Abstract

Using the optogenetic photo-manipulation of photoactivatable (PA)-Rac1, remarkable cell surface ruffling and the formation of a macropinocytic cup (premacropinosome) could be induced in the region of RAW264 macrophages irradiated with blue light due to the activation of PA-Rac1. However, the completion of macropinosome formation did not occur until Rac1 was deactivated by the removal of the light stimulus. Following PA-Rac1 deactivation, some premacropinosomes closed into intracellular macropinosomes, whereas many others transformed into long Rab10-positive tubules without forming typical macropinosomes. These Rab10-positive tubules moved centripetally towards the perinuclear Golgi region along microtubules. Surprisingly, these Rab10-positive tubules did not contain any endosome/lysosome compartment markers, such as Rab5, Rab7, or LAMP1, suggesting that the Rab10-positive tubules were not part of the degradation pathway for lysosomes. These Rab10-positive tubules were distinct from recycling endosomal compartments, which are labeled with Rab4, Rab11, or SNX1. These findings suggested that these Rab10-positive tubules may be a part of non-degradative endocytic pathway that has never been known. The formation of Rab10-positive tubules from premacropinosomes was also observed in control and phorbol myristate acetate (PMA)-stimulated macrophages, although their frequencies were low. Interestingly, the formation of Rab10-positive premacropinosomes and tubules was not inhibited by phosphoinositide 3-kinase (PI3K) inhibitors, while the classical macropinosome formation requires PI3K activity. Thus, this study provides evidence to support the existence of Rab10-positive tubules as a novel endocytic pathway that diverges from canonical macropinocytosis.

Highlights

  • Macropinocytosis is a form of clathrin-independent, actindependent endocytosis that mediates the non-selective uptake of extracellular fluids and solutes into 0.2 – several mm diameter endocytic vesicles called macropinosomes

  • When we observed enhanced green fluorescent protein (EGFP)-Rab10 dynamics in RAW264 cells co-expressing with mCherry-photoactivatable Rac1 (PA-Rac1), which was temporally activated by 488 nm excitation for EGFP-Rab10 observation with 15-sec intervals, we found that the Rab10-positive tubules frequently form from the Rab10-positive premacropinosomes (Figures 1C, D)

  • We first identified a novel endocytic pathway that diverges from canonical macropinocytosis using the optogenetic photo-manipulation of Rac1 activity

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Summary

Introduction

Macropinocytosis is a form of clathrin-independent, actindependent endocytosis that mediates the non-selective uptake of extracellular fluids and solutes into 0.2 – several mm diameter endocytic vesicles called macropinosomes. In macrophages and dendritic cells, this endocytic pathway is involved in immune surveillance and antigen presentation [3]. Macropinocytosis has been proposed to be involved in the uptake and propagation of pathogenic protein aggregates associated with neurodegenerative diseases such as Alzheimer’s disease and Parkinson’s disease [5]. Many pathogenic bacteria and viruses exploit macropinocytosis pathways to gain entry into host cells during infection [6]. A better understanding of the molecular mechanisms underlying macropinocytosis and its related pathways has implications for cell biology and the establishment of therapeutic strategies to combat various diseases, including cancer and viral infections

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