| Literature DB >> 26733077 |
Andrea Bauer1, Narmadha Subramanian1,2, Clarissa Villinger1,2, Giada Frascaroli1, Thomas Mertens1, Paul Walther3.
Abstract
M2 macrophages showed large endocytotic structures, very different from classical macropinosomes that we named megapinosomes. As observed in the scanning electron microscope, megapinosome formation started with a large (diameter of several micrometers) invagination of the plasma membrane. When the invagination was almost completed, the remaining opening was closed by an actinomorphous centripetal arrangement of many (about 50-100) microvilli-like structures. In transmission electron microscopy using high-pressure freezing, we observed that the megapinosome was filled with a trabecular meshwork that originated from the highly structured plasma membrane. The trabecular meshwork was topologically part of the cytosol and separated from the extracellular fluid by a lipid bilayer. According to ultrastructural features, we could define different phases of megapinosome formation and decay. Megapinosomes became more frequent when M2 macrophages were inoculated with human cytomegalovirus. We did not find megapinosome formation in M1 macrophages.Entities:
Keywords: Electron microscopy; Endocytosis; High-pressure freezing; Macrophages; Macropinocytosis; SEM; TEM
Mesh:
Year: 2016 PMID: 26733077 DOI: 10.1007/s00418-015-1395-2
Source DB: PubMed Journal: Histochem Cell Biol ISSN: 0948-6143 Impact factor: 4.304