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Effects of the ecdysoneless mutant on synaptic efficacy and structure at the neuromuscular junction in Drosophila larvae during normal and prolonged development

Producción científica: Articlerevisión exhaustiva

23 Citas (Scopus)

Resumen

Hormonal regulation in development and maintenance of synaptic transmission involves examination of both the presynaptic and postsynaptic components and a system in which the hormones can be controlled. We used the ecdysoneless heat-sensitive mutation (l(3)ecd1/l(3)ecd1) of Drosophila to provide the ability to regulate endogenous ecdysone production at various larval stages. In conjunction, we used the neuromuscular junctions of Drosophila since they offer the advantage of assessable preparations for both morphological and physiological measures. The growth in the Ib and Is motor nerve terminals and the corresponding muscle 6 in segment 4 of the larval Drosophila throughout the third instar stage in the presence of normal and a much reduced endogenous ecdysone level was investigated. Muscle 6 and the motor nerve terminals parallel in growth throughout the third instar. The nerve terminals increase in length and varicosity number, thus providing an increase in the number of synaptic release sites. The ecdysoneless larvae also show an increase in muscle size, however the Is and Ib motor nerve terminals do not mature to the extent of the wild-type ecdysone producing flies. The motor nerve terminal length is shorter with fewer numbers of varicosities per terminal. In spite of a shorter nerve terminal and fewer varicosities, with an increasing muscle fiber, the compound excitatory junctional potentials of Ib and Is in the ecdysoneless flies are larger, which is suggestive of synaptic structural modification. This study demonstrates ecdysone's role in modifying nerve terminal development and neuromuscular junction function.

Idioma originalEnglish
Páginas (desde-hasta)193-200
Número de páginas8
PublicaciónNeuroscience
Volumen106
N.º1
DOI
EstadoPublished - sept 3 2001

Nota bibliográfica

Funding Information:
Funding was provided by NSF Grants IBN-9808631 (R.L.C.) and NSF-ILI-DUE 9850907 (R.L.C.). We thank Dr. Vincent C. Henrich, University of North Carolina at Charlotte for supplying the ecd 1 flies. We also thank Drs. Doug Harrison and Grace Jones and their laboratory members (University of Kentucky) for helping to maintain the stocks and trouble shooting with maintenance of flies.

Financiación

Funding was provided by NSF Grants IBN-9808631 (R.L.C.) and NSF-ILI-DUE 9850907 (R.L.C.). We thank Dr. Vincent C. Henrich, University of North Carolina at Charlotte for supplying the ecd 1 flies. We also thank Drs. Doug Harrison and Grace Jones and their laboratory members (University of Kentucky) for helping to maintain the stocks and trouble shooting with maintenance of flies.

FinanciadoresNúmero del financiador
NSF-ILI-DUE9850907
National Science Foundation (NSF)IBN-9808631

    ASJC Scopus subject areas

    • General Neuroscience

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