scholarly journals THE CYTOLOGICAL EFFECT OF ECDYSTERONE ON THE MIDGUT CELLS OF THE FLESH-FLY SARCOPHAGA BULLATA

1971 ◽  
Vol 49 (3) ◽  
pp. 702-711 ◽  
Author(s):  
Sharon V. Radford ◽  
Donald W. Misch
Keyword(s):  
Epithelial Cells ◽  
Larval Instar ◽  
Cytological Effect ◽  
Flesh Fly ◽  
Sarcophaga Bullata ◽  
The Third ◽  
Secondary Lysosomes ◽  
Moulting Hormone

Larvae of the flesh-fly, Sarcophaga bullata, were injected with the synthetic moulting hormone ecdysterone or saline at the beginning of the third and final larval instar. One group was left untreated. The ecdysterone-injected larvae showed an increase in number of secondary lysosomes in the midgut epithelial cells similar to that observed at the onset of metamorphosis, an event which would normally occur about 48 hr later in these larvae.

scholarly journals CDC42 and Rac1 control different actin-dependent processes in the Drosophila wing disc epithelium.

1995 ◽  
Vol 131 (1) ◽  
pp. 151-164 ◽  
Author(s):  
S Eaton ◽  
P Auvinen ◽  
L Luo ◽  
Y N Jan ◽  
K Simons
Keyword(s):  
Epithelial Cells ◽  
Cell Shape ◽  
Larval Instar ◽  
Cell Types ◽  
Wing Disc ◽  
Dominant Negative ◽  
The Third ◽  
Drosophila Wing ◽  
Cell Shape Changes ◽  
Shape Changes

Cdc42 and Rac1 are members of the rho family of small guanosinetriphosphatases and are required for a diverse set of cytoskeleton-membrane interactions in different cell types. Here we show that these two proteins contribute differently to the organization of epithelial cells in the Drosophila wing imaginal disc. Drac1 is required to assemble actin at adherens junctions. Failure of adherens junction actin assembly in Drac1 dominant-negative mutants is associated with increased cell death. Dcdc42, on the other hand, is required for processes that involve polarized cell shape changes during both pupal and larval development. In the third larval instar, Dcdc42 is required for apico-basal epithelial elongation. Whereas normal wing disc epithelial cells increase in height more than twofold during the third instar, cells that express a dominant-negative version of Dcdc42 remain short and are abnormally shaped. Dcdc42 localizes to both apical and basal regions of the cell during these events, and mediates elongation, at least in part, by effecting a reorganization of the basal actin cytoskeleton. These observations suggest that a common cdc42-based mechanism may govern polarized cell shape changes in a wide variety of cell types.

scholarly journals Immunocytochemical localization of tissue kallikrein in brain ventricular epithelium and hypothalamic cell bodies.

1985 ◽  
Vol 33 (9) ◽  
pp. 951-953 ◽  
Author(s):  
J A Simson ◽  
R Dom ◽  
J Chao ◽  
C Woodley ◽  
L Chao ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Epithelial Cells ◽  
Third Ventricle ◽  
Immunoperoxidase Staining ◽  
Tissue Kallikrein ◽  
Immunocytochemical Localization ◽  
Specific Monoclonal Antibody ◽  
The Third ◽  
Indirect Immunoperoxidase ◽  
Rat Tissue

A specific monoclonal antibody against rat tissue kallikrein was used as the primary antibody for indirect immunoperoxidase staining of rat hypothalamus. Kallikrein was localized in the epithelial cells (ependyma) lining the third ventricle as well as in cell bodies of arcuate, supraoptic, paraventricular, and ventromedial nuclei.

The Post-embryonic Development of the Tracheal System in Drosophila melanogaster

1957 ◽  
Vol s3-98 (41) ◽  
pp. 123-150
Author(s):  
JOAN M. WHITTEN
Keyword(s):  
Drosophila Melanogaster ◽  
Adult Stage ◽  
Larval Instar ◽  
Pupal Stage ◽  
Tracheal System ◽  
True Nature ◽  
The Third ◽  
Air Sacs ◽  
Abdominal Region ◽  
Pupal Cuticle

The fate of the tracheal system is traced from the first larval instar to the adult stage. The basic larval pattern conforms to that shown for other Diptera Cyclorrhapha (Whitten, 1955), and is identical in all three instars. According to previous accounts the adult system directly replaces the larval: the larval system is partly shed, partly histolysed, and the adult system arises from imaginal cell clusters independently of the preceding larval system. In contrast, it is shown here that in the cephalic, thoracic, and anterior abdominal region there is a definite continuity in the tracheal system, from larval, through pupal to the adult stage, whereas in the posterior abdominal region the larval system is histolysed, and the adult system is independent of it in origin. Moreover, in the pupal stage this region is tracheated by tracheae arising from the anterior abdominal region and belonging to a distinct pupal system. Moulting of the tracheal linings is complete at the first and second larval ecdyses, but incomplete at the third larval-pupal and pupal-adult ecdyses. In consequence, in both pupal and adult systems there are tracheae which are secreted around preexisting tracheae, others formed as new ‘branch’ tracheae, and those which have been carried over from the previous instar. In the adult the newly formed tracheae of the posterior abdominal region fall into a fourth category. Most of the adult thoracic air sacs correspond to new ‘branch’ tracheae of other instars. The pre-pupal moult and instar are discussed with reference to the tracheal system and tentative suggestions are made concerning the true nature of the pre-pupal cuticle. There is no pre-pupal tracheal system. Events traced for Drosophila would seem to be general for Cyclorrhapha, both Acalypterae and Calypterae. The separate fates of the anterior and posterior abdom inal systems, in contrast with the straightforward development in Dipterc Nematocera, would appear to mark a distinct step in the evolution of the system in Diptera.

scholarly journals Production of germ-free mosquitoes via transient colonisation allows stage-specific investigation of host-microbiota interactions

2019 ◽  
Author(s):  
Ottavia Romoli ◽  
Johan Claes Schönbeck ◽  
Siegfried Hapfelmeier ◽  
Mathilde Gendrin
Keyword(s):  
Larval Development ◽  
Emerging Adults ◽  
Larval Instar ◽  
Bacterial Colonisation ◽  
Germ Free ◽  
Functional Studies ◽  
The Third ◽  
Novel Approach ◽  
Folate Biosynthesis ◽  
Vector Borne

AbstractThe mosquito microbiota impacts the physiology of its host and is essential for normal larval development, thereby influencing transmission of vector-borne pathogens. Germ-free mosquitoes generated with current methods show larval stunting and developmental deficits. Therefore, functional studies of the mosquito microbiota have so far mostly been limited to antibiotic treatments of emerging adults. In this study, we developed a novel approach to produce germ-free Aedes aegypti mosquitoes. It is based on reversible colonisation with bacteria genetically modified to allow complete decolonisation at any developmental stage. We show that, unlike germ-free mosquitoes previously produced using sterile diets, reversibly colonised mosquitoes show no developmental retardation and reach the same size as control adults. This allowed us to uncouple the study of the microbiota in larvae and adults. In adults, we detected no impact of bacterial colonisation on mosquito fecundity or longevity. In larvae, we performed a transcriptome analysis and diet supplementation experiments following decolonisation during the third larval instar. Our data suggest that bacteria support larval development by contributing to folate biosynthesis and by enhancing energy storage. Our study establishes a novel tool to study the microbiota in insects and deepens our knowledge on the metabolic contribution of bacteria to mosquito development.

scholarly journals Efficacy of Bacillus thuringiensis (Berliner) isolates on fig moth, Ephestia cautella (Walker) Larvae

2014 ◽  
Vol 11 (2) ◽  
pp. 943-951
Author(s):  
Baghdad Science Journal
Keyword(s):  
Bacillus Thuringiensis ◽  
Larval Stage ◽  
Filter Paper ◽  
Larval Instar ◽  
Ephestia Cautella ◽  
Larval Stages ◽  
The Third ◽  
Total Percentage ◽  
First Instar ◽  
Paper Method

The following dilution 5×10-1, 10-1, 10?2 , 10-3 gm/L for the indigenous isolate of Bacillus thuringiensis bacteria and the commercially isalate were used for experiments against the different stages of fig moth of E.cautella which exposed by filter paper method. The results showed that mortality of larval stages was increased with the increasing concentration of the biocide, in addition to increase in the mortality of the larval stages reached to the highest percentage in the third days of treatment of the larval stage in comparison with the first and second days of exposure. The results also showed that the sensitivity of larval stages was increased in first and second instars while reduced in the last instars .The high percentage of first instar mortality for the indigenous isolate in the concentration of 5×10-1 was 72.8% , while the low percentage of mortality showed in the concentration of 5×10-1 for the fifth instar larvae which was 13.3% in third days of treatment while a high percentage of mortality was showed for the first instar larvae for the commercially isulate in the concentration of 5×10-1 was 59.4% Furthermore, low percentage of mortality was shown in the concentration of 5×10-1 in fifth instar larval which was 8.3% in the third days of treatment. The results also showed that the indigenous isolated was more effective than the commercially produced bacteria for killing larval instars of fig moth E.cautella .The total percentage of larval instar mortality reached to 44.5 % after the third days of treatment in concentration 5×10-1 in the indigenous isolate , and it was 33.8 % in the commercially produced bacteria .

Photoperiodic control of development in the pitcher-plant mosquito, Wyeomyia smithii

1972 ◽  
Vol 50 (6) ◽  
pp. 713-719 ◽  
Author(s):  
William E. Bradshaw ◽  
L. Philip Lounibos
Keyword(s):  
Larval Instar ◽  
Pitcher Plant ◽  
Photoperiodic Control ◽  
Wyeomyia Smithii ◽  
Diapause Termination ◽  
Environmental Consequences ◽  
The Third ◽  
Short Day ◽  
Critical Daylength ◽  
Short Days

Wyeomyia smithii diapause in the third larval instar. Long days avert or terminate and short days promote or maintain diapause. Diapause occurs early in the third instar and may be terminated by photoperiodic stimuli without the intervention of chilling or other factors. Fifty percent termination of diapause requires about 3 long days and another [Formula: see text] days are consumed in the third instar for postdiapause development. The critical daylength is identical for both the initiation and termination of diapause, 14.75 h of light per day. But, the photoperiodic clock monitoring diapause decisions is several times as accurate during initiation as in termination, reflecting the more drastic environmental consequences of development misdirection in the fall than in the spring. This accuracy is further enhanced by a prolongation of the second instar under short-day conditions. The doubling in the duration of the second instar exhibits the same critical daylength properties as diapause determination.The third instar is divisible into four distinct developmental periods: prediapause, diapause, termination of diapause, and postdiapause. Methods for quantifying these periods are presented. Similar manipulations could be employed for other diapausing arthropods, regardless of the stage at which dormancy occurs or the cues used in its regulation.

Development and differentiation in vitro of Drosophila imaginal disc cells from dissociated early embryos

Development ◽  
1975 ◽  
Vol 33 (2) ◽  
pp. 487-498
Author(s):  
Andreas Dübendorfer ◽  
Glen Shields ◽  
James H. Sang
Keyword(s):  
Imaginal Disc ◽  
Larval Instar ◽  
Cell Types ◽  
The Third ◽  
Early Embryos ◽  
Disc Cells ◽  
Development And Differentiation ◽  
Pattern Specification

Embryos of Drosophila melanogaster, 6–8 h after oviposition, were dissociated and the cells cultured in vitro. Besides larval cell types, imaginal disc cells, assembled and growing in bloated monolayered vesicles, were obtained. The cells of these vesicles become competent to differentiate adult structures when treated with α-ecdysone or ecdysterone in vitro. Recognizable patterns of the adult fly are not formed though. If metamorphosis of imaginal cell vesicles from in vitro-cultures is induced in vivo by transplantation into host larvae of various ages within the third larval instar, recognizable patterns can differentiate provided the host larva does not metamorphose prior to 2 days after transplantation. The frequency of specific patterns in the implants can be increased by providing 9 days of culture in vivo (adult host flies) before metamorphosis. Passage through the third larval instar is not essential for these cells to produce identifiable patterns since culture in adult flies alone can achieve this. The quality of the differentiated pattern is not correlated with the extent of cell proliferation in the cultured tissues. The problem of pattern specification in vitro and in vivo is discussed.

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