Ecdysone and the cell cycle: Investigations in a mosquito cell line

Journal of Insect Physiology

Volumn 56, Issue 10, 2010, Pages 1396-1401

  Fallon, Ann M ^a   Gerenday, Anna ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

20 Hydroxyecdysone; Cell cycle; Insect cell lines; Mosquito

Indexed keywords

ECDYSTERONE; INSECT HORMONE;

CYTOLOGY; ESTROGENIC COMPOUND; GENE EXPRESSION; HORMONE; MOSQUITO; PHYSIOLOGICAL RESPONSE; PROTEIN; STEROID;

AEDES; ANIMAL; ARTICLE; CELL CYCLE; CELL LINE; CYTOLOGY; GENE EXPRESSION REGULATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; MAMMAL; METABOLISM;

AEDES; ANIMALS; CELL CYCLE; CELL LINE; ECDYSTERONE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; INSECT HORMONES; MAMMALS;

AEDES ALBOPICTUS; DROSOPHILA MELANOGASTER; HEXAPODA; LEPIDOPTERA; MAMMALIA; PLODIA INTERPUNCTELLA; VERTEBRATA;

EID: 77955419434     PISSN: 00221910     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jinsphys.2010.03.016     Document Type: Article

References (51)

1. Butenandt A., Karlson P. Uber die Isolierung eines metamorphose-hormone der Insekten in kristallisierter form. Zeitschrift fur Naturforschung 1954, 9b:389-391.
2. Cherbas L., Yonge C.D., Cherbas P., Williams C.M. The morphological response of Kc-H cells to ecdysteroids: Hormonal specificity. W. Roux's Archives of Developmental Biology 1980, 189:1-15.
3. Dobens L., Rudolph K., Berger E.M. Ecdysterone regulatory elements function as both transcriptional activators and repressors. Molecular and Cellular Biology 1991, 11:1846-98147.
4. Eccleston E.D., Gerenday A., Fallon A.M. Leveraging genomic databases: from an Aedes albopictus cell line to the malaria vector Anopheles gambiae via the Drosophila genome project. Insect Molecular Biology 2002, 11:187-195.
5. Echalier G. Drosophila Cells in Culture 1997, Academic Press, New York, 702 pp.
6. Fallon A.M. Transfection of cultured mosquito cells. Molecular Biology Of Insect Disease Vectors 1997, 430-443. Chapman and Hall, New York. J.M. Crampton, C.B. Beard, C. Louis (Eds.).
7. Fallon A.M., Kurtti T.J. Cultured cells as a tool for analysis of gene expression. Biology of Disease Vectors 2005, 539-549. Elsevier, New York. 2nd ed. W.C. Marquardt (Ed.).
8. Fallon A.M., Sun D. Exploration of mosquito immunity using cells in culture. Insect Biochemistry and Molecular Biology 2001, 31:263-278.
9. Fox E.M., Andrade J., Shupnik M.A. Novel actions of estrogen to promote proliferation: Integration of cytoplasmic and nuclear pathways. Steroids 2009, 74:622-627.
10. Fraenkel G. Hormone causing pupation in the blowfly Calliphora erythrocephala. Proceedings of the Royal Society of London, Series B 1935, 118:1.
11. Galesi A.L.L., Pereira C.A., Moraes A.M. Culture of transgenic Drosophila melanogaster Schneider 2 cells in serum-free media based on TC100 basal medium. Biotechnology Journal 2007, 2:1399-1407.
12. Gerenday A., Fallon A.M. Cell cycle parameters in Aedes albopictus mosquito cells. In vitro Cellular and Developmental Biology-Animal 1996, 32:307-312.
13. Gerenday A., Fallon A.M. Ecdysone-induced accumulation of mosquito cells in the G1 phase of the cell cycle. Journal of Insect Physiology 2004, 50:831-838.
14. Gerenday A., Blauwkamp T.S., Fallon A.M. Synchronization of Aedes albopictus mosquito cells using hydroxyurea. Insect Molecular Biology 1997, 6:191-196.
15. Gillies S., Stollar V. Conditions necessary for inhibition of protein synthesis and production of cytopathic effect in Aedes albopictus cells infected with vesicular stomatitis virus. Molecular and Cellular Biology 1982, 2:66-75.
16. Goldschmidt R.B. Some experiments on spermatogenesis in vitro. Proceedings of the National Academy of Science USA 1915, 1:220-222.
17. Goto S., Loeb M.J., Takeda M. Bombyxin stimulates proliferation of cultured stem cells derived from Heliothis virescens and Mamestra brassicae larvae. In vitro Cellular and Developmental Biology-Animal 2005, 40:38-42.
18. Grace T.D.C. Establishment of four strains of cells from insect tissues grown in vitro. Nature 1962, 195. 788-789, 1962.
19. Hatt P.J., Moriniere M., Oberlander H., Porcheron P. Roles for insulin and ecdysteroids in differentiation of an insect cell line of epidermal origin. In Vitro Cellular and Developmental Biology 1994, 30A:717-720.
20. Hayflick L. The limited in vitro lifetime of human diploid cell strains. Experimental Cell Research 1965, 37:614-636.
21. Jayachandran G., Fallon A.M. Evidence for expression of EcR and USP components of the 20-hydroxyecdysone receptor by a mosquito cell line. Archives of Insect Biochemistry and Physiology 2000, 43:87-96.
22. Jayachandran G., Fallon A.M. Antisense expression of the 20-hydroxyecdysone receptor (EcR) in transfected mosquito cells uncovers a new EcR isoform that varies at the C-terminal end. In vitro Cellular and Developmental Biology-Animal 2001, 37-522-529.
23. Jayachandran G., Fallon A.M. Decreased survival of mosquito cells after stable transfection with a Drosophila ecdysteroid response element: possible involvement of a 40kDa DNA binding protein. Journal of Insect Science 2002, 2(21). Insectscience.org/2.21.
24. Johnston A.M., Fallon A.M. Characterization of the ribosomal proteins from mosquito (Aedes albopictus) cells. European Journal of Biochemistry 1985, 150:507-515.
25. Kopec S. Studies on the necessity of the brain for the inception of insect metamorphosis. Biological Bulletin 1922, 42:323-342.
26. Lan Q., Gerenday A., Fallon A.M. Cultured Aedes albopictus cells synthesize hormone-inducible proteins. In vitro Cellular and Developmental Biology-Animal 1993, 29:813-818.
27. Lin T., Ambasudhan R., Yuan Z., Li W., Hilcove S., Abujarour R., Lin X., Hahm H.S., Hao E., Hayek A., Ding S. A chemical platform for improved induction of human iPSCs. Nature Methods 2009, 6:805-808.
28. Liu C.-C., Wu S.-C. Mosquito and mammalian cells grown on microcarriers for four-serotype dengue virus production: variations in virus titer, plaque morphology, and replication rate. Biotechnology and Bioengineering 2004, 85:482-488.
29. Loeb M.J., Martin P.A.W., Hakim R.S., Goto S., Takeda M. Regeneration of cultured midgut cells after exposure to sublethal doses of toxin from two strains of Bacillus thuringiensis. Journal of Insect Physiology 2001, 47:599-606.
30. Lynn D.E. Novel techniques to establish new insect cell lines. In vitro Cellular and Developmental Biology-Animal 2001, 37:319-321.
31. Micchelli C.A., Perrimon N. Evidence that stem cells reside in the adult Drosophila midgut epithelium. Nature 2006, 439:475-479.
32. Mitsuhashi J., Maramorosch K. Leafhopper tissue culture: embryonic, nymphal and imaginal tissues from aseptic insects. Contributions of the Boyce Thompson Institute 1964, 22:435-460.
33. Miura K., Wang S.F., Raikhel A.S. Two distinct subpopulations of the ecdysone receptor complex in the female mosquito during vitellogenesis. Molecular and Cellular Endocrinology 1999, 156:111-120.
34. Monroe T.J., Muhlmann-Diaz M.C., Kovach M.J., Carlson J.O., Bedford J.S., Beaty B.J. Stable transformation of a mosquito cell line results in extraordinarily high copy numbers of the plasmid. Proceedings of the National Academy of Sciences USA 1992, 89:5725-5729.
35. Mottier V., Siaussat D., Bozzolan F., Auzoux-Bordenave S., Porcheron P., Debernard S. The 20-hydroxyecdysone-induced cellular arrest in G2 phase is preceded by an inhibition of cyclin expression. Insect Biochemistry and Molecular Biology 2004, 34:51-60.
36. Mukherjee A.B., Herrera R.J. Replication pattern of double minutes derived from an insect cell line. Experientia 1985, 41:85-86.
37. Nakagawa Y., Henrich V.C. Arthropod nuclear receptors and their role in molting. FEBS Journal 2009, 276:6128-6157.
38. Saarinen M.A., Murhammer D.W. Culture in the rotating-wall vessel affects recombinant protein production capability of two insect cell lines in different manners. In vitro Cellular and Developmental Biology-Animal 2000, 36:362-366.
39. Safe S., Kim K. Non-classical genomic estrogen receptor (ER)/specificity protein and ER/activating protein-1 signaling pathways. Journal of Molecular Endocrinology 2008, 41:263-275.
40. Sanchez A.M., Simoncini T. Extra-nuclear signaling of the ERa to the actin cytoskeleton in the central nervous system. Steroids 2009, 10.1016/j.steroids.2009.12.003.
41. Sarver N., Stollar V. Sindbis virus-induced cytopathic effect in clones of Aedes albopictus (Singh) cells. Virology 1977, 80:390-400.
42. Shih K.M., Gerenday A., Fallon A.M. Culture of mosquito cells in Eagle's medium. In vitro Cellular and Developmental Biology-Animal 1998, 34:629-630.
43. Shotkoski F.A., Fallon A.M. Genetic changes in methotrexate-resistant mosquito cells. Archives of insect Biochemistry and Physiology 1990, 15:79-92.
44. Siaussat D., Bozzolan F., Porcheron P., Debernard S. Identification of steroid hormone signaling pathway in insect cell differentiation. Cellular and Molecular Life Sciences 2007, 64:365-376.
45. Siaussat D., Bozzolan F., Porcheron P., Debernard S. The 20-hydroxyecdysone-induced signaling pathway in G2/M arrest of Plodia interpunctella imaginal wing cells. Insect Biochemistry and Molecular Biology 2008, 38:529-539.
46. Singh K.R.P. Cell cultures derived from larvae of Aedes albopictus (Skuse) and Aedes aegypti (L). Current Science 1967, 36:506-508.
47. Swanhart L., Kupsco J., Duronio R.J. Developmental control of growth and cell cycle progression in Drosophila. Methods in Molecular Biology, Vol. 296: Cell cycle control: Mechanisms and Protocols 2005, 69-94. Humana Press, Totowa, New Jersey. T. Humphrey, G. Brooks (Eds.).
48. Wang S.F., Miura K., Miksicek R.J., Segraves W.A., Raikhel A.S. DNA binding and transactivation characteristics of the mosquito ecdysone receptor-ultraspiracle complex. Journal of Biological Chemistry 1998, 273:27531-27540.
49. Wright W.E., Shay J.W. Telomere dynamics in cancer progression and prevention: fundamental differences in human and mouse telomere biology. Nature Medicine 2000, 6:849-851.
50. Wyatt S.S. Culture in vitro of tissue from the silkworm Bombyx mori L. Journal of General Physiology 1956, 39:841-852.
51. Yao T.P., Froman B.M., Jiang Z., Cherbas L., Chen J.D., McKeown M., Cherbas P., Evans R.M. Functional ecdysone receptor is the product of EcR and Ultraspiracle genes. Nature 1993, 366:476-479.