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Respiratory metabolism of salivary glands during the late larval and prepupal development of Drosophila melanogaster

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    SYSNO ASEP0462352
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRespiratory metabolism of salivary glands during the late larval and prepupal development of Drosophila melanogaster
    Author(s) Farkaš, R. (SK)
    Sláma, Karel (BC-A) RID
    Number of authors2
    Source TitleJournal of Insect Physiology. - : Elsevier - ISSN 0022-1910
    Roč. 81, October 01 (2015), s. 109-117
    Number of pages9 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordssalivary glands ; in vitro culture ; metamorphosis
    Subject RIVED - Physiology
    Institutional supportBC-A - RVO:60077344
    UT WOS000361860300014
    EID SCOPUS84937204119
    DOI10.1016/j.jinsphys.2015.06.013
    AnnotationDuring the late larval period, the salivary glands (SG) of Drosophila show a cascade of cytological changes associated with exocytosis and the expectoration of the proteinaceous glue that is used to affix the pupariating larva to a substrate. After puparium formation (APF), SG undergo extensive cytoplasmic vacuolation due to endocytosis, vacuole consolidation and massive apocrine secretion. Here we investigated possible correlations between cytological changes, the puffing pattern in polytene chromosomes and respiratory metabolism of the SG. The carefully staged SG were explanted into small amounts (1 or 2 mu l) of tissue culture medium. The respiratory metabolism of single or up to 3 pairs of glands was evaluated by recording the rate of O-2 consumption using a scanning microrespirographic technique sensitive to sub-nanoliter volumes of the respiratory O-2 or CO2. The recordings were carried out at times between 8 h before pupariation (BPF), until 16 h APF, at which point the SG completely disintegrate. At the early wandering larval stage (8 h BPF), the glands consume 2 nl of O-2/gland/min (=2500 mu l O-2/g/h). This relatively high metabolic rate decreases down to 1.2-1.3 nl of O-2 during the endogenous peak in ecdysteroid concentration that culminates around pupariation. The metabolic decline coincides with the exocytosis of the proteinaceous glue. During and shortly after puparium formation, which is accompanied cytologically by intense vacuolation, O-2 consumption in the SG temporarily increases to 1.6 nl O-2/gland/min. After this time, the metabolic rate of the SG decreases downward steadily until 16 h APF, when the glands disintegrate and cease to consume oxygen. The SG we analyzed from Drosophila larvae were composed of 134 intrinsic cells, with the average volume of one lobe being 37 nl.
    WorkplaceBiology Centre (since 2006)
    ContactDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Year of Publishing2017
    Electronic addresshttp://www.sciencedirect.com/science/article/pii/S0022191015001328
Number of the records: 1  

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