F-actin bundles are derivatives of microvilli: What does this tell us about how bundles might form?

Journal of Cell Biology

Volumn 148, Issue 1, 2000, Pages 1-6

  DeRosier, David J ^a   Tilney, Lewis G ^b  

^a BRANDEIS UNIVERSITY   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; PHALLOIDIN;

BRUSH BORDER; CONFOCAL MICROSCOPY; DROSOPHILA; MICROVILLUS; PRIORITY JOURNAL; SEA URCHIN; SHORT SURVEY;

ACTINS; ANIMALS; DROSOPHILA MELANOGASTER; HUMANS; MICROVILLI;

ECHINOIDEA;

EID: 0034627754     PISSN: 00219525     EISSN: None     Source Type: Journal    
DOI: 10.1083/jcb.148.1.1     Document Type: Short Survey

References (25)

1. Bartles, J.R., L. Zheng, A. Li, A. Wierda, and B. Chen. 1998. Small espin: a third actin-bundling protein and potential forked protein ortholog in brush border microvilli. J. Cell Biol. 143:107-119.
2. Beckerle, M.C. 1998. Spatial control of actin filament assembly: lessons from Listeria. Cell. 95:741-748.
3. Begg, D.A., L.I. Rebhun, and H. Hyatt. 1982. Structural organization of aetin in the sea urchin egg cortex: microvillar elongation in the absence of actin filament bundle formation. J. Cell Biol. 93:24-32.
4. Duda, R.L., and F.A. Eiserling. 1982. Evidence for an internal component of the bacteriophage T4D tail core: a possible length-determining template. J. Virol. 43:714-720.
5. Ezzell, R.M., M.M. Chafel, and P.T. Matsudaira. 1989. Differential localization of villin and fimbrin during development of the mouse visceral endoderm and intestinal epithelium. Development. 106:407-419.
6. Fath, K.R., S.D. Obenauf, and D.R. Burgess. 1990. Cytoskeletal protein and mRNA accumulation during brush border formation in adult chicken enterocytes. Development. 109:449-459.
7. 2+-dependent F-actin disruption in intestinal brush borders. J. Cell Biol. 146:819-829.
8. Guild, G.M., P.S. Connelly, M.K. Shaw, and L.G. Tilney. 1997. Actin filament cables in Drosophila nurse cells are composed of modules that slide passively past one another during dumping. J. Cell Biol. 138:783-797.
9. Kruger, M., J. Wright, and K. Wang. 1991. Nebulin as a length regulator of thin filaments of vertebrate skeletal muscles: correlation of thin filament length, nebulin size, and epitope profile. J. Cell Biol. 115:97-107.
10. Machesky, L.M., and R.H. Insall. 1999. Signalling to actin dynamics. J. Cell Biol. 146:267-272.
11. Mullins, R.D., J.A. Heuser, and T.D. Pollard. 1998. The interaction of Arp2/3 complex with actin: nucleation, high affinity pointed end capping, and formation of branching networks of filaments. Proc. Natl. Acad. Sci. USA. 95: 6181-6186.
12. Mullins, R.D., W.F. Stafford, and T.D. Pollard. 1997. Structure, subunit topology, and actin-binding activity of the Arp2/3 complex from Acanthamoeba. J. Cell Biol. 136:331-343.
13. Shibayama, T., J.M. Carboni, and M.S. Mooseker. 1987. Assembly of the intestinal brush border: appearance and redistribution of microvillar core proteins in developing chick enterocytes. J. Cell Biol. 105:335-344.
14. Stokes, D.L., and D.J. DeRosier. 1991. Growth conditions control the size and order of actin bundles in vitro. Biophys. J. 59:456-465.
15. Svitkina, T.M., and G.G. Borisy. 1999. Arp2/3 complex and actin depolymerizing factor/cofilin in dendritic organization and treadmilling of actin filament array in lamellipodia. J. Cell Biol. 145:1009-1026.
16. Tilney, L.G., E.M. Bonder, and D.J. DeRosier. 1981. Actin filaments elongate from their membrane-associated ends. J. Cell Biol. 90:485-494.
17. Tilney, L.G., P. Connelly, S. Smith, and G.M. Guild. 1996. F-actin bundles in Drosophila bristles are assembled from modules composed of short filaments. J. Cell Biol. 135:1291-1308.
18. Tilney, L.G., P.S. Connelly, K.A. Vranich, M.K. Shaw, and G.M. Guild. 1998. Why are two different cross-linkers necessary for actin bundle formation in vivo and what does each cross-link contribute? J. Cell Biol. 143:121-133.
19. Tilney, L.G., and D.J. DeRosier. 1986. Actin filaments, stereocilia, and hair cells of the bird cochlea. IV. How the actin filaments become organised in developing stereocilia and in the cuticular plate. Dev Biol. 116:119-129.
20. Tilney, L.G., D.J. DeRosier, A. Weber, and M.S. Tilney. 1992. How Listeria exploits host cell actin to form its own cytoskeleton. II. Nucleation, actin filament polarity, filament assembly, and evidence for a pointed end capper. J. Cell Biol. 118:83-93.
21. Tilney, L.G., E.H. Egelman, D.J. DeRosier, and J.C. Saunder. 1983. Actin filaments, stereocilia, and hair cells of the bird cochlea. II. Packing of actin filaments in the stereocilia and in the cuticular plate and what happens to the organization when the stereocilia are bent. J. Cell Biol 96:822-834.
22. Tilney, L.G., Y. Fukui, and D.J. DeRosier. 1987. Movement of the actin filament bundle in Mytilus sperm: a new mechanism is proposed. J. Cell Biol. 104:981-993.
23. Tilney, L.G., and L.A. Jaffe. 1980. Actin, microvilli, and the fertilization cone of sea urchin eggs. J. Cell Biol. 87:771-782.
24. Wachsstock, D.H., W.H. Schwartz, and T.D. Pollard. 1993. Affinity of alphaactinin for actin determines the structure and mechanical properties of actin filament gels. Biophys. J. 65:205-214.
25. Welch, M.D., A.H. DePace, S. Verma, A. Iwamatsu, and T.J. Mitchison. 1997. The human Arp2/3 complex is composed of evolutionary conserved subunits and is localized to cellular regions of dynamic actin filament assembly. J. Cell Biol. 138:375-384.