Atunneling nanotube(TNT) ormembrane nanotube is a term that has been applied to cytoskeletal protrusions that extend from theplasma membrane which enable different animal cells to connect over long distances, sometimes over 100μm between certain types of cells.^[2][3][4] Tunneling nanotubes that are less than 0.7 micrometers in diameter, have anactin structure and carry portions ofplasma membrane between cells in both directions. Larger TNTs (>0.7 μm) contain an actin structure withmicrotubules and/orintermediate filaments, and can carry components such asvesicles andorganelles between cells, includingwhole mitochondria.^[5][6][7] The diameter of TNTs ranges from 0.05 μm to 1.5 μm and they can reach lengths of several cell diameters.^[7][8] There have been two types of observed TNTs: open ended and closed ended. Open ended TNTs connect the cytoplasm of two cells. Closed ended TNTs do not have continuous cytoplasm as there is a gap junction cap that only allows small molecules and ions to flow between cells.^[9] These structures have shown involvement in cell-to-cell communication, transfer ofnucleic acids such asmRNA andmiRNA between cells in culture or in atissue, and the spread of pathogens or toxins such asHIV andprions.^{[10][11][12][13][14][3]} TNTs have observed lifetimes ranging from a few minutes up to several hours, and several proteins have been implicated in their formation and inhibition, including many that interact with Arp2/3.^[15][16]

Membrane nanotubes were first described in a 1999Cell article examining the development ofDrosophila melanogaster wingimaginal discs.^[17] More recently, aScience article published in 2004 described structures that connectedPC12 cells together, as well as other types of cell cultures.^[7][18] This study coined the term "tunneling nanotubes" and also showed that nanotube formation between cells is correlated with both membrane and organelle transfer.^[7] Since these publications, more TNT-like structures have been recorded, containing varying levels of F-actin, microtubules and other components, but remaining relatively homogenous in terms of composition.^[15]

Several mechanisms may be involved in nanotube formation. These include molecular controls as well as cell-to-cell interactions.

Two primary mechanisms for TNT formation have been proposed. The first involves cytoplasmic protrusions extending from one cell to another, where they fuse with the membrane of the target cell.^[7] The other mechanism occurs when two previously connected cells move away from one another, and TNTs remain as bridges between the two cells.^[3][19]

Somedendritic cells and THP-1monocytes have been shown to connect via tunneling nanotubes and display evidence of calcium flux when exposed to bacterial or mechanical stimuli. TNT-mediated signaling has shown to produce spreading in target cells, similar to thelamellipodia produced when dendritic cells are exposed to bacterial products. The TNTs demonstrated in this study propagated at initial speed of 35 micrometers/second and have shown to connect THP-1 monocytes with nanotubes up to 100 micrometers long.^[20]

Phosphatidylserine exposure has demonstrated the ability to guide TNT formation frommesenchymal stem cells (MSCs) to a population of injured cells.^[21] The proteinS100A4 and its receptor have been shown to guide the direction of TNT growth, asp53 activatescaspase 3 to cleave S100A4 in the initiating cell, thereby generating a gradient in which the target cell has higher amounts of the protein.^[22] These findings suggests that chemotactic gradients may be involved in TNT induction.

One study found that cell-to-cell contact was necessary for the formation of nanotube bridges betweenT cells.^[3] p53 activation has also been implicated as a necessary mechanism for the development of TNTs, as the downstream genes up-regulated by p53 (namelyEGFR,Akt,PI3K, andmTOR) were found to be involved in nanotube formation followinghydrogen peroxide treatment and serum starvation.^[23]Connexin-43 has shown to promote connection betweenbone marrow stromal cells (BMSCs) andalveolar epithelial cells, leading to the formation of nanotubes.^[24]

Cellular stress byrotenone orTNF-α was also shown to induce TNT formation between epithelial cells.^[25] Inflammation bylipopolysaccharides orinterferon-γ has shown to increase the expression of proteins related to TNT formation.^[26]

While TNTs have many components, their main inhibitors work by blocking or limiting actin formation. TNT-like structures called streamers, which are extremely thin protrusions, did not form when cultured withcytochalasin D, an F-actindepolymerizing compound.^[27][28] A separate study usingcytochalasin B found that it impacted TNT formation without the destruction of existing TNTs.^[29]Latrunculin-B, another F-actin depolymerizing compound, was found to completely block TNT formation.^[7] BlockingCD38, which had been implicated in the release of mitochondria byastrocytes, also significantly decreased TNT formation.^[30][31]

TNFAIP2, also called M-Sec, is known to mediate TNT formation, and knockdown of this protein byshRNA reduced TNT development inepithelial cells by about two-thirds.^[26]

Inhibiting Arp2/3 directly resulted in different effects depending on cell type. In human eye cells and macrophages, blocking Arp2/3 led to a decrease in TNT formation. However, such inhibition in neuronal cells resulted in an increase in the amount of cells connected via TNTs, while lowering the total amount of TNTs connecting cells.^[32]

Tunneling nanotubes have been implicated as one mechanism by which wholemitochondria can betransferred from cell to cell.^[7] A recent study inNature Nanotechnology has reported that cancer cells can hijack the mitochondria from immune cells via physical tunneling nanotubes.^[34]Mitochondrial DNA damage appears to be the main trigger for the formation of TNTs in order to traffic entire mitochondria, though the exact threshold of damage necessary to induce TNT formation is yet unknown.^[35] The maximum speed of mitochondria traveling over TNTs was found to be about 80nm/s, lower than the measured speed of 100-1400 nm/s ofaxonal transport of mitochondria; this could be due to the smaller diameter of TNTs inhibiting mitochondrial migration.^[36]

In one study, Ahmadet al. used four lines of mesenchymal stem cells, each expressing either a differing phenotype of theRho-GTPase Miro1; a higher level of Miro1 was associated with more efficientmitochondrial transfer via TNTs.^[25] Several studies have shown, through the selective blockage of TNT formation, that TNTs are a primary mechanism for the trafficking of whole mitochondria between heterogeneous cells.^[37][38][39]

One use of this phenomenon is in the recovery fromheart attacks.^[40] When cardiac muscle cells are injured by oxygen deprivation, the damaged mitochondria release reactive oxygen species, which trigger nearby mesenchymal stem cells to produce and donate healthy mitochondria to the damaged muscle cells through TNTs.^[40]

Tunneling nanotubes have been shown to propagate action potentials via their extensions of endoplasmic reticulum that propagate Ca²⁺ influx through active diffusion.^[41]

Many viruses can transfer their proteins to TNT-connected cells. Certain types, such as influenza, have even been found to transfer their genome via TNTs.^[42] Over two dozen types of viruses have been found to transfer through and/or modulate TNT.^[43] A 2022 study suggests thatSARS-CoV-2 builds tunneling nanotubes from nose cells to gain accessto the brain.^[44][45]

HIV also appears to spread through TNTs, specifically betweendendritic cells.^[40] Researchers have found that "Long-term nonprogressors" of HIV, who can control the virus without antiretroviral therapy, have a defect in their dendritic cells' ability to create TNTs.^[40]

Prions can also spread through TNTs.^[40]

Tunneling nanotubes have the potential to be involved in applications of nanomedicine, as they have shown the ability to transfer such treatments between cells. Future applications look to either inhibit TNTs to prevent nanomedicine toxicity from reaching neighboring cells, or to promote TNT formation to increase positive effects of the medicine.^[46]

While TNT-like structures are all made of cytoskeletal cellular protrusions, their fundamental difference with TNTs is in the connection between two cells. TNT-like structures do not share intracellular contents such as ions or small molecules between connected cells–a feature that is present in both open ended and closed ended TNTs.^[9]

A TNT-like structure called acytoneme enables exchanges between signaling centers. The formation of cytonemes towards aFGF homolog gradient has been observed, suggesting thatchemotactic controls may also induce the formation of TNT-like structures.^[17] Cytonemes, however, do not always connect the membrane two cells and can act solely as environmental sensors.^[28]

Plasmodesmata have been identified as functional channels interconnecting plant cells, andstromules interconnectplastids.^[47][48]

Myopodia are actin-rich cytoplasmic extensions which have been observed in embryonicDrosophila. Similar structures have been observed inXenopus andmouse models.^[15] Actin-containing cellular protrusions dubbed "streamers" have been observed in culturedB cells.^[28]

Vesicular transport in membrane nanotubes has been modeled utilizing a continuum approach.^[49] A variety of synthetic nanotubes, based on stacking of cyclic peptides and other cyclic molecules, have been investigated.^[50]

• Horizontal transfer of mitochondria

• Hans-Hermann Gerdes Research Group - The laboratory that first observed membrane nanotubes

• Cell anatomy
• Membrane biology

• Articles with short description
• Short description is different from Wikidata