Skip to main content
. 2012 Aug 30;28(9):1723–1737. doi: 10.1007/s00467-012-2281-y

Table 1.

Mechanisms of endocytosis

Pathway Morphology and size Coat Small GTPase Cargo Function
Clathrin-mediateda Vesicular 150–200 nm Clathrin Rab5 RTKs, GPCR, TGF-ßR, Notch, TfR, LDLR, ß-arrestin, Wnt/ß-catenin Cell signaling, vesicular transport
Caveolae-mediateda Flask-shaped 50–120 nm Caveolin 1 and 2 Unclear GPI-APs, TGF-ßR, CTxB, viruses, folic acid, IGF-1R, Wnt/ß-catenin Cell signaling, lipid regulation, vesicular transport, transcytosis
CLIC/GEEC Tubular None Cdc42 Arf1 GPI-APs, glycosphingolipids, cholera toxin Actin dynamics and cellular stress pathways, differentiation and apoptosis, focal adhesion, fluid-phase uptake, oncogenesis
Arf6-mediated Tubular None Arf6 ß-arrestins, MHC I-II Membrane curvature
Flotillin-mediated Vesicular Flotillin 1 and 2 None CTxB, GPI-AP, proteoglycans Lipid raft-mediated endocytosis,
IL-2Ra Vesicular 50–100 nm None RhoA, Rac1 IL-2Rß, yc cytokine receptor IL-2R endocytosis and signaling
Macropinocytosisa Ruffled None Rac1, Cdc42, Arf6, Rab5 Fluid, RTKs, bacteria Extracellular fluid uptake, actin dynamics
Phagocytosis Cargo shaped None Rac1, RhoA, Cdc42 Nutrients, pathogens, dead cells, and cellular debris Uptake of nutrients, pathogens, and cellular debris by professional phagocytic cells; opsonization of foreign particles followed by actin rearrangements

Arf, ADP rybosylation factor; GTPase, guanine triphosphate hydrolyze; Cdc42, cell division control protein 42 homolog; CLIC, clathrin-independent carriers; CTxB, cholera toxin B subunit; GEEC, GPI-AP-enriched early endosomal compartment; GPI-APs, glycosphingolipids anchored proteins; GPCR, G-protein coupled receptor; Rab, ras-associated binding protein; IGF-1R, insulin growth factor-1 receptor; IL-2R, interleukin 2 receptor beta; TRKs, receptor tyrosine kinases; TfR, transferring receptor; LDLR, low-density lipoprotein receptor; MHC, Major histocompatibility complex; RhoA, Ras homolog gene family, member A; Rac1, Ras-related C3 botulinum toxin substrate 1; TGF-ßR, transforming growth factor beta receptor

amarks the dynamin-dependent mechanisms; macropinocytosis requires dynamin only in some situations. The above information is based on references listed in this manuscript (most extensively reviewed in refs. [1, 2]. Only selected cargo and functions are listed