1996
DOI: 10.1002/(sici)1097-4695(199602)29:2<233::aid-neu8>3.0.co;2-b
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Postembryonic neurogenesis in the central nervous system of the tobacco hornworm,Manduca sexta. III. Spatial and temporal patterns of proliferation

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Cited by 13 publications
(6 citation statements)
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“…In grasshopper embryos, it appears that the selective pattern of cell death plays a prominent role in establishing the segmental differences in the neuronal types a lineage generates (Thompson and Siegler, 1993). A similar mechanism may also be involved during postembryonic neurogenesis in M. sexta (Booker et al, 1996). Thus, the large increases in BrdU-labeled cells in mushroom bodies of 20-hydroxyecdysone-treated D. punctata reported in the present study may be due to the prevention of cell death.…”
Section: Figuresupporting
confidence: 56%
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“…In grasshopper embryos, it appears that the selective pattern of cell death plays a prominent role in establishing the segmental differences in the neuronal types a lineage generates (Thompson and Siegler, 1993). A similar mechanism may also be involved during postembryonic neurogenesis in M. sexta (Booker et al, 1996). Thus, the large increases in BrdU-labeled cells in mushroom bodies of 20-hydroxyecdysone-treated D. punctata reported in the present study may be due to the prevention of cell death.…”
Section: Figuresupporting
confidence: 56%
“…We found that 20-hydroxyecdysone significantly increased the total number of BrdU-labeled cells during the long period of BrdU labeling, indicating that 20hydroxyecdysone not only enhances the mitotic rates of neurogenesis, but also increases the active life spans of mushroom bodies. In M. sexta, ecdysteroids appear to play a role in regulating the mitotic activity of anlage of adult optic lobes (Monsma and Booker, 1996). On the other hand, in the adult house cricket, A. domesticus, ecdysone appears to have an inhibitory effect on neurogenesis of mushroom bodies (Cayre et al, 1997).…”
Section: Figurementioning
confidence: 99%
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“…During metamorphosis many adult-specific neurons in the ventral ganglia are targeted by programmed cell death, particularly in abdominal segments (Bello et al, 2003;Booker and Truman, 1987;Booker et al, 1996). Furthermore, extensive cell death occurs during postembryonic development in the insect visual system, where cells are overproduced and those that do not make the appropriate targets are eliminated by apoptosis (Bonini and Fortini, 1999).…”
Section: Discussionmentioning
confidence: 99%
“…Doe and Technau 1993;Goodman and Doe 1993;Doe and Skeath 1996;Urban and Technau 1997;Campos-Ortega and Hartenstein 1997;Doe et al 1998;Skeath 1999;Matsuzaki 2000;Skeath and Thor 2003;Technau et al 2006). While most studies on insect neurogenesis have been carried out in grasshoppers and the fruit fly, studies on other insects such as the moth Manduca sexta (Booker and Truman 1987;Booker et al 1996) and the beetle Tenebrio molitor (Breidbach and Urbach 1996; indicate the universal presence of neuroblasts in this taxon (review . Neuroblasts were also studied in the silverfish, a primarily wingless insect and the array of neuroblasts in this species is evolutionarily conserved in the winged insects (Truman and Ball 1998).…”
Section: Introductionmentioning
confidence: 99%