Cytonemes |
In cell culture |
|
|
|
|
|
|
|
Xenopus fibroblasts |
Wnt2b–EGFP |
Wnt secretion |
n/a |
Actin and microtubules |
Holzer et al. (2012) |
|
Mouse C3H/10T1/2 mesenchymal cells |
FGF: FGFR elongation via cytonemes |
FGF reception |
Up to > 60 µm; n/a |
Actin |
Koizumi et al. (2012) |
|
Zebrafish pigment cells |
Membrane-associated signal to trigger depolarization |
Pigment pattern formation |
20–30 µm; n/a |
Actin |
Hamada et at. (2014) |
In tissue |
|
|
|
|
|
|
|
Wing disc tracheal cells or peripodial layer of the eye disc |
Dpp/Tkv; Spi/EgfR reception |
Imaginal disc pattering |
Up to > 80 µm; 200 nm |
Actin |
Sato and Kornberg et al. (2002); Hsiung et al. (2005); Roy et al. (2011) |
|
Drosophila myoblasts |
Wg/Fzd uptake and delta/notch interaction |
Relay system for Wg and Notch signals |
Up to 25 µm; 200 nm |
Actin |
Huang and Kornberg (2015) |
|
Drosophila germ cells |
Dpp transport |
Maintenance of stem cells |
Up to 4 µm |
Microtubules |
Inaba et al. (2015) |
|
Basal cytonemes in the Drosophila wing pouch |
Hh/patched reception |
Imaginal disc pattering |
Up to 70 µm; n/a |
Actin |
Bischoff et al. (2013); Gradilla et al. (2014); González-Méndez et al. (2017) |
|
Zebrafish neural plate |
Wnt transport to Fzd/Lrp6 containing cells |
Neuroectoderm AP patterning |
Up to 50 µm; <1.5 µm |
Actin |
Stanganello et al. (2015), Mattes et al. (2018) |
|
Chick limb bud |
Shh ligand caintaining cytonemes connect Cdo and Boc coreceptors cytonemes |
Patterning of mesenchymal cells |
Up to 150 µm; 200 nm |
Actin |
Sanders et al. (2013) |
Tunnelling nanotubes |
In cell culture |
|
|
|
|
|
|
|
Primary rat pheochromocytoma (PC12) |
Membrane vesicles, membrane-anchored proteins, and small organelles |
Intercellular transfer of cellular components |
Thin: 20 µm; 70–200 nm |
Actin |
Rustom et al. (2004) |
|
Primary rat pheochromocytoma (PC12) |
Mitochondria and intracellular vesicles such as endosomes and lysosomes |
Recovery mechanism for stressed cells |
Thick: n/a; > 700 nm |
Actin and microtubules |
Wang and Gerdes (2015) |
|
Human monocyte-derived macrophages |
Mitochondria and intracellular vesicles |
Intercellular transfer of cellular components |
Thick: n/a; > 700 nm |
Actin and microtubules |
Onfelt et al. (2006) |
|
Humanperipheral blood NK cells, macrophages, and B cells |
Bacteria ; GFP-tagged cell surface class I MHC protein |
Communication mechanism in immunology |
10–50 µm; <700 nm |
Actin |
Onfelt et al. (2006) |
|
Between adult human endothelial progenitor cells and neonatal rat cardiomyocytes |
Mitochondria, soluble GFP |
Cell fate decisions in adult progenitor cells |
Up to 120 µm; 50–800 nm |
Actin |
Koyanagi et al. (2005) |
|
Neuronal CAD cells and between astrocytes to granule neurons |
PrPSC prions |
Propagation of infectious particles |
Up to 80 µm; 180–800 nm |
Actin |
Gousset et al. (2009); Zhu et al. (2015) |
|
NRK cells, HEK293, HUVEC, and NCC |
Electrical signals |
Electrical coupling via gap junctions |
Up to 70 µm; 50–200 nm |
Actin |
Wang et al. (2010) |
In tissue |
|
|
|
|
|
|
|
Neural Crest cells in chick embryos |
Cytoplasmic material; cytosolic and membrane-tethered fluorescent proteins |
Delivering positional information during migration |
Up to 100 µm; 0.5–2 µm |
N/a |
Teddy and Kulesa (2004); McKinney et al. (2011) |
|
Gastrulating zebrafish embryo cells |
Cytosolic and membrane-tethered fluorescent proteins |
Cell–cell communication during gastrulation |
Up to 350 µm; <1 µm |
Actin; tubulin only in proximal part |
Caneparo et al. (2011) |
|
Myeloid cells in the mouse cornea |
Smaller molecules such as MHC and/or MHC-antigen complexes |
Immunological response |
> 300 µm; 200–300 nm |
Actin; n/a |
Chinnery et al. (2008); Seyed-Razavi et al. (2013) |
|
Patient-derived malignant pleural mesothelioma |
Organelles and other cytosolic components |
Role in pathogenesis and invasion |
Up to 100–200 µm; n/a |
Actin; n/a |
Lou et al. (2012) |