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Updated: May 9, 2026

Automated Imaging and Analysis for the Quantification of Fluorescently Labeled Macropinosomes
Published on: August 24, 2021
Dissecting the roles of Rac1 activation and deactivation in macropinocytosis using microscopic photo-manipulation
Makoto Fujii1, Katsuhisa Kawai, Youhei Egami
1Department of Histology and Cell Biology, School of Medicine, Kagawa University, Miki, Kagawa 761-0793, Japan.
Abstract:
Macropinocytosis, a fluid-phase endocytosis, is a crucial pathway for antigen uptake and presentation in macrophages. We attempted to characterise the activation and deactivation of a small GTPase molecular switch, Rac1, in macropinocytosis using microscopic photo-manipulation. Expression of genetically encoded photoactivatable-Rac1 (PA-Rac1) in RAW264 macrophages enabled the local, reversible control of macropinocytosis using blue laser irradiation. Marked membrane ruffling and unclosed pre-macropinosomes were observed in the irradiated region of macrophages under the persistent activation of PA-Rac1. Although phosphatidylinositol 4,5-bisphosphate and actin were also localised to this region, the recruitment of maturating endosome markers, such as phosphatidylinositol 3-phosphate and Rab21, was restricted until PA-Rac1 deactivation. After deactivating PA-Rac1 by ceasing irradiation, membrane ruffling immediately receded, and the macropinosomes acquired maturation markers. These data suggest that activation of Rac1 is sufficient to induce membrane ruffling and macropinocytic cup formation, but subsequent deactivation of Rac1 is required for macropinosome closure and further maturation.
Insights
Rac1 activation drives membrane ruffling and macropinocytic cup formation in macrophages. However, Rac1 deactivation is essential for macropinosome closure and maturation, revealing its role in endocytosis.
Area of Science:
- Cell Biology
- Immunology
- Molecular Biology
Background:
- Macropinocytosis is a key process for antigen uptake and presentation by macrophages.
- Small GTPases, like Rac1, act as molecular switches regulating cellular processes.
Purpose of the Study:
- To investigate the role of Rac1 activation and deactivation in macropinocytosis.
- To characterize the spatiotemporal control of macropinocytosis using photo-manipulation.
Main Methods:
- Utilized photoactivatable-Rac1 (PA-Rac1) expressed in RAW264 macrophages.
- Employed blue laser irradiation for local and reversible control of PA-Rac1.
- Microscopic analysis to observe membrane dynamics and endosome maturation markers.
Main Results:
- Persistent Rac1 activation induced membrane ruffling and unclosed pre-macropinosomes.
- Maturation markers were restricted until Rac1 deactivation.
- Rac1 deactivation led to immediate cessation of ruffling and macropinosome maturation.
Conclusions:
- Rac1 activation is sufficient for initiating membrane ruffling and macropinocytic cup formation.
- Subsequent Rac1 deactivation is necessary for macropinosome closure and maturation.
- This study elucidates the dynamic regulation of macropinocytosis by Rac1.
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