• Something wrong with this record ?

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

R. Farkaš, K. Sláma,

. 2015 ; 81 (-) : 109-17. [pub] 20150625

Language English Country England, Great Britain

Document type Journal Article, Research Support, Non-U.S. Gov't

During 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 2μl) of tissue culture medium. The respiratory metabolism of single or up to 3 pairs of glands was evaluated by recording the rate of O2 consumption using a scanning microrespirographic technique sensitive to subnanoliter volumes of the respiratory O2 or CO2. The recordings were carried out at times between 8h before pupariation (BPF), until 16h APF, at which point the SG completely disintegrate. At the early wandering larval stage (8h BPF), the glands consume 2nl of O2/gland/min (=2500μl O2/g/h). This relatively high metabolic rate decreases down to 1.2-1.3nl of O2 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, O2 consumption in the SG temporarily increases to 1.6nl O2/gland/min. After this time, the metabolic rate of the SG decreases downward steadily until 16h 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 37nl. Therefore, a single SG cell of the wandering larva (with O2 consumption of 2nl/gland/min), consumes each about 16pl of O2/cell/min. A simultaneous analysis of the rate of protein and RNA synthesis in the SG shows a course similar to that found in respiratory metabolism.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16028407
003      
CZ-PrNML
005      
20200929094538.0
007      
ta
008      
161005s2015 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.jinsphys.2015.06.013 $2 doi
024    7_
$a 10.1016/j.jinsphys.2015.06.013 $2 doi
035    __
$a (PubMed)26116777
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Farkaš, Robert $u Laboratory of Developmental Genetics, Institute of Experimental Endocrinology, Slovak Academy of Sciences, Vlárska 3, 833 06 Bratislava, Slovakia. Electronic address: ueenfark@savba.sk.
245    10
$a Respiratory metabolism of salivary glands during the late larval and prepupal development of Drosophila melanogaster / $c R. Farkaš, K. Sláma,
520    9_
$a During 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 2μl) of tissue culture medium. The respiratory metabolism of single or up to 3 pairs of glands was evaluated by recording the rate of O2 consumption using a scanning microrespirographic technique sensitive to subnanoliter volumes of the respiratory O2 or CO2. The recordings were carried out at times between 8h before pupariation (BPF), until 16h APF, at which point the SG completely disintegrate. At the early wandering larval stage (8h BPF), the glands consume 2nl of O2/gland/min (=2500μl O2/g/h). This relatively high metabolic rate decreases down to 1.2-1.3nl of O2 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, O2 consumption in the SG temporarily increases to 1.6nl O2/gland/min. After this time, the metabolic rate of the SG decreases downward steadily until 16h 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 37nl. Therefore, a single SG cell of the wandering larva (with O2 consumption of 2nl/gland/min), consumes each about 16pl of O2/cell/min. A simultaneous analysis of the rate of protein and RNA synthesis in the SG shows a course similar to that found in respiratory metabolism.
650    _2
$a zvířata $7 D000818
650    _2
$a bazální metabolismus $7 D001481
650    _2
$a chromozomy hmyzu $7 D059006
650    _2
$a Drosophila melanogaster $x růst a vývoj $x metabolismus $7 D004331
650    _2
$a exocytóza $7 D005089
650    _2
$a larva $x růst a vývoj $x metabolismus $7 D007814
650    _2
$a biologická proměna $7 D008675
650    _2
$a spotřeba kyslíku $7 D010101
650    _2
$a slinné žlázy $x cytologie $x růst a vývoj $x metabolismus $7 D012469
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Sláma, Karel, $d 1934- $u Institute of Entomology, Czech Academy of Sciences, Drnovská 507, 161 00 Prague 6 - Ruzyně, Czech Republic. $7 jk01111779
773    0_
$w MED00006287 $t Journal of insect physiology $x 1879-1611 $g Roč. 81, č. - (2015), s. 109-17
856    41
$u https://pubmed.ncbi.nlm.nih.gov/26116777 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20161005 $b ABA008
991    __
$a 20200929094535 $b ABA008
999    __
$a ok $b bmc $g 1166721 $s 953037
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 81 $c - $d 109-17 $e 20150625 $i 1879-1611 $m Journal of insect physiology $n J Insect Physiol $x MED00006287
LZP    __
$a Pubmed-20161005

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...