Mechanisms of programmed cell death in the midgut and salivary glands from Bradysia hygida (Diptera: Sciaridae) during pupal-adult metamorphosis.
Bradysia hygida
apoptosis
autophagy
development
midgut
salivary glands
Journal
Cell biology international
ISSN: 1095-8355
Titre abrégé: Cell Biol Int
Pays: England
ID NLM: 9307129
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
18
02
2020
revised:
19
05
2020
accepted:
02
06
2020
pubmed:
5
6
2020
medline:
11
8
2021
entrez:
5
6
2020
Statut:
ppublish
Résumé
Programmed cell death is involved with the degeneration/remodeling of larval tissues and organs during holometabolous development. The midgut is a model to study the types of programmed cell death associated with metamorphosis because its structure while degenerating is a substrate for the formation of the adult organ. Another model is the salivary glands from dipteran because their elimination involves different cell death modes. This study aimed to investigate the models of programmed cell death operating during midgut replacement and salivary gland histolysis in Bradysia hygida. We carried out experiments of real-time observations, morphological analysis, glycogen detection, filamentous-actin localization, and nuclear acridine orange staining. Our findings allow us to establish that an intact actin cytoskeleton is required for midgut replacement in B. hygida and nuclear condensation and acridine orange staining precede the death of the larval cells. Salivary glands in histolysis present cytoplasmic blebbing, nuclear retraction, and acridine orange staining. This process can be partially reproduced in vitro. We propose that the larval midgut death involves autophagic and apoptotic features and apoptosis is a mechanism involved with salivary gland histolysis.
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1981-1990Subventions
Organisme : Fundação Araucária de Apoio Científico e Tecnológico do Paraná
ID : 5/2006
Informations de copyright
© 2020 International Federation for Cell Biology.
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