Defining the role of cytoskeletal components in the formation of apoptopodia and apoptotic bodies during apoptosis.
Actins
/ metabolism
Animals
Apoptosis
/ drug effects
Cell Culture Techniques
Cell Membrane
/ drug effects
Cell Surface Extensions
/ drug effects
Cells, Cultured
Connexins
/ genetics
Cytoskeleton
/ metabolism
Epithelial Cells
/ cytology
Extracellular Vesicles
/ genetics
Female
Humans
Jurkat Cells
Male
Mice
Mice, Inbred C57BL
Microtubules
/ metabolism
Monocytes
/ cytology
Nerve Tissue Proteins
/ genetics
T-Lymphocytes
/ cytology
Tubulin
/ genetics
Vimentin
/ genetics
Apoptopodia
Apoptotic bodies
Apoptotic cell disassembly
Apoptotic morphology
Cytoskeletal components
Membrane protrusions
Journal
Apoptosis : an international journal on programmed cell death
ISSN: 1573-675X
Titre abrégé: Apoptosis
Pays: Netherlands
ID NLM: 9712129
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
pubmed:
7
9
2019
medline:
4
8
2020
entrez:
7
9
2019
Statut:
ppublish
Résumé
During apoptosis, dying cells undergo dynamic morphological changes that ultimately lead to their disassembly into fragments called apoptotic bodies (ApoBDs). Reorganisation of the cytoskeletal structures is key in driving various apoptotic morphologies, including the loss of cell adhesion and membrane bleb formation. However, whether cytoskeletal components are also involved in morphological changes that occur later during apoptosis, such as the recently described generation of thin apoptotic membrane protrusions called apoptopodia and subsequent ApoBD formation, is not well defined. Through monitoring the progression of apoptosis by confocal microscopy, specifically focusing on the apoptopodia formation step, we characterised the presence of F-actin and microtubules in a subset of apoptopodia generated by T cells and monocytes. Interestingly, targeting actin polymerisation and microtubule assembly pharmacologically had no major effect on apoptopodia formation. These data demonstrate apoptopodia as a novel type of membrane protrusion that could be formed in the absence of actin polymerisation and microtubule assembly.
Identifiants
pubmed: 31489517
doi: 10.1007/s10495-019-01565-5
pii: 10.1007/s10495-019-01565-5
doi:
Substances chimiques
Actins
0
Connexins
0
Nerve Tissue Proteins
0
PANX1 protein, human
0
Panx1 protein, mouse
0
Tubulin
0
Vimentin
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
862-877Subventions
Organisme : National Health and Medical Research Council (AU)
ID : GNT1125033
Pays : International
Organisme : National Health and Medical Research Council (AU)
ID : GNT1140187
Pays : International
Organisme : National Health and Medical Research Council (AU)
ID : GNT1141732
Pays : International
Organisme : Australian Research Council
ID : DP170103790
Pays : International
Commentaires et corrections
Type : ErratumIn