Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
2.
Nat Commun ; 12(1): 4838, 2021 08 10.
Article in English | MEDLINE | ID: mdl-34376698

ABSTRACT

Macropinosomes are formed by shaping actin-rich plasma membrane ruffles into large intracellular organelles in a phosphatidylinositol 3-kinase (PI3K)-coordinated manner. Here, we utilize lattice lightsheet microscopy and image visualization methods to map the three-dimensional structure and dynamics of macropinosome formation relative to PI3K activity. We show that multiple ruffling morphologies produce macropinosomes and that the majority form through collisions of adjacent PI3K-rich ruffles. By combining multiple volumetric representations of the plasma membrane structure and PI3K products, we show that PI3K activity begins early throughout the entire ruffle volume and continues to increase until peak activity concentrates at the base of the ruffle after the macropinosome closes. Additionally, areas of the plasma membrane rich in ruffling had increased PI3K activity and produced many macropinosomes of various sizes. Pharmacologic inhibition of PI3K activity had little effect on the rate and morphology of membrane ruffling, demonstrating that early production of 3'-phosphoinositides within ruffles plays a minor role in regulating their morphology. However, 3'-phosphoinositides are critical for the fusogenic activity that seals ruffles into macropinosomes. Taken together, these data indicate that local PI3K activity is amplified in ruffles and serves as a priming mechanism for closure and sealing of ruffles into macropinosomes.


Subject(s)
Cell Membrane/metabolism , Microscopy, Fluorescence/methods , Phosphatidylinositol 3-Kinases/metabolism , Pinocytosis/physiology , Animals , Cell Membrane/drug effects , Cells, Cultured , Chromones/pharmacology , Enzyme Inhibitors/pharmacology , HEK293 Cells , Humans , Macrophages/cytology , Macrophages/metabolism , Macrophages/ultrastructure , Mice , Microscopy, Electron, Scanning , Morpholines/pharmacology , Phosphatidylinositols/metabolism , Pinocytosis/drug effects , RAW 264.7 Cells
SELECTION OF CITATIONS
SEARCH DETAIL
...