Blastula wall invagination examined on the basis of shape behavior of vesicular objects with laminar envelopes

International Journal of Developmental Biology

Volumn 50, Issue 2-3, 2006, Pages 143-150

  Božič, Bojan ^a   Derganc, Jure ^a   Svetina, Saša ^a,b  

^a UNIVERSITY OF LJUBLJANA   (Slovenia)

^b JO EF STEFAN INSTITUTE   (Slovenia)

Author keywords

Epithelial sheet; Gastrulation; Laminar membrane; Shape transformation

Indexed keywords

HYALIN;

ARTICLE; BLASTULA; EMBRYO DEVELOPMENT; ERYTHROCYTE; GASTRULATION; INVAGINATION; NONHUMAN; PHOSPHOLIPID VESICLE; PRIORITY JOURNAL; SEA URCHIN;

ANIMALS; BLASTULA; GASTRULA; MODELS, BIOLOGICAL; MORPHOGENESIS;

ECHINOIDEA;

EID: 33646358738     PISSN: 02146282     EISSN: None     Source Type: Journal    
DOI: 10.1387/ijdb.052042bb     Document Type: Article

References (31)

1. BELOUSSOV, L.V. (1998). The Dynamic Architecture of a Developing Organism. An Interdisciplinary Approach to the Development of Organisms. Kluwer Academic Publishers, Dordrecht, Boston, London, pp. 1-238.
2. CANHAM, P.B. (1970). The minimum energy of bending as a possible explanation of the biconcave shape of the human red blood cell. J. Theor. Biol. 26: 61-81.
3. DAVIDSON, L.A., KOEHL, M.A.R., KELLER, R. and OSTER, G.F. (1995). How do sea urchins invaginate? Using biomechanics to distinguish between mechanisms of primary invagination. Development 121: 2005-2018.
4. DAVIDSON, L.A., OSTER, G.F., KELLER, R.E. and KOEHL, M.A.R. (1999). Measurements of mechanical properties of the blastula wall reveal which hypothesized mechanisms of primary invagination are physically plausible in the sea urchin Strongylocentrotus purpuratus. Dev. Biol. 209: 221-238.
5. DERGANC, J. (2003). Studij mehanizmov agregacije celic v linearne in dvodimenzionalne strukture. Ph.D. Thesis, University of Ljubljana.
6. DEULING, H.J. and HELFRICH, W. (1976). The curvature elasticity of fluid membranes: a catalogue of vesicle shapes. J. Phys. France 37: 1335-1345.
7. ETTENSOHN, C.A. (1985). Mechanisms of epithelial invagination. Q. Rev. Biol. 60: 289-307.
8. EVANS, E. and YEUNG, A. (1989). Apparent viscosity and cortical tension of blood granulocytes determined by micropipet aspiration. Biophys. J. 56: 151-160.
9. GUSTAFSON, T. and WOLPERT, L. (1967). Cellular movement and contact in sea urchin morphogenesis. Biol. Rev. 42: 442-498.
10. HARDIN, J. D. and CHENG, L. Y. (1986). The mechanism and mechanics of archenteron elongation during sea urchin gastrulation. Dev. Biol. 115: 490-501.
11. HEINRICH, V., SVETINA, S. and ZEKS, B. (1993). Non-axisymmetric vesicle shapes in a generalized bilayer-couple model and the transition between oblate and prolate axisymmetric shapes. Phys. Rev. E 48: 3112-3123.
12. KELLER, R., DAVIDSON, L.A. and SHOOK, D.R. (2003). How we are shaped: The biomechanics of gastrulation. Differentiation 71: 171-205.
13. KOEHL, M.A.R. (1990). Biomechanical approaches to morphogenesis. Sem. Dev. Biol. 1: 367-378.
14. KOMINAMI, T and TAKATA, H. (2004). Gastrulation in the sea urchin embryo: A model system for analyzing the morphogenesis of a monolayered epithelium. Develop. Growth Differ. 46: 309-326.
15. LANE, M.C., KOEHL, M.A.R., WILT, F. and KELLER, R. (1993). A role for regulated secretion of apical extracellular matrix during epithelial invagination in the sea urchin. Development 117: 1049-1060.
16. MAJHENC, J., BOZIC, B., SVETINA, S. and ZEKS, B. (2004). Phospholipid membrane bending as assessed by the shape sequence of giant oblate phospholipid vesicles. Biochim. Biophys. Acta 1664: 257-266.
17. MIAO, L., SEIFERT, U., WORTIS, M. and DOEBEREINER, H.G. (1994). Budding transitions of fluid-bilayer vesicles: the effect of the area difference elasticity. Phys. Rev. E 49: 5389-5407.
18. NEWMAN, S. A. and COMPER, W. D. (1990). Generic physical mechanisms of morphogenesis and pattern formation. Development 110: 1-18.
19. ODELL, G.M., OSTER, G., ALBERCH, P. and BURNSIDE, B. (1980). The mechanical basis of morphogenesis. I. Epithelial folding and invagination. Dev. Biol. 85: 446-462.
20. OU-YANG, Z-C. and HELFRICH, W. (1989). Bending energy of vesicle membranes: General expressions for the first, second and third variation of the shape energy and applications to spheres and cylinders. Phys. Rev. A 39: 5280-5288.
21. SEIFERT, U. BERNDL, K. and LIPOWSKY, R. (1991). Shape transformations of vesicle-phase-diagram for spontaneous-curvature and bilayer-coupling models. Phys. Rev. A 44: 1182-1202.
22. SHEETZ, M.P. and SINGER, S.J. (1974). Biological membranes as bilayer couples. A molecular mechanism of drug-erythrocyte interaction. Proc. Natl. Acad. Sci. USA 71: 4457-4461.
23. SPIEGEL, E., HOWARD, L. and SPIEGEL, M. (1989). Extracellular matrix of sea urchin and other marine invertebrate embryos. J. Morph. 199: 71-92.
24. SVETINA, S. and ZEKS, B. (1989). Membrane bending energy and shape determination of phospholipid vesicles and red blood cells. Eur. Biophys. J. 17: 101-111.
25. SVETINA, S. and ZEKS, B. (1991). Mechanical behavior of closed lamellar membranes as a possible common mechanism for the establishment of developmental shapes. Int. J. Dev. Biol. 35: 359-365.
26. SVETINA, S. and ZEKS, B. (1992). The elastic deformability of closed multilayered membranes is the same as that of a bilayer membrane. Eur. Biophys. J. 21: 251-255.
27. SVETINA, S. and ZEKS, B. (1996). Elastic properties of closed bilayer membranes and the shapes of giant phospholipid vesicles. In: (Lasic, D.D. and Barenholz, Y. Eds.). Handbook of Nonmedical Applications of Liposomes. CRC Press, Boca Raton. Vol. I: 13-42.
28. SVETINA, S. and ZEKS, B. (2002). Shape behavior of lipid vesicles as the basis of some cellular processes. Anat. Rec. 268: 215-225.
29. TAKATA, H. and KOMINAMI, T. (2001). Shrinkage and expansion of blastocoel affect the degree of invagination in sea urchin embryos. Zool. Sci. 18: 1097-1105.
30. VERHAS, J. (1997). Continuous shape transformations of liquid crystal membrane vesicles. J. Mol. Liquids 72: 337-346.
31. WAUGH, R.E., SONG J., SVETINA, S. and ZEKS, B. (1992). Local and non-local curvature elasticity in bilayer membranes by tether formation from lecithin vesicles. Biophys. J. 61: 974-982.