Oxidative stress and Rho GTPases in the biogenesis of tunnelling nanotubes: implications in disease and therapy

. 2021 Dec 18 ; 79 (1) : 36. [epub] 20211218

Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid34921322

Grantová podpora
TMA-Pi PhD Scholarship Manipal University
MAHE/CDS/PHD/MIFR/2019 Manipal University
5/4-5/Ad-hoc/Neuro/216/2020-NCD-I Indian Council of Medical Research

Odkazy

PubMed 34921322
PubMed Central PMC8683290
DOI 10.1007/s00018-021-04040-0
PII: 10.1007/s00018-021-04040-0
Knihovny.cz E-zdroje

Tunnelling nanotubes (TNTs) are an emerging route of long-range intercellular communication that mediate cell-to-cell exchange of cargo and organelles and contribute to maintaining cellular homeostasis by balancing diverse cellular stresses. Besides their role in intercellular communication, TNTs are implicated in several ways in health and disease. Transfer of pathogenic molecules or structures via TNTs can promote the progression of neurodegenerative diseases, cancer malignancy, and the spread of viral infection. Additionally, TNTs contribute to acquiring resistance to cancer therapy, probably via their ability to rescue cells by ameliorating various pathological stresses, such as oxidative stress, reactive oxygen species (ROS), mitochondrial dysfunction, and apoptotic stress. Moreover, mesenchymal stem cells play a crucial role in the rejuvenation of targeted cells with mitochondrial heteroplasmy and oxidative stress by transferring healthy mitochondria through TNTs. Recent research has focussed on uncovering the key regulatory molecules involved in the biogenesis of TNTs. However further work will be required to provide detailed understanding of TNT regulation. In this review, we discuss possible associations with Rho GTPases linked to oxidative stress and apoptotic signals in biogenesis pathways of TNTs and summarize how intercellular trafficking of cargo and organelles, including mitochondria, via TNTs plays a crucial role in disease progression and also in rejuvenation/therapy.

Zobrazit více v PubMed

Rustom A, Saffrich R, Markovic I, Walther P, Gerdes HH. Nanotubular highways for intercellular organelle transport. Science. 2004;303(5660):1007–1010. doi: 10.1126/science.1093133. PubMed DOI

Gerdes HH, Rustom A, Wang X. Tunneling nanotubes, an emerging intercellular communication route in development. Mech Dev. 2013;130(6–8):381–387. doi: 10.1016/j.mod.2012.11.006. PubMed DOI

Ljubojevic N, Henderson JM, Zurzolo C. The ways of actin: why tunneling nanotubes are unique cell protrusions. Trends Cell Biol. 2021;31(2):130–142. doi: 10.1016/j.tcb.2020.11.008. PubMed DOI

Roehlecke C, Schmidt MHH. Tunneling nanotubes and tumor microtubes in cancer. Cancers (Basel) 2020;12(4):857. doi: 10.3390/cancers12040857. PubMed DOI PMC

Sartori-Rupp A, Cordero Cervantes D, Pepe A, Gousset K, Delage E, Corroyer-Dulmont S, et al. Correlative cryo-electron microscopy reveals the structure of TNTs in neuronal cells. Nat Commun. 2019;10(1):342. doi: 10.1038/s41467-018-08178-7. PubMed DOI PMC

Mittal R, Karhu E, Wang JS, Delgado S, Zukerman R, Mittal J, et al. Cell communication by tunneling nanotubes: implications in disease and therapeutic applications. J Cell Physiol. 2019;234(2):1130–1146. doi: 10.1002/jcp.27072. PubMed DOI

Victoria GS, Zurzolo C. The spread of prion-like proteins by lysosomes and tunneling nanotubes: implications for neurodegenerative diseases. J Cell Biol. 2017;216(9):2633–2644. doi: 10.1083/jcb.201701047. PubMed DOI PMC

Valdinocci D, Kovarova J, Neuzil J, Pountney DL. Alpha-synuclein aggregates associated with mitochondria in tunnelling nanotubes. Neurotox Res. 2021;39(2):429–443. doi: 10.1007/s12640-020-00285-y. PubMed DOI

Ahmad T, Mukherjee S, Pattnaik B, Kumar M, Singh S, Kumar M, et al. Miro1 regulates intercellular mitochondrial transport and enhances mesenchymal stem cell rescue efficacy. EMBO J. 2014;33(9):994–1010. PubMed PMC

Spees JL, Olson SD, Whitney MJ, Prockop DJ. Mitochondrial transfer between cells can rescue aerobic respiration. Proc Natl Acad Sci USA. 2006;103(5):1283–1288. doi: 10.1073/pnas.0510511103. PubMed DOI PMC

Zhu D, Tan KS, Zhang X, Sun AY, Sun GY, Lee JC. Hydrogen peroxide alters membrane and cytoskeleton properties and increases intercellular connections in astrocytes. J Cell Sci. 2005;118(Pt 16):3695–3703. doi: 10.1242/jcs.02507. PubMed DOI

Wang Y, Cui J, Sun X, Zhang Y. Tunneling-nanotube development in astrocytes depends on p53 activation. Cell Death Differ. 2011;18(4):732–742. doi: 10.1038/cdd.2010.147. PubMed DOI PMC

Zhang S, Kazanietz MG, Cooke M. Rho GTPases and the emerging role of tunneling nanotubes in physiology and disease. Am J Physiol Cell Physiol. 2020;319(5):C877–C884. doi: 10.1152/ajpcell.00351.2020. PubMed DOI PMC

Olson MF, Ashworth A, Hall A. An essential role for Rho, Rac, and Cdc42 GTPases in cell cycle progression through G1. Science. 1995;269(5228):1270–1272. doi: 10.1126/science.7652575. PubMed DOI

Fransson A, Ruusala A, Aspenstrom P. Atypical Rho GTPases have roles in mitochondrial homeostasis and apoptosis. J Biol Chem. 2003;278(8):6495–6502. doi: 10.1074/jbc.M208609200. PubMed DOI

Nahacka Z, Zobalova R, Dubisova M, Rohlena J, Neuzil J. Miro proteins connect mitochondrial function and intercellular transport. Crit Rev Biochem Mol Biol. 2021;56(4):401–425. doi: 10.1080/10409238.2021.1925216. PubMed DOI

Biran A, Perelmutter M, Gal H, Burton DG, Ovadya Y, Vadai E, et al. Senescent cells communicate via intercellular protein transfer. Genes Dev. 2015;29(8):791–802. doi: 10.1101/gad.259341.115. PubMed DOI PMC

Watkins SC, Salter RD. Functional connectivity between immune cells mediated by tunneling nanotubules. Immunity. 2005;23(3):309–318. doi: 10.1016/j.immuni.2005.08.009. PubMed DOI

Thayanithy V, Dickson EL, Steer C, Subramanian S, Lou E. Tumor-stromal cross talk: direct cell-to-cell transfer of oncogenic microRNAs via tunneling nanotubes. Transl Res. 2014;164(5):359–365. doi: 10.1016/j.trsl.2014.05.011. PubMed DOI PMC

Koyanagi M, Brandes RP, Haendeler J, Zeiher AM, Dimmeler S. Cell-to-cell connection of endothelial progenitor cells with cardiac myocytes by nanotubes: a novel mechanism for cell fate changes? Circ Res. 2005;96(10):1039–1041. doi: 10.1161/01.RES.0000168650.23479.0c. PubMed DOI

Onfelt B, Nedvetzki S, Benninger RK, Purbhoo MA, Sowinski S, Hume AN, et al. Structurally distinct membrane nanotubes between human macrophages support long-distance vesicular traffic or surfing of bacteria. J Immunol. 2006;177(12):8476–8483. doi: 10.4049/jimmunol.177.12.8476. PubMed DOI

Yasuda K, Khandare A, Burianovskyy L, Maruyama S, Zhang F, Nasjletti A, et al. Tunneling nanotubes mediate rescue of prematurely senescent endothelial cells by endothelial progenitors: exchange of lysosomal pool. Aging (Albany NY) 2011;3(6):597–608. doi: 10.18632/aging.100341. PubMed DOI PMC

Valdinocci D, Simoes RF, Kovarova J, Cunha-Oliveira T, Neuzil J, Pountney DL. Intracellular and intercellular mitochondrial dynamics in Parkinson's disease. Front Neurosci. 2019;13:930. doi: 10.3389/fnins.2019.00930. PubMed DOI PMC

Rogers RS, Bhattacharya J. When cells become organelle donors. Physiology (Bethesda) 2013;28(6):414–422. PubMed

Wang X, Gerdes HH. Transfer of mitochondria via tunneling nanotubes rescues apoptotic PC12 cells. Cell Death Differ. 2015;22(7):1181–1191. doi: 10.1038/cdd.2014.211. PubMed DOI PMC

Gousset K, Schiff E, Langevin C, Marijanovic Z, Caputo A, Browman DT, et al. Prions hijack tunnelling nanotubes for intercellular spread. Nat Cell Biol. 2009;11(3):328–336. doi: 10.1038/ncb1841. PubMed DOI

Dubey GP, Ben-Yehuda S. Intercellular nanotubes mediate bacterial communication. Cell. 2011;144(4):590–600. doi: 10.1016/j.cell.2011.01.015. PubMed DOI

Sowinski S, Jolly C, Berninghausen O, Purbhoo MA, Chauveau A, Kohler K, et al. Membrane nanotubes physically connect T cells over long distances presenting a novel route for HIV-1 transmission. Nat Cell Biol. 2008;10(2):211–219. doi: 10.1038/ncb1682. PubMed DOI

Okafo G, Prevedel L, Eugenin E. Tunneling nanotubes (TNT) mediate long-range gap junctional communication: Implications for HIV cell to cell spread. Sci Rep. 2017;7(1):16660. doi: 10.1038/s41598-017-16600-1. PubMed DOI PMC

Jansens RJJ, Tishchenko A, Favoreel HW. Bridging the gap: virus long-distance spread via tunneling nanotubes. J Virol. 2020;94(8):e02120-19. doi: 10.1128/JVI.02120-19. PubMed DOI PMC

Roberts KL, Manicassamy B, Lamb RA. Influenza A virus uses intercellular connections to spread to neighboring cells. J Virol. 2015;89(3):1537–1549. doi: 10.1128/JVI.03306-14. PubMed DOI PMC

Van den Broeke C, Radu M, Deruelle M, Nauwynck H, Hofmann C, Jaffer ZM, et al. Alphaherpesvirus US3-mediated reorganization of the actin cytoskeleton is mediated by group A p21-activated kinases. Proc Natl Acad Sci USA. 2009;106(21):8707–8712. doi: 10.1073/pnas.0900436106. PubMed DOI PMC

Panasiuk M, Rychlowski M, Derewonko N, Bienkowska-Szewczyk K. Tunneling nanotubes as a novel route of cell-to-cell spread of herpesviruses. J Virol. 2018;92(10):e00090-18. doi: 10.1128/JVI.00090-18. PubMed DOI PMC

Omsland M, Pise-Masison C, Fujikawa D, Galli V, Fenizia C, Parks RW, et al. Inhibition of tunneling nanotube (TNT) formation and human T-cell leukemia virus type 1 (HTLV-1) transmission by cytarabine. Sci Rep. 2018;8(1):11118. doi: 10.1038/s41598-018-29391-w. PubMed DOI PMC

Abounit S, Bousset L, Loria F, Zhu S, de Chaumont F, Pieri L, et al. Tunneling nanotubes spread fibrillar alpha-synuclein by intercellular trafficking of lysosomes. EMBO J. 2016;35(19):2120–2138. doi: 10.15252/embj.201593411. PubMed DOI PMC

Dieriks BV, Park TI, Fourie C, Faull RL, Dragunow M, Curtis MA. Alpha-synuclein transfer through tunneling nanotubes occurs in SH-SY5Y cells and primary brain pericytes from Parkinson's disease patients. Sci Rep. 2017;7:42984. doi: 10.1038/srep42984. PubMed DOI PMC

Clavaguera F, Bolmont T, Crowther RA, Abramowski D, Frank S, Probst A, et al. Transmission and spreading of tauopathy in transgenic mouse brain. Nat Cell Biol. 2009;11(7):909–913. doi: 10.1038/ncb1901. PubMed DOI PMC

Tardivel M, Begard S, Bousset L, Dujardin S, Coens A, Melki R, et al. Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies. Acta Neuropathol Commun. 2016;4(1):117. doi: 10.1186/s40478-016-0386-4. PubMed DOI PMC

Dilna A, Deepak KV, Damodaran N, Kielkopf CS, Kagedal K, Ollinger K, et al. Amyloid-beta induced membrane damage instigates tunneling nanotube-like conduits by p21-activated kinase dependent actin remodulation. Biochim Biophys Acta Mol Basis Dis. 2021;1867(12):166246. doi: 10.1016/j.bbadis.2021.166246. PubMed DOI

Costanzo M, Abounit S, Marzo L, Danckaert A, Chamoun Z, Roux P, et al. Transfer of polyglutamine aggregates in neuronal cells occurs in tunneling nanotubes. J Cell Sci. 2013;126(Pt 16):3678–3685. PubMed

Domert J, Rao SB, Agholme L, Brorsson AC, Marcusson J, Hallbeck M, et al. Spreading of amyloid-beta peptides via neuritic cell-to-cell transfer is dependent on insufficient cellular clearance. Neurobiol Dis. 2014;65:82–92. doi: 10.1016/j.nbd.2013.12.019. PubMed DOI

Nath S, Agholme L, Kurudenkandy FR, Granseth B, Marcusson J, Hallbeck M. Spreading of neurodegenerative pathology via neuron-to-neuron transmission of beta-amyloid. J Neurosci. 2012;32(26):8767–8777. doi: 10.1523/JNEUROSCI.0615-12.2012. PubMed DOI PMC

Sahu P, Jena SR, Samanta L. Tunneling nanotubes: a versatile target for cancer therapy. Curr Cancer Drug Targets. 2018;18(6):514–521. doi: 10.2174/1568009618666171129222637. PubMed DOI

Hekmatshoar Y, Nakhle J, Galloni M, Vignais ML. The role of metabolism and tunneling nanotube-mediated intercellular mitochondria exchange in cancer drug resistance. Biochem J. 2018;475(14):2305–2328. doi: 10.1042/BCJ20170712. PubMed DOI

Lou E, Fujisawa S, Morozov A, Barlas A, Romin Y, Dogan Y, et al. Tunneling nanotubes provide a unique conduit for intercellular transfer of cellular contents in human malignant pleural mesothelioma. PLoS One. 2012;7(3):e33093. doi: 10.1371/journal.pone.0033093. PubMed DOI PMC

Osswald M, Jung E, Sahm F, Solecki G, Venkataramani V, Blaes J, et al. Brain tumour cells interconnect to a functional and resistant network. Nature. 2015;528(7580):93–98. doi: 10.1038/nature16071. PubMed DOI

Salaud C, Alvarez-Arenas A, Geraldo F, Belmonte-Beitia J, Calvo GF, Gratas C, et al. Mitochondria transfer from tumor-activated stromal cells (TASC) to primary glioblastoma cells. Biochem Biophys Res Commun. 2020;533(1):139–147. doi: 10.1016/j.bbrc.2020.08.101. PubMed DOI

Pinto G, Brou C, Zurzolo C. Tunneling nanotubes: the fuel of tumor progression? Trends Cancer. 2020;6(10):874–888. doi: 10.1016/j.trecan.2020.04.012. PubMed DOI

Marlein CR, Piddock RE, Mistry JJ, Zaitseva L, Hellmich C, Horton RH, et al. CD38-driven mitochondrial trafficking promotes bioenergetic plasticity in multiple myeloma. Cancer Res. 2019;79(9):2285–2297. doi: 10.1158/0008-5472.CAN-18-0773. PubMed DOI

Lou E, Zhai E, Sarkari A, Desir S, Wong P, Iizuka Y, et al. Cellular and molecular networking within the ecosystem of cancer cell communication via tunneling nanotubes. Front Cell Dev Biol. 2018;6:95. doi: 10.3389/fcell.2018.00095. PubMed DOI PMC

Mattson MP, Culmsee C, Yu ZF. Apoptotic and antiapoptotic mechanisms in stroke. Cell Tissue Res. 2000;301(1):173–187. doi: 10.1007/s004419900154. PubMed DOI

Ham PB, 3rd, Raju R. Mitochondrial function in hypoxic ischemic injury and influence of aging. Prog Neurobiol. 2017;157:92–116. doi: 10.1016/j.pneurobio.2016.06.006. PubMed DOI PMC

Perillo B, Di Donato M, Pezone A, Di Zazzo E, Giovannelli P, Galasso G, et al. ROS in cancer therapy: the bright side of the moon. Exp Mol Med. 2020;52(2):192–203. doi: 10.1038/s12276-020-0384-2. PubMed DOI PMC

Rustom A. The missing link: does tunnelling nanotube-based supercellularity provide a new understanding of chronic and lifestyle diseases? Open Biol. 2016;6(6):160057. doi: 10.1098/rsob.160057. PubMed DOI PMC

Desir S, Wong P, Turbyville T, Chen D, Shetty M, Clark C, et al. Intercellular transfer of oncogenic KRAS via tunneling nanotubes introduces intracellular mutational heterogeneity in colon cancer cells. Cancers (Basel) 2019;11(7):892. doi: 10.3390/cancers11070892. PubMed DOI PMC

Pinto G, Saenz-de-Santa-Maria I, Chastagner P, Perthame E, Delmas C, Toulas C, et al. Patient-derived glioblastoma stem cells transfer mitochondria through tunneling nanotubes in tumor organoids. Biochem J. 2021;478(1):21–39. doi: 10.1042/BCJ20200710. PubMed DOI PMC

Ma L, Weinberg RA. Micromanagers of malignancy: role of microRNAs in regulating metastasis. Trends Genet. 2008;24(9):448–456. doi: 10.1016/j.tig.2008.06.004. PubMed DOI

Ma L, Teruya-Feldstein J, Weinberg RA. Tumour invasion and metastasis initiated by microRNA-10b in breast cancer. Nature. 2007;449(7163):682–688. doi: 10.1038/nature06174. PubMed DOI

Boukelmoune N, Chiu GS, Kavelaars A, Heijnen CJ. Mitochondrial transfer from mesenchymal stem cells to neural stem cells protects against the neurotoxic effects of cisplatin. Acta Neuropathol Commun. 2018;6(1):139. doi: 10.1186/s40478-018-0644-8. PubMed DOI PMC

Diaz-Carballo D, Klein J, Acikelli AH, Wilk C, Saka S, Jastrow H, et al. Cytotoxic stress induces transfer of mitochondria-associated human endogenous retroviral RNA and proteins between cancer cells. Oncotarget. 2017;8(56):95945–95964. doi: 10.18632/oncotarget.21606. PubMed DOI PMC

Marlein CR, Zaitseva L, Piddock RE, Robinson SD, Edwards DR, Shafat MS, et al. NADPH oxidase-2 derived superoxide drives mitochondrial transfer from bone marrow stromal cells to leukemic blasts. Blood. 2017;130(14):1649–1660. doi: 10.1182/blood-2017-03-772939. PubMed DOI

Ippolito L, Morandi A, Taddei ML, Parri M, Comito G, Iscaro A, et al. Cancer-associated fibroblasts promote prostate cancer malignancy via metabolic rewiring and mitochondrial transfer. Oncogene. 2019;38(27):5339–5355. doi: 10.1038/s41388-019-0805-7. PubMed DOI

Pasquier J, Guerrouahen BS, Al Thawadi H, Ghiabi P, Maleki M, Abu-Kaoud N, et al. Preferential transfer of mitochondria from endothelial to cancer cells through tunneling nanotubes modulates chemoresistance. J Transl Med. 2013;11:94. doi: 10.1186/1479-5876-11-94. PubMed DOI PMC

Lu J, Zheng X, Li F, Yu Y, Chen Z, Liu Z, et al. Tunneling nanotubes promote intercellular mitochondria transfer followed by increased invasiveness in bladder cancer cells. Oncotarget. 2017;8(9):15539–15552. doi: 10.18632/oncotarget.14695. PubMed DOI PMC

Burt R, Dey A, Aref S, Aguiar M, Akarca A, Bailey K, et al. Activated stromal cells transfer mitochondria to rescue acute lymphoblastic leukemia cells from oxidative stress. Blood. 2019;134(17):1415–1429. doi: 10.1182/blood.2019001398. PubMed DOI PMC

Wang J, Liu X, Qiu Y, Shi Y, Cai J, Wang B, et al. Cell adhesion-mediated mitochondria transfer contributes to mesenchymal stem cell-induced chemoresistance on T cell acute lymphoblastic leukemia cells. J Hematol Oncol. 2018;11(1):11. doi: 10.1186/s13045-018-0554-z. PubMed DOI PMC

Lin HY, Liou CW, Chen SD, Hsu TY, Chuang JH, Wang PW, et al. Mitochondrial transfer from Wharton's jelly-derived mesenchymal stem cells to mitochondria-defective cells recaptures impaired mitochondrial function. Mitochondrion. 2015;22:31–44. doi: 10.1016/j.mito.2015.02.006. PubMed DOI

Walters HE, Cox LS. Intercellular transfer of mitochondria between senescent cells through cytoskeleton-supported intercellular bridges requires mTOR and CDC42 signalling. Oxid Med Cell Longev. 2021;2021:6697861. doi: 10.1155/2021/6697861. PubMed DOI PMC

Desir S, Dickson EL, Vogel RI, Thayanithy V, Wong P, Teoh D, et al. Tunneling nanotube formation is stimulated by hypoxia in ovarian cancer cells. Oncotarget. 2016;7(28):43150–43161. doi: 10.18632/oncotarget.9504. PubMed DOI PMC

Vidulescu C, Clejan S, O'Connor KC. Vesicle traffic through intercellular bridges in DU 145 human prostate cancer cells. J Cell Mol Med. 2004;8(3):388–396. doi: 10.1111/j.1582-4934.2004.tb00328.x. PubMed DOI PMC

Valdebenito S, Audia A, Bhat KPL, Okafo G, Eugenin EA. Tunneling nanotubes mediate adaptation of glioblastoma cells to temozolomide and ionizing radiation treatment. iScience. 2020;23(9):101450. doi: 10.1016/j.isci.2020.101450. PubMed DOI PMC

Matejka N, Reindl J. Influence of alpha-particle radiation on intercellular communication networks of tunneling nanotubes in U87 glioblastoma cells. Front Oncol. 2020;10:1691. doi: 10.3389/fonc.2020.01691. PubMed DOI PMC

Polak R, de Rooij B, Pieters R, den Boer ML. B-cell precursor acute lymphoblastic leukemia cells use tunneling nanotubes to orchestrate their microenvironment. Blood. 2015;126(21):2404–2414. doi: 10.1182/blood-2015-03-634238. PubMed DOI

Desir S, O'Hare P, Vogel RI, Sperduto W, Sarkari A, Dickson EL, et al. Chemotherapy-induced tunneling nanotubes mediate intercellular drug efflux in pancreatic cancer. Sci Rep. 2018;8(1):9484. doi: 10.1038/s41598-018-27649-x. PubMed DOI PMC

Kolba MD, Dudka W, Zaręba-Kozioł M, Kominek A, Ronchi P, Turos L, et al. Tunneling nanotube-mediated intercellular vesicle and protein transfer in the stroma-provided imatinib resistance in chronic myeloid leukemia cells. Cell Death Dis. 2019;10(11):817. doi: 10.1038/s41419-019-2045-8. PubMed DOI PMC

Torralba D, Baixauli F, Sanchez-Madrid F. Mitochondria know no boundaries: mechanisms and functions of intercellular mitochondrial transfer. Front Cell Dev Biol. 2016;4:107. doi: 10.3389/fcell.2016.00107. PubMed DOI PMC

Brandon MC, Lott MT, Nguyen KC, Spolim S, Navathe SB, Baldi P, et al. MITOMAP: a human mitochondrial genome database—2004 update. Nucleic Acids Res. 2005;33(Database issue):D611–D613. doi: 10.1093/nar/gki079. PubMed DOI PMC

Mason PA, Matheson EC, Hall AG, Lightowlers RN. Mismatch repair activity in mammalian mitochondria. Nucleic Acids Res. 2003;31(3):1052–1058. doi: 10.1093/nar/gkg167. PubMed DOI PMC

Shanmughapriya S, Langford D, Natarajaseenivasan K. Inter and intracellular mitochondrial trafficking in health and disease. Ageing Res Rev. 2020;62:101128. doi: 10.1016/j.arr.2020.101128. PubMed DOI PMC

Liu K, Ji K, Guo L, Wu W, Lu H, Shan P, et al. Mesenchymal stem cells rescue injured endothelial cells in an in vitro ischemia-reperfusion model via tunneling nanotube like structure-mediated mitochondrial transfer. Microvasc Res. 2014;92:10–18. doi: 10.1016/j.mvr.2014.01.008. PubMed DOI

Dong LF, Kovarova J, Bajzikova M, Bezawork-Geleta A, Svec D, Endaya B, et al. Horizontal transfer of whole mitochondria restores tumorigenic potential in mitochondrial DNA-deficient cancer cells. Elife. 2017;6:e22187. doi: 10.7554/eLife.22187. PubMed DOI PMC

Sarmah D, Kaur H, Saraf J, Pravalika K, Goswami A, Kalia K, et al. Getting closer to an effective intervention of ischemic stroke: the big promise of stem cell. Transl Stroke Res. 2018;9(4):356–374. doi: 10.1007/s12975-017-0580-0. PubMed DOI

Islam MN, Das SR, Emin MT, Wei M, Sun L, Westphalen K, et al. Mitochondrial transfer from bone-marrow-derived stromal cells to pulmonary alveoli protects against acute lung injury. Nat Med. 2012;18(5):759–765. doi: 10.1038/nm.2736. PubMed DOI PMC

Paliwal S, Chaudhuri R, Agrawal A, Mohanty S. Regenerative abilities of mesenchymal stem cells through mitochondrial transfer. J Biomed Sci. 2018;25(1):31. doi: 10.1186/s12929-018-0429-1. PubMed DOI PMC

Hayakawa K, Esposito E, Wang X, Terasaki Y, Liu Y, Xing C, et al. Transfer of mitochondria from astrocytes to neurons after stroke. Nature. 2016;535(7613):551–555. doi: 10.1038/nature18928. PubMed DOI PMC

Yao Y, Fan XL, Jiang D, Zhang Y, Li X, Xu ZB, et al. Connexin 43-mediated mitochondrial transfer of iPSC-MSCs alleviates asthma inflammation. Stem Cell Rep. 2018;11(5):1120–1135. doi: 10.1016/j.stemcr.2018.09.012. PubMed DOI PMC

Jiang D, Chen FX, Zhou H, Lu YY, Tan H, Yu SJ, et al. Bioenergetic crosstalk between mesenchymal stem cells and various ocular cells through the intercellular trafficking of mitochondria. Theranostics. 2020;10(16):7260–7272. doi: 10.7150/thno.46332. PubMed DOI PMC

Mahrouf-Yorgov M, Augeul L, Da Silva CC, Jourdan M, Rigolet M, Manin S, et al. Mesenchymal stem cells sense mitochondria released from damaged cells as danger signals to activate their rescue properties. Cell Death Differ. 2017;24(7):1224–1238. doi: 10.1038/cdd.2017.51. PubMed DOI PMC

Li CJ, Chen PK, Sun LY, Pang CY. Enhancement of mitochondrial transfer by antioxidants in human mesenchymal stem cells. Oxid Med Cell Longev. 2017;2017:8510805. doi: 10.1155/2017/8510805. PubMed DOI PMC

Han H, Hu J, Yan Q, Zhu J, Zhu Z, Chen Y, et al. Bone marrow-derived mesenchymal stem cells rescue injured H9c2 cells via transferring intact mitochondria through tunneling nanotubes in an in vitro simulated ischemia/reperfusion model. Mol Med Rep. 2016;13(2):1517–1524. doi: 10.3892/mmr.2015.4726. PubMed DOI PMC

Lin TK, Chen SD, Chuang YC, Lan MY, Chuang JH, Wang PW, et al. Mitochondrial transfer of Wharton's jelly mesenchymal stem cells eliminates mutation burden and rescues mitochondrial bioenergetics in rotenone-stressed MELAS fibroblasts. Oxid Med Cell Longev. 2019;2019:9537504. doi: 10.1155/2019/9537504. PubMed DOI PMC

Chuang YC, Liou CW, Chen SD, Wang PW, Chuang JH, Tiao MM, et al. Mitochondrial transfer from Wharton's jelly mesenchymal stem cell to MERRF cybrid reduces oxidative stress and improves mitochondrial bioenergetics. Oxid Med Cell Longev. 2017;2017:5691215. doi: 10.1155/2017/5691215. PubMed DOI PMC

Jiang D, Gao F, Zhang Y, Wong DS, Li Q, Tse HF, et al. Mitochondrial transfer of mesenchymal stem cells effectively protects corneal epithelial cells from mitochondrial damage. Cell Death Dis. 2016;7(11):e2467. doi: 10.1038/cddis.2016.358. PubMed DOI PMC

Yang Y, Ye G, Zhang YL, He HW, Yu BQ, Hong YM, et al. Transfer of mitochondria from mesenchymal stem cells derived from induced pluripotent stem cells attenuates hypoxia-ischemia-induced mitochondrial dysfunction in PC12 cells. Neural Regen Res. 2020;15(3):464–472. doi: 10.4103/1673-5374.266058. PubMed DOI PMC

Plotnikov EY, Khryapenkova TG, Galkina SI, Sukhikh GT, Zorov DB. Cytoplasm and organelle transfer between mesenchymal multipotent stromal cells and renal tubular cells in co-culture. Exp Cell Res. 2010;316(15):2447–2455. doi: 10.1016/j.yexcr.2010.06.009. PubMed DOI

Vallabhaneni KC, Haller H, Dumler I. Vascular smooth muscle cells initiate proliferation of mesenchymal stem cells by mitochondrial transfer via tunneling nanotubes. Stem Cells Dev. 2012;21(17):3104–3113. doi: 10.1089/scd.2011.0691. PubMed DOI PMC

Hu J, Deng G, Tian Y, Pu Y, Cao P, Yuan W. An in vitro investigation into the role of bone marrowderived mesenchymal stem cells in the control of disc degeneration. Mol Med Rep. 2015;12(4):5701–5708. doi: 10.3892/mmr.2015.4139. PubMed DOI PMC

Babenko VA, Silachev DN, Zorova LD, Pevzner IB, Khutornenko AA, Plotnikov EY, et al. Improving the post-stroke therapeutic potency of mesenchymal multipotent stromal cells by cocultivation with cortical neurons: the role of crosstalk between cells. Stem Cells Transl Med. 2015;4(9):1011–1020. doi: 10.5966/sctm.2015-0010. PubMed DOI PMC

Babenko VA, Silachev DN, Popkov VA, Zorova LD, Pevzner IB, Plotnikov EY, et al. Miro1 enhances mitochondria transfer from multipotent mesenchymal stem cells (MMSC) to neural cells and improves the efficacy of cell recovery. Molecules. 2018;23(3):687. doi: 10.3390/molecules23030687. PubMed DOI PMC

Li H, Wang C, He T, Zhao T, Chen YY, Shen YL, et al. Mitochondrial transfer from bone marrow mesenchymal stem cells to motor neurons in spinal cord injury rats via Gap Junction. Theranostics. 2019;9(7):2017–2035. doi: 10.7150/thno.29400. PubMed DOI PMC

Jackson MV, Krasnodembskaya AD. Analysis of mitochondrial transfer in direct co-cultures of human monocyte-derived macrophages (MDM) and mesenchymal stem cells (MSC) Bio Protoc. 2017;7(9):e2255. doi: 10.21769/BioProtoc.2255. PubMed DOI PMC

Jackson MV, Morrison TJ, Doherty DF, McAuley DF, Matthay MA, Kissenpfennig A, et al. Mitochondrial transfer via tunneling nanotubes is an important mechanism by which mesenchymal stem cells enhance macrophage phagocytosis in the in vitro and in vivo models of ARDS. Stem Cells. 2016;34(8):2210–2223. doi: 10.1002/stem.2372. PubMed DOI PMC

Cselenyak A, Pankotai E, Horvath EM, Kiss L, Lacza Z. Mesenchymal stem cells rescue cardiomyoblasts from cell death in an in vitro ischemia model via direct cell-to-cell connections. BMC Cell Biol. 2010;11:29. doi: 10.1186/1471-2121-11-29. PubMed DOI PMC

Yang H, Borg TK, Ma Z, Xu M, Wetzel G, Saraf LV, et al. Biochip-based study of unidirectional mitochondrial transfer from stem cells to myocytes via tunneling nanotubes. Biofabrication. 2016;8(1):015012. doi: 10.1088/1758-5090/8/1/015012. PubMed DOI

Zhang Y, Yu Z, Jiang D, Liang X, Liao S, Zhang Z, et al. iPSC-MSCs with High intrinsic MIRO1 and sensitivity to TNF-alpha yield efficacious mitochondrial transfer to rescue anthracycline-induced cardiomyopathy. Stem Cell Rep. 2016;7(4):749–763. doi: 10.1016/j.stemcr.2016.08.009. PubMed DOI PMC

Li X, Zhang Y, Yeung SC, Liang Y, Liang X, Ding Y, et al. Mitochondrial transfer of induced pluripotent stem cell-derived mesenchymal stem cells to airway epithelial cells attenuates cigarette smoke-induced damage. Am J Respir Cell Mol Biol. 2014;51(3):455–465. doi: 10.1165/rcmb.2013-0529OC. PubMed DOI

Paliwal S, Chaudhuri R, Agrawal A, Mohanty S. Correction to: Human tissue-specific MSCs demonstrate differential mitochondria transfer abilities that may determine their regenerative abilities. Stem Cell Res Ther. 2019;10(1):215. doi: 10.1186/s13287-019-1343-5. PubMed DOI PMC

Tan AS, Baty JW, Dong LF, Bezawork-Geleta A, Endaya B, Goodwin J, et al. Mitochondrial genome acquisition restores respiratory function and tumorigenic potential of cancer cells without mitochondrial DNA. Cell Metab. 2015;21(1):81–94. doi: 10.1016/j.cmet.2014.12.003. PubMed DOI

Wallace DC. Mitochondrial DNA sequence variation in human evolution and disease. Proc Natl Acad Sci USA. 1994;91(19):8739–8746. doi: 10.1073/pnas.91.19.8739. PubMed DOI PMC

Bajzikova M, Kovarova J, Coelho AR, Boukalova S, Oh S, Rohlenova K, et al. Reactivation of dihydroorotate dehydrogenase-driven pyrimidine biosynthesis restores tumor growth of respiration-deficient cancer cells. Cell Metab. 2019;29(2):399–416 e10. doi: 10.1016/j.cmet.2018.10.014. PubMed DOI PMC

Andresen V, Wang X, Ghimire S, Omsland M, Gjertsen BT, Gerdes HH. Tunneling nanotube (TNT) formation is independent of p53 expression. Cell Death Differ. 2013;20(8):1124. doi: 10.1038/cdd.2013.61. PubMed DOI PMC

Scheiblich H, Dansokho C, Mercan D, Schmidt SV, Bousset L, Wischhof L, et al. Microglia jointly degrade fibrillar alpha-synuclein cargo by distribution through tunneling nanotubes. Cell. 2021;184(20):5089–5106 e21. doi: 10.1016/j.cell.2021.09.007. PubMed DOI PMC

Austefjord MW, Gerdes HH, Wang X. Tunneling nanotubes: diversity in morphology and structure. Commun Integr Biol. 2014;7(1):e27934. doi: 10.4161/cib.27934. PubMed DOI PMC

Hanna SJ, McCoy-Simandle K, Miskolci V, Guo P, Cammer M, Hodgson L, et al. The role of Rho-GTPases and actin polymerization during macrophage tunneling nanotube biogenesis. Sci Rep. 2017;7(1):8547. doi: 10.1038/s41598-017-08950-7. PubMed DOI PMC

Rangamani P, Levy MG, Khan S, Oster G. Paradoxical signaling regulates structural plasticity in dendritic spines. Proc Natl Acad Sci USA. 2016;113(36):E5298–E5307. doi: 10.1073/pnas.1610391113. PubMed DOI PMC

Vargas JY, Loria F, Wu YJ, Cordova G, Nonaka T, Bellow S, et al. The Wnt/Ca(2+) pathway is involved in interneuronal communication mediated by tunneling nanotubes. EMBO J. 2019;38(23):e101230. doi: 10.15252/embj.2018101230. PubMed DOI PMC

Shen K, Meyer T. Dynamic control of CaMKII translocation and localization in hippocampal neurons by NMDA receptor stimulation. Science. 1999;284(5411):162–166. doi: 10.1126/science.284.5411.162. PubMed DOI

Dagar S, Pushpa K, Pathak D, Samaddar S, Saxena A, Banerjee S, et al. Nucleolin regulates 14-3-3zeta mRNA and promotes cofilin phosphorylation to induce tunneling nanotube formation. FASEB J. 2021;35(1):e21199. doi: 10.1096/fj.202001152R. PubMed DOI

Jacob T, Broeke CVD, Waesberghe CV, Troys LV, Favoreel HW. Pseudorabies virus US3 triggers RhoA phosphorylation to reorganize the actin cytoskeleton. J Gen Virol. 2015;96(8):2328–2335. doi: 10.1099/vir.0.000152. PubMed DOI

Mukerji J, Olivieri KC, Misra V, Agopian KA, Gabuzda D. Proteomic analysis of HIV-1 Nef cellular binding partners reveals a role for exocyst complex proteins in mediating enhancement of intercellular nanotube formation. Retrovirology. 2012;9:33. doi: 10.1186/1742-4690-9-33. PubMed DOI PMC

Delage E, Cervantes DC, Penard E, Schmitt C, Syan S, Disanza A, et al. Differential identity of filopodia and tunneling nanotubes revealed by the opposite functions of actin regulatory complexes. Sci Rep. 2016;6:39632. doi: 10.1038/srep39632. PubMed DOI PMC

Las G, Shirihai OS. Miro1: new wheels for transferring mitochondria. EMBO J. 2014;33(9):939–941. doi: 10.1002/embj.201488441. PubMed DOI PMC

Wang F, Chen X, Cheng H, Song L, Liu J, Caplan S, et al. MICAL2PV suppresses the formation of tunneling nanotubes and modulates mitochondrial trafficking. EMBO Rep. 2021;22(7):e52006. doi: 10.15252/embr.202052006. PubMed DOI PMC

Ridley AJ. Rho GTPases and actin dynamics in membrane protrusions and vesicle trafficking. Trends Cell Biol. 2006;16(10):522–529. doi: 10.1016/j.tcb.2006.08.006. PubMed DOI

Hase K, Kimura S, Takatsu H, Ohmae M, Kawano S, Kitamura H, et al. M-Sec promotes membrane nanotube formation by interacting with Ral and the exocyst complex. Nat Cell Biol. 2009;11(12):1427–1432. doi: 10.1038/ncb1990. PubMed DOI

Bhat S, Ljubojevic N, Zhu S, Fukuda M, Echard A, Zurzolo C. Rab35 and its effectors promote formation of tunneling nanotubes in neuronal cells. Sci Rep. 2020;10(1):16803. doi: 10.1038/s41598-020-74013-z. PubMed DOI PMC

Burtey A, Wagner M, Hodneland E, Skaftnesmo KO, Schoelermann J, Mondragon IR, et al. Intercellular transfer of transferrin receptor by a contact-, Rab8-dependent mechanism involving tunneling nanotubes. FASEB J. 2015;29(11):4695–4712. doi: 10.1096/fj.14-268615. PubMed DOI

Aznar S, Lacal JC. Rho signals to cell growth and apoptosis. Cancer Lett. 2001;165(1):1–10. doi: 10.1016/S0304-3835(01)00412-8. PubMed DOI

Ozaki M, Deshpande SS, Angkeow P, Bellan J, Lowenstein CJ, Dinauer MC, et al. Inhibition of the Rac1 GTPase protects against nonlethal ischemia/reperfusion-induced necrosis and apoptosis in vivo. FASEB J. 2000;14(2):418–429. doi: 10.1096/fasebj.14.2.418. PubMed DOI

Lin L, Zhang M, Stoilov P, Chen L, Zheng S. Developmental attenuation of neuronal apoptosis by neural-specific splicing of Bak1 microexon. Neuron. 2020;107(6):1180–1196 e8. doi: 10.1016/j.neuron.2020.06.036. PubMed DOI PMC

Stankiewicz TR, Linseman DA. Rho family GTPases: key players in neuronal development, neuronal survival, and neurodegeneration. Front Cell Neurosci. 2014;8:314. doi: 10.3389/fncel.2014.00314. PubMed DOI PMC

Cole JM, Dahl R, Cowden Dahl KD. MAPK signaling is required for generation of tunneling nanotube-like structures in ovarian cancer cells. Cancers (Basel) 2021;13(2):274. doi: 10.3390/cancers13020274. PubMed DOI PMC

Arkwright PD, Luchetti F, Tour J, Roberts C, Ayub R, Morales AP, et al. Fas stimulation of T lymphocytes promotes rapid intercellular exchange of death signals via membrane nanotubes. Cell Res. 2010;20(1):72–88. doi: 10.1038/cr.2009.112. PubMed DOI PMC

Luchetti F, Canonico B, Arcangeletti M, Guescini M, Cesarini E, Stocchi V, et al. Fas signalling promotes intercellular communication in T cells. PLoS One. 2012;7(4):e35766. doi: 10.1371/journal.pone.0035766. PubMed DOI PMC

Levoux J, Prola A, Lafuste P, Gervais M, Chevallier N, Koumaiha Z, et al. Platelets facilitate the wound-healing capability of mesenchymal stem cells by mitochondrial transfer and metabolic reprogramming. Cell Metab. 2021;33(3):688–690. doi: 10.1016/j.cmet.2021.02.003. PubMed DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...