Ultrastructure and morphology of midgut visceral muscle in early pupal Aedes aegypti mosquitoes

Tissue and Cell

Volumn 40, Issue 2, 2008, Pages 127-141

  Bernick, E P ^a   Moffett, S B ^a   Moffett, D F ^a  

^a WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

Aedes aegypti; Development; Midgut; Pupae; Ultrastructure; Visceral muscle

Indexed keywords

AEDES AEGYPTI; ARTICLE; CELL MEMBRANE; CONTROLLED STUDY; DEGRADATION; FEMALE; INSECT DEVELOPMENT; LARVA; MALE; METAMORPHOSIS; MIDGUT; MORPHOLOGY; MUSCLE CELL; NEUROMUSCULAR SYNAPSE; NONHUMAN; SCANNING ELECTRON MICROSCOPY; SEX DIFFERENCE; TRANSMISSION ELECTRON MICROSCOPY; ULTRASTRUCTURE;

AEDES AEGYPTI;

EID: 39749143490     PISSN: 00408166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tice.2007.11.001     Document Type: Article

References (22)

1. Beaulaton J., and Lockshin R.A. Ultrastructural study of the normal degeneration of the intersegmental muscles of Antherea polyphemus and Manduca sexta (Insecta, Lepidoptera) with particular reference to cellular autophagy. J. Morphol. 154 (1976) 39
2. Bernick E.P., Moffett S.B., and Moffett D.F. Organization, ultrastructure, and development of midgut visceral muscle in larval Aedes aegypti. Tissue Cell 39 (2007) 277-292
3. Christophers S.R. Aedes aegypti, The Yellow Fever Mosquito: Its Life History, Binomics, and Structure (1960), Cambridge University Press, London, England
4. Clark T.M., Hutchinson M.J., Heugel K.L., Moffett S.B., and Moffett D.F. Additional morphological and physiological heterogeneity within the midgut of larval Aedes aegypti revealed by histology, electrophysiology, and effects of Bacillus thuringiensis endotoxin. Tissue Cell 37 (2005) 457-468
5. Clements A.N. The Biology of Mosquitoes, vol. 1: Development, Nutrition, and Reproduction (1992), Chapman and Hall, New York
6. Copenhaver P.F., Horgan A.M., and Combes S. An identified set of visceral muscle bands is essential for the guidance of migratory neurons in the enteric nervous system of Manduca sexta. Dev. Biol. 179 (1996) 412-426
7. Goldstein M.A., and Burdette W.J. Striated visceral muscle of Drosophila melanogaster. J. Morphol. 134 (1971) 315-334
8. Haas A.L., Baboshina O., Williams B., and Schwartz L.M. Coordinated induction of the ubiquitin conjugation pathway accompanies the developmentally programed death of insect skeletal muscle. J. Biol. Chem. 270 (1995) 9407-9412
9. Hegstrom C.D., and Truman J.W. Synapse loss and axon retraction in response to local muscle degeneration. J. Neurobiol. 31 (1996) 175-188
10. Hegstrom C.D., Riddiford L.M., and Truman J.W. Steroid and neuronal regulation of ecdysone receptor expression during metamorphosis of muscle in the moth, Manduca sexta. J. Neurosci. 18 (1998) 1786-1794
11. Holzl H., Kapelari B., Kellerman J., Seemüller E., Sümegi M., Udvari A., Medalia O., Sperling J., Müller S., Engel A., and Baumeister W. The regulatory complex of Drosophila melanogaster 26S proteasomes: subunit composition and localization of a deubiquitylating enzyme. J. Cell Biol. 150 (2000) 119-129
12. Klapper R. The longitudinal visceral musculature of Drosophila melanogaster persists through metamorphosis. Mech. Dev. 95 (2000) 47-54
13. Löw P., Hastings R.A., Dawson S.P., Sass M., Billett M.A., Mayer R.J., and Reynolds S.E. Localization of 26S proteasomes with different subunit composition in insect muscles undergoing programmed cell death. Cell Death Differ. 7 (2000) 1210-1217
14. Margam V., Gelman D.B., and Palli S.R. Ecdysteroid titers and developmental expression of ecdysteroid-regulated genes during metamorphosis of the yellow fever mosquito, Aedes aegypti (Diptera: Culicidae). J. Insect Physiol. 52 (2006) 558-568
15. Moffett S.B., and Moffett D.F. Comparison of immunoreactivity to serotonin, FMRF-amide and SCPb in the gut and visceral nervous system of larvae, pupae, and adults of the yellow fever mosquito Aedes aegypti. J. Insect Sci. 5 (2005) 20
16. Mykles D.L. Biochemical properties of insect and crustacean proteasomes. Mol. Biol. Rep. 24 (1997) 133-138
17. O'Brien J.F. Development of the muscular network of the midgut in the larval stages of the mosquito Aedes aegypti. J. N.Y. Entomol. Soc. 73 4 (1965) 226-231
18. Park S.S., and Shahabuddin M. Structural organization of posterior midgut muscles in mosquitoes, Aedes aegypti and Anopheles gambiae. J. Struct. Biol. 129 (2000) 30-37
19. Rockel B., Peters J., Kühlmorgen B., Glaeser R.M., and Baumeister W. A giant protease with a twist: the TPP complex from drosophila studied by electron microscopy. EMBO J. 21 (2002) 5979-5984
20. Schwartz L.M. Insect muscle as a model for programmed cell death. J. Neurobiol. 23 (1992) 1312-1326
21. Sharon M., Witt S., Felderer K., Rockel B., Baumeister W., and Robinson C.V. 20S proteasomes have the potential to keep substrates in store for continual degradation. J. Biol. Chem. 281 14 (2006) 9569-9575
22. Truman J.W., and Reiss S.E. Neuromuscular metamorphosis in the moth Manduca sexta: hormonal regulation of synapse loss and remodeling. J. Neurosci. 15 (1995) 4815-4826