.
- Luminal tubules and cisterns form a megapinosome complex.
- Homologous structures were identified in peritoneal macrophages, megakaryocytes, and platelets.
Conclusions:
- The trabecular meshwork represents a novel ultrastructural feature of megapinosomes.
- The presence of similar structures in platelets suggests a conserved function in membrane storage and cellular dynamics.
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