Epithelial reorganization events during late extraembryonic development in a hemimetabolous insect

Developmental Biology

Volumn 340, Issue 1, 2010, Pages 100-115

  Panfilio, Kristen A ^a   Roth, Siegfried ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

Author keywords

Amnion; Apoptosis; Dorsal closure; Epithelial morphogenesis; Filamentous actin (F actin); Insect extraembryonic membranes; Katatrepsis; Oncopeltus fasciatus; Serosa; Supracellular purse string

Indexed keywords

AMNION; ANIMAL CELL; APOPTOSIS; ARTICLE; CELL SHAPE; CONTROLLED STUDY; DROSOPHILA MELANOGASTER; EMBRYO; EMBRYO DEVELOPMENT; EPITHELIUM; IMAGE PROCESSING; INSECT; INSECT DEVELOPMENT; MORPHOGENESIS; NONHUMAN; ONCOPELTUS FASCIATUS; PRIORITY JOURNAL; RNA INTERFERENCE;

DROSOPHILA MELANOGASTER; HEXAPODA; ONCOPELTUS FASCIATUS;

EID: 77649187605     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2009.12.034     Document Type: Article

References (78)

1. Anderson D.T. The development of hemimetabolous insects. In: Counce S.J., and Waddington C.H. (Eds). Developmental Systems: Insects Vol. 1 (1972), Academic Press, London 95-163
2. Ando H. Everted embryos of dragonflies produced by ligation. Sci. Rep. Tokyo Kyoiku Daig. Sect. B 8 (1955) 65-74
3. Bedford G.O. The development of the egg of Didymuria violescens (Phasmatodea: Phasmatidae: Podacanthinae)-embryology and determination of the stage at which first diapause occurs. Aust. J. Zool. 18 (1970) 155-169
4. Berger-Twelbeck P., Hofmeister P., Emmling S., and Dorn A. Ovicide-induced serosa degeneration and its impact on embryonic development in Manduca sexta (Insecta: Lepidoptera). Tissue Cell 35 (2003) 101-112
5. Bullière F. Établissement des stades du développement embryonnaire d'un insecte dictyoptère: Blabera craniifer Burm. Ann. Embryol. Morph. 2 (1969) 121-138
6. Burridge K. Are stress fibres contractile?. Nature 294 (1981) 691-692
7. Butt F.H. Embryology of the Milkweed Bug, Oncopeltus fasciatus (Hemiptera) (1949), Agriculture Experiment Station, Cornell University
8. Byars C.L., Bates K.L., and Letsou A. The dorsal-open group gene raw is required for restricted DJNK signaling during closure. Development 126 (1999) 4913-4923
9. Chen G., Handel K., and Roth S. The maternal NF-kappaB/Dorsal gradient of Tribolium castaneum: dynamics of early dorsoventral patterning in a short-germ beetle. Development 127 (2000) 5145-5156
10. Cobben R.H. Evolutionary Trends in the Heteroptera, Part I. Eggs, Architecture of the Shell, Gross Embryology and Eclosion (1968), Centre for Agricultural Publishing and Documentation, Wageningen
11. Deguchi S., and Sato M. Biomechanical properties of actin stress fibers of non-motile cells. Biorheology 46 (2009) 93-105
12. Dorn A. Ultrastructure of embryonic envelopes and integument of Oncopeltus fasciatus Dallas (Insecta, Heteroptera) I. Chorion, amnion, serosa, integument. Zoomorphologie 85 (1976) 111-131
13. Dorn A. Ultrastructure of embryonic envelopes and integument of Oncopeltus fasciatus Dallas (Insecta, Heteroptera) II. Secondary dorsal organ. Zoomorphologie 89 (1978) 57-72
14. Enslee E.C., and Riddiford L.M. Blastokinesis in embryos of the bug, Pyrrhocoris apterus. A light and electron microscopic study 1. Normal blastokinesis. J. Embryol. Exp. Morph. 61 (1981) 35-49
15. Fernández B.G., Arias A.M., and Jacinto A. Dpp signalling orchestrates dorsal closure by regulating cell shape changes both in the amnioserosa and in the epidermis. Mech. Dev. 124 (2007) 884-897
16. Frank L.H., and Rushlow C. A group of genes required for maintenance of the amnioserosa tissue in Drosophila. Development 122 (1996) 1343-1352
17. Gorfinkiel N., Blanchard G.B., Adams R.J., and Arias A.M. Mechanical control of global cell behaviour during dorsal closure in Drosophila. Development 136 (2009) 1889-1898
18. Gorman M.J., Kankanala P., and Kanost M.R. Bacterial challenge stimulates innate immune responses in extra-embryonic tissues of tobacco hornworm eggs. Insect Mol. Biol. 13 (2004) 19-24
19. Hagan H.R. Observations on the embryonic development of the mantid Paratenodera sinensis. J. Morph. 30 (1917) 223-243
20. Handel K., Grünfelder C.G., Roth S., and Sander K. Tribolium embryogenesis: a SEM study of cell shapes and movements from blastoderm to serosal closure. Dev. Genes Evol. 210 (2000) 167-179
21. Harden N. Signaling pathways directing the movement and fusion of epithelial sheets: lessons from dorsal closure in Drosophila. Differentiation 70 (2002) 181-203
22. Heitzler P., Haenlin M., Ramain P., Calleja M., and Simpson P. A genetic analysis of pannier, a gene necessary for viability of dorsal tissues and bristle positioning in Drosophila. Genetics 143 (1996) 1271-1286
23. Heming B.S., and Huebner E. Development of the germ cells and reproductive primordia in the male and female embryo of Rhodnius prolixus Stål (Hemiptera: Reduviidae). Can. J. Zool. 72 (1994) 1100-1119
24. Hutson M.S., Tokutake Y., Chang M.-S., Bloor J.W., Venakides S., Kiehart D.P., and Edwards G.S. Forces for morphogenesis investigated with laser microsurgery and quantitative modeling. Science 300 (2003) 145-149
25. Jacinto A., and Martin P. Morphogenesis: unravelling the cell biology of hole closure. Curr. Biol. 11 (2001) R705-R707
26. Jacinto A., Wood W., Balayo T., Turmaine M., Martinez-Arias A., and Martin P. Dynamic actin-based epithelial adhesion and cell matching during Drosophila dorsal closure. Curr. Biol. 10 (2000) 1420-1426
27. Jacinto A., Wood W., Woolner S., Hiley C., Turner L., Wilson C., Martinez-Arias A., and Martin P. Dynamic analysis of actin cable function during Drosophila dorsal closure. Curr. Biol. 12 (2002) 1245-1250
28. Jacinto A., Woolner S., and Martin P. Dynamic analysis of dorsal closure in Drosophila: from genetics to cell biology. Dev. Cell 3 (2002) 9-19
29. Jura C. Development of apterygote insects. In: Counce S.J., and Waddington C.H. (Eds). Developmental Systems: Insects Vol. 1 (1972), Academic Press, London 49-94
30. Kelly G.M., and Huebner E. Embryonic development of the hemipteran insect Rhodnius prolixus. J. Morph. 199 (1989) 175-196
31. Kershaw J.C. Development of an embiid. J. R. Micr. Soc. 34 (1914) 24-27
32. Kiehart D.P., Galbraith C.G., Edwards K.A., Rickolla W.L., and Montague R.A. Multiple forces contribute to cell sheet morphogenesis for dorsal closure in Drosophila. J. Cell Biol. 149 (2000) 471-490
33. Knower H.M. The embryology of a termite, Eutermes (Rippertii?). J. Morph. 16 (1900) 505-568
34. Lamka M.L., and Lipshitz H.D. Role of the amnioserosa in germ band retraction of the Drosophila melanogaster embryo. Dev. Biol. 214 (1999) 102-112
35. Laplante C., and Nilson L.A. Differential expression of the adhesion molecule Echinoid drives epithelial morphogenesis in Drosophila. Development 133 (2006) 3255-3264
36. Lynch J.A., Panfilio K.A., and Nunes da Fonseca R. As Tribolium matures as a model insect, coleopteran community congregates in Cologne. Dev. Genes Evol. 219 (2010) 531-533
37. Mahr E. Normale Entwicklung, Pseudofurchung und die Bedeutung des Furchungszentrums im Ei des Heimchens (Gryllus domesticus). Z. Morph. Ökol. Tiere 49 (1960) 263-311
38. Martin A.C., Kaschube M., and Wieschaus E.F. Pulsed contractions of an actin-myosin network drive apical constriction. Nature 457 (2009) 495-499
39. Martin P., and Lewis J. Actin cables and epidermal movement in embryonic wound healing. Nature 360 (1992) 179-183
40. Masumoto M., and Machida R. Development of embryonic membranes in the silverfish Lepisma saccharina Linnaeus (Insecta: Zygentoma, Lepismatidae). Tissue Cell 38 (2006) 159-169
41. Mellanby H. The later embryology of Rhodnius prolixus. Q. J. Microsc. Sci. 79 (1936) 1-42
42. Miller A. Embryonic membranes, yolk cells, and morphogenesis of the stonefly Pteronarcys proteus Newman. Ann. Entomol. Soc. Amer. 33 (1940) 347-477
43. Mori H. The distribution of the columnar serosa of eggs among the families of Heteroptera, in relation to phylogeny and systematics. Jap. J. Zool. 16 (1970) 89-98
44. Mori H. Water absorption by the columnar serosa in the eggs of the waterstrider, Gerris paludum insularis. J. Insect Physiol. 18 (1972) 675-681
45. Mori H. Everted embryos obtained after cauterization of eggs of the waterstrider, Gerris paludum insularis Motschulsky. Annot. Zool. Japon 48 (1975) 252-261
46. Panfilio K.A. Extraembryonic development in insects and the acrobatics of blastokinesis. Dev. Biol. 313 (2008) 471-491
47. RNAi-induced failure in the milkweed bug Oncopeltus fasciatus. Dev. Biol. 333 (2009) 297-311
48. Panfilio K.A., Liu P.Z., Akam M., and Kaufman T.C. Oncopeltus fasciatus zen is essential for serosal tissue function in katatrepsis. Dev. Biol. 292 (2006) 226-243
49. Pellegrin S., and Mellor H. Actin stress fibers. J. Cell Sci. 120 (2007) 3491-3499
50. Peralta X.G., Toyama Y., Hutson M.S., Montague R., Venakides S., Kiehart D.P., and Edwards G.S. Upregulation of forces and morphogenic asymmetries in dorsal closure during Drosophila development. Biophys. J. 92 (2007) 2583-2596
51. Rafiqi A.M., Lemke S., Ferguson S., Stauber M., and Schmidt-Ott U. Evolutionary origin of the amnioserosa in cyclorrhaphan flies correlates with spatial and temporal expression changes of zen. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 234-239
52. Rakshpal R. Morphogenesis and embryonic membranes of Gryllus assimilis (Fabricius) (Orthoptera: Gryllidae). Proc. R. Ent. Soc. Lond. (A) 37 (1962) 1-12
53. Raminani L.N., and Cupp E.W. Early embryology of Aedes aegypti (L.) (Diptera: Culicidae). Int. J. Insect Morphol. Embryol. 4 (1975) 517-528
54. Raminani L.N., and Cupp E.W. Embryology of Aedes aegypti (L.) (Diptera: Culicidae): Organogenesis. Int. J. Insect Morphol. Embryol. 7 (1978) 273-296
55. Reed B.H., Wilk R., and Lipshitz H.D. Downregulation of Jun kinase signaling in the amnioserosa is essential for dorsal closure of the Drosophila embryo. Curr. Biol. 11 (2001) 1098-1108
56. Reed B.H., Wilk R., Schöck F., and Lipshitz H.D. Integrin-dependent apposition of Drosophila extraembryonic membranes promotes morphogenesis and prevents anoikis. Curr. Biol. 14 (2004) 372-380
57. Rezende G.L., Martins A.J., Gentile C., Farnesi L.C., Pelajo-Machado M., Peixoto A.A., and Valle D. Embryonic desiccation resistance in Aedes aegypti: presumptive role of the chitinized serosal cuticle. BMC Dev. Biol. 8 (2008) 82
58. Roonwal M.L. Studies on the embryology of the African migratory locust, Locusta migratoria migratorioides R. and F. I. The early development, with a new theory of multi-phased gastrulation among insects. Phil. Trans. R. Soc. Lond. B 226 (1936) 391-421
59. Roth S., and Hartenstein V. Development of Tribolium castaneum. Dev. Genes Evol. 218 (2008) 115-118
60. Rugendorff A., Younossi-Hartenstein A., and Hartenstein V. Embryonic origin and differentiation of the Drosophila heart. Roux's Arch. Dev. Biol. 203 (1994) 266-280
61. Sander K. Analyse des ooplasmatischen Reaktionssytems von Euscelis plebejus Fall. (Cicadina) durch Isolieren und Kombinieren von Keimteilen I. Die Differenzierungsleistungen vorderer und hinterer Eiteile. Roux' Arch. Entwickmech. 151 (1959) 430-497
62. Sander K. Analyse des ooplasmatischen Reaktionssystems von Euscelis plebejus Fall (Cicadina) durch Isolieren und Kombinieren von Keimteilen II. Die Differenzierungsleistungen nach Verlangern von Hinterpolmaterial. Roux' Arch. Entwickmech. 151 (1960) 660-707
63. Sander K. Morphogenetic movements in insect embryogenesis. In: Lawrence P.A. (Ed). Insect Development Vol. 8 (1976), Blackwell Scientific Publications, Oxford 35-52
64. Schmidt-Ott U. The amnioserosa is an apomorphic character of cyclorrhaphan flies. Dev. Genes Evol. 210 (2000) 373-376
65. Slifer E.H. Insect development. III. Blastokinesis in the living grasshopper egg. Biol. Zbl. 52 (1932) 223-229
66. Solon J., Kaya-Çopur A., Colombelli J., and Brunner D. Pulsed forces timed by a ratchet-like mechanism drive directed tissue movement during dorsal closure. Cell 137 (2009) 1331-1342
67. Stronach B.E., and Perrimon N. Investigation of leading edge formation at the interface of amnioserosa and dorsal ectoderm in the Drosophila embryo. Development 128 (2001) 2905-2913
68. Technau G.M. A single cell approach to problems of cell lineage and commitment during embryogenesis of Drosophila melanogaster. Development 100 (1987) 1-12
69. Toyama Y., Peralta X.G., Wells A.R., Kiehart D.P., and Edwards G.S. Apoptotic force and tissue dynamics during Drosophila embryogenesis. Science 321 (2008) 1683-1686
70. Tribolium Genome Sequencing Consortium. The genome of the model beetle and pest Tribolium castaneum. Nature 452 (2008) 949-955
71. Truckenbrodt W. Über die Entstehung der Serosa im besamten und im unbesamten Ei von Odontotermes badius Hav. (Insecta, Isoptera). Z. Morph. Tiere 76 (1973) 193-208
72. Truckenbrodt W. The embryonic covers during blastokinesis and dorsal closure of the normal and of the actinomycin D treated egg of Odontotermes badius (Hav.) (Insecta, Isoptera). Zool. Jb. Anat. Ont. 101 (1979) 7-18
73. Uchifune T., and Machida R. Embryonic development of Galloisiana yuasai Asahina, with special reference to external morphology (Insecta: Grylloblattodea). J. Morph. 266 (2005) 182-207
74. van der Zee M., Berns N., and Roth S. Distinct functions of the Tribolium zerknüllt genes in serosa specification and dorsal closure. Curr. Biol. 15 (2005) 624-636
75. Wada A., Kato K., Uwo M.F., Yonemura S., and Hayashi S. Specialized extraembryonic cells connect the embryonic and extraembryonic epidermis in response to Dpp during dorsal closure in Drosophila. Dev. Biol. 301 (2007) 340-349
76. Wheeler W.M. A contribution to insect embryology. J. Morph. 8 (1893) 1-160
77. Wood W., Jacinto A., Grose R., Woolner S., Gale J., Wilson C., and Martin P. Wound healing recapitulates morphogenesis in Drosophila embryos. Nat. Cell Biol. 4 (2002) 907-912
78. Woodland J.T. A contribution to our knowledge of lepismatid development. J. Morph. 101 (1957) 523-577