Abstract

Although macropinocytosis is widely recognized as a distinct form of fluid-phase endocytosis in antigen-presenting dendritic cells, it also occurs constitutively in many other normal and transformed cell types. Recent studies have established that various genetic or pharmacological manipulations can hyperstimulate macropinocytosis or disrupt normal macropinosome trafficking pathways, leading to accumulation of greatly enlarged cytoplasmic vacuoles. In some cases, this extreme vacuolization is associated with a unique form of non-apoptotic cell death termed “methuosis,” from the Greek methuo (to drink to intoxication). It remains unclear whether cell death related to dysfunctional macropinocytosis occurs in normal physiological contexts. However, the finding that some types of cancer cells are particularly vulnerable to this unusual form of cell death has raised the possibility that small molecules capable of altering macropinosome trafficking or function might be useful as therapeutic agents against cancers that are resistant to drugs that work by inducing apoptosis. Herein we review examples of cell death associated with dysfunctional macropinocytosis and summarize what is known about the underlying mechanisms.

Highlights

  • Macropinocytosis is a clathrin-independent endocytic process whereby mammalian cells internalize extracellular fluid inside vesicles formed by closure of actin-rich plasma membrane protrusions termed ruffles (Swanson and Watts, 1995; Kerr and Teasdale, 2009)

  • This process is best characterized in dendritic cells and macrophages, where it plays an important role in antigen uptake and processing

  • Hyperstimulation of macropinosome biogenesis, coupled with defects in the pathways for macropinosome recycling and/or maturation, results in extreme cytoplasmic vacuolization. This is followed by a unique form of cytolytic death that is somewhat selective for tumor cells and is distinct from apoptosis or other non-apoptotic cell death pathways

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Summary

Introduction

Macropinocytosis is a clathrin-independent endocytic process whereby mammalian cells internalize extracellular fluid inside vesicles formed by closure of actin-rich plasma membrane protrusions termed ruffles (Swanson and Watts, 1995; Kerr and Teasdale, 2009). These findings supported a model wherein constitutive Ras activation caused extreme endosomal vacuolization not just because of an increase in macropinocytotic activity, but because normal pathways for recycling and eventual lysosomal fusion of macropinosome-derived endosomal vesicles were impaired.

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