The transport along membrane nanotubes driven by the spontaneous curvature of membrane components

Bioelectrochemistry

Volumn 87, Issue , 2012, Pages 204-210

  Kabaso, Doron ^a,b   Bobrovska, Nataliya ^c   Góźdź, Wojciech ^c   Gongadze, Ekaterina ^a   Kralj Iglič, Veronika ^a   Zorec, Robert ^b,d   Iglič, Aleš ^a  

^a UNIVERSITY OF LJUBLJANA   (Slovenia)

^b UNIVERSITY OF LJUBLJANA   (Slovenia)

^c INSTITUTE OF PHYSICAL CHEMISTRY   (Poland)

^d Celica Biomedical Sciences Center   (Slovenia)

Author keywords

Computational model; Intercellular nanotubes; Membrane and cell biomechanics; Nanotube dilations (gondolas); Transport mechanism

Indexed keywords

ANISOTROPIC MEMBRANE; CHEMICAL SIGNALS; CHOLERA TOXIN B; COMPUTATIONAL MODEL; INTERCELLULAR MEMBRANES; ISOTROPIC MEMBRANE; LEADING EDGE; MEMBRANE BENDING; MEMBRANE COMPONENTS; ORIENTATIONAL ORDERINGS; SPHERICAL CELLS; SPHERICAL SHAPE; SPONTANEOUS CURVATURE; TRANSPORT MECHANISM; TRANSPORT SYSTEMS; TUBULAR SHAPES; TWO-COMPONENT; UNDERLYING MECHANISM;

ANISOTROPY; BIOMECHANICS; CELL MEMBRANES; CHOLESTEROL; COMPUTATIONAL METHODS; CYTOLOGY; EQUATIONS OF MOTION; NANOTUBES; PHOSPHOLIPIDS; SPATIAL DISTRIBUTION;

MEMBRANES;

CHOLERA TOXIN B SUBUNIT; CHOLESTEROL; NANOTUBE; SPHINGOMYELIN;

ANISOTROPY; ARTICLE; CELL MEMBRANE; COMPUTER MODEL; CURVATURE; ELECTRICITY; ENERGY; MEMBRANE COMPONENT; MEMBRANE TRANSPORT; MOTION; PHASE SEPARATION; PHYSICAL PARAMETERS;

BIOLOGICAL TRANSPORT; CELL MEMBRANE; CHOLERA TOXIN; CHOLESTEROL; ELECTRICITY; G(M1) GANGLIOSIDE; MEMBRANES, ARTIFICIAL; MODELS, CHEMICAL; MOLECULAR CONFORMATION; SPHINGOMYELINS; THERMODYNAMICS; TRANSPORT VESICLES;

EID: 84865175503     PISSN: 15675394     EISSN: 1878562X     Source Type: Journal    
DOI: 10.1016/j.bioelechem.2012.02.009     Document Type: Article

References (41)

1. Berne S., Križaj I., Pohleven F., Turk T., Maček P., Sepčič K. Pleurotus and Agrocybe hemolysins, new proteins hypothetically involved in fungal fruiting. Biochim. Biophys. Acta 2002, 1570:153-159.
2. Bukoreshtliev N.V., Wang X., Hodneland E., Gurke S., Barroso J.F., Gerdes H.H. Selective block of tunneling nanotube (TNT) formation inhibits intercellular organelle transfer between pc12 cells. FEBS Lett. 2009, 583:1481-1488.
3. Corbeil D., Röper K., Fargeas C.A., Joester A., Huttner W.B. Prominin: a story of cholesterol, plasma membrane protrusions and human pathology. Traffic 2001, 2:82-91.
4. Dommersnes P.G., Orwar O., Brochard-Wyart F., Joanny J.F. Marangoni transport in lipid nanotubes. Europhys. Lett. 2005, 70:271-277.
5. Dubey G.P., Ben-Yehuda S. Intercellular nanotubes mediate bacterial communication. Cell 2011, 144:590-600.
6. Fischer T. Bending stiffness of lipid bilayers. III. Gaussian curvature. J. Phys. II 1992, 2:337-343.
7. Fošnarič M., Bohinc K., Gauger D.R., Iglič A., Kralj-Iglič V., May S. The influence of anisotropic membrane inclusions on curvature elastic properties of lipid membranes. J. Chem. Info. Model. 2005, 45:1652-1661.
8. Gimsa U., Kralj-Iglič V., Iglič A., Fiedler S., Zwanzig M., Jonas L., Gimsa J. Basic cell-cell and cell-surface interactions in liposome and cellular systems. Advances in Planar Lipid Bilayers and Liposomes 2007, vol. 11:229-251. Elsevier, Amsterdam. A. Leitmannova Liu (Ed.).
9. Góźdź W.T. Spontaneous curvature induced shape transformations of tubular polymersomes. Langmuir 2004, 20:7385-7391.
10. Góźdź W.T. Influence of spontaneous curvature and microtubules on the conformations of lipid vesicles. J. Phys. Chem. B 2005, 109:21145-21149.
11. Góźdź W.T. The interface width of separated two-component lipid membranes. J. Phys. Chem. B 2006, 110:21981-21986.
12. Gousset K., Schiff E., Langevin C., Marijanovic Z., Caputo A., Browman D.T., Fabrice de Chaumont N.C., Martino A., Enninga J., Olivo-Marin J.C., Männel D., Zurzolo C. Prions hijack tunnelling nanotubes for intercellular spread. Nat. Cell Biol. 2009, 11:328-336.
13. Heimburg T., Jackson A.D. On soliton propagation in biomembranes and nerves. PNAS 2005, 102:9790-9795.
14. Vargas E.V., Ludu A., Hustert R., Gumrich P., Jackson A.D., Heimburg T. Periodic solutions and refractory periods in the soliton theory for nerves and the locust femoral nerve. Biophys. Chem. 2011, 153:159-167.
15. Hurtig J., Chiu T., Onfelt B. Intercellular nanotubes: insights from imaging studies and beyond. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2010, 2:260-276.
16. Iglič A., Hägerstrand H., Veranič P., Plemenitaš A., Kralj-Iglič B. Curvature induced accumulation of anisotropic membrane components 29 and raft formation in cylindrical membrane protrusions. J. Theor. Biol. 2006, 240:368-373.
17. Iglič A., Babnik B., Fošnarič M., Hägerstrand H., Kralj-Iglič V. On the role of anisotropy of membrane constituents in formation of a membrane neck during budding of multicomponent membrane. J. Biomech. 2007, 40:579-585.
18. Jorgačevski J., Fošnarič M., Vardjan N., Stenovec M., Potokar M., Kreft M., Kralj-Iglič V., Iglič A., Zorec R. Fusion pore stability of peptidergic vesicles. Mol. Membr. Biol. 2010, 27:65-80.
19. Karlsson R., Karlsson A., Orwar O. Marangoni transport in lipid nanotubes. J. Phys. Chem. B 2003, 107:11201-11207.
20. Kabaso D., Gongadze E., Perutková Š., Kralj-Iglič V., Matschegewski C., Beck U., van Rienen U., Iglič A. Mechanics and electrostatics of the interactions between osteoblasts and titanium surface. Comput. Methods Biomech. Biomed. Eng. 2011, 14:469-482.
21. Kabaso D., Gongadze E., Elter P., van Rienen K.U., Gimsa J., Iglic A. Attachment of rod-like (BAR) and membrane shape. Mini Rev. Med. Chem. 2011, 11:272-282.
22. Kabaso D., Shlomovitz R., Schloen K., Stradal T., Gov N.S. Theoretical model for cellular shapes driven by protrusive and adhesive forces. PLoS Comput. Biol. 2011, 7:1-13.
23. Kabaso D., Lokar M., Kralj-Iglic V., Veranic P., Iglic A. Temperature, cholera toxin-B and degree of malignant transformation are factors that influence formation of membrane nanotubes in urothelial cancer cell lines. Int. J. Nanomed. 2011, 6:495-509.
24. Kabaso D., Bobrovska N., Gov N.S., Kralj-Iglic V., Veranič P., Iglič A. On the role of membrane anisotropy and BAR proteins in the stability of tubular membrane structures. J. Biomech. 2012, 45:231-238.
25. Koster G., VanDuijn M., Hofs B., Dogterom M. Membrane tube formation from giant vesicles by dynamic association of motor proteins. Proc. Natl. Acad. Sci. U. S. A. 2003, 100:15583-15588.
26. Kralj-Iglič V., Heinrich V., Svetina S., Zeks B. Free energy of closed membrane with anisotropic inclusions. Eur. Phys. J. B 1999, 10:5-8.
27. Iglič A., Hägerstrand H., Bobrowska-Hägerstrand M., Arrigler V., Kralj-Iglič V. Possible role of phospholipid nanotubes in directed transport of membrane vesicles. Phys. Lett. A 2003, 310:493-497.
28. Lokar M., Iglič A., Veranič P. Protruding membrane nanotubes: attachment of tubular protrusions to adjacent cells by several anchoring junctions. Protoplasma 2010, 246:81-87.
29. Park J., Bauer S., von der Mark K., Schmuki P. Nanosize and vitality: TiO2 nanotube diameter directs cell fate. Nano Lett. 2007, 7:1686-1691.
30. Park J., Bauer S., Schmuki P., von der Mark K. Narrow window in nanoscale dependent activation of endothelial cell growth and differentiation on TiO2 nanotube surfaces. Nano Lett. 2009, 9:3157-3164.
31. Park J., Bauer S., Schlegel K.A., Neukam F.W., Mark K.V., Schmuki P. TiO2 nanotube surfaces: 15 nm-an optimal length scale of surface topography for cell adhesion and differentiation. Small 2009, 5:666-671.
32. Peter B.J., Kent H.M., Mills I.G., Vallis Y., Butler P.J., Evans P.R., McMahon H.T. BAR domains as sensors of membrane curvature: the amphiphysin BAR structure. Science 2004, 303:495-499.
33. Rustom A., Saffrich R., Markovic I., Walther P., Gerdes H. Nanotubular highways for intercellular organelle transport. Science 2004, 303:1007-1010.
34. Risselada H.J., Marrink S.J., Müller M. Curvature-dependent elastic properties of liquid-ordered domains result in inverted domain sorting on uniaxially compressed vesicles. Phys. Rev. Lett. 2011, 106:148102.
35. Sonnino S., Mauri L., Chigorno V., Prinetti A. Gangliosides as components of lipid membrane domains. Glycobiology 2006, 17:1-13.
36. Sorre B., Callan-Jones A., Manneville J.B., Nassoy P., Joanny J.F., Prost J., Goud B., Bassereau P. Curvature-driven lipid sorting needs proximity to a demixing point and is aided by proteins. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:5622-5626.
37. Tian A., Baumgart T. Sorting of lipids and proteins in membrane curvature gradients. Biophys. J. 2009, 96:2676-2688.
38. Vidulescu C., Clejan S., O'Connor K. Vesicle traffic through intercellular bridges in du 145 human prostate cancer cells. J. Cell. Mol. Med. 2004, 8:88-396.
39. Veranič P., Lokar M., Schuetz G.J., Weghuber J., Wieser S., Hagerstrand H., Kralj-Iglič V., Iglič A. Different types of cell-to-cell connections mediated by nanotubular structures. Biophys. J. 2008, 95:4416-4425.
40. Watkins S.C., Salter R.D. Functional connectivity between immune cells mediated by tunneling nanotubules. Immunity 2005, 23:309-318.
41. Weigmann A., Corbeil D., Hellwig A., Huttner W.B. Prominin, a novel microvilli-specific polytopic membrane protein of the apical surface of epithelial cells, is targeted to plasmalemmal protrusions of non-epithelial cells. Proc. Natl. Acad. Sci. U. S. A. 1997, 74:12425-12430.