Cargando…

Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo

The last stage of cell division involves two daughter cells remaining interconnected by a cytokinetic bridge that is cleaved during abscission. Conserved between the zebrafish embryo and human cells, we found that the oldest centrosome moves in a Rab11-dependent manner towards the cytokinetic bridge...

Descripción completa

Detalles Bibliográficos
Autores principales: Krishnan, Nikhila, Swoger, Maxx, Rathbun, Lindsay I, Fioramonti, Peter J, Freshour, Judy, Bates, Michael, Patteson, Alison E, Hehnly, Heidi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933627/
https://www.ncbi.nlm.nih.gov/pubmed/35304423
http://dx.doi.org/10.26508/lsa.202201362
_version_ 1784671696054124544
author Krishnan, Nikhila
Swoger, Maxx
Rathbun, Lindsay I
Fioramonti, Peter J
Freshour, Judy
Bates, Michael
Patteson, Alison E
Hehnly, Heidi
author_facet Krishnan, Nikhila
Swoger, Maxx
Rathbun, Lindsay I
Fioramonti, Peter J
Freshour, Judy
Bates, Michael
Patteson, Alison E
Hehnly, Heidi
author_sort Krishnan, Nikhila
collection PubMed
description The last stage of cell division involves two daughter cells remaining interconnected by a cytokinetic bridge that is cleaved during abscission. Conserved between the zebrafish embryo and human cells, we found that the oldest centrosome moves in a Rab11-dependent manner towards the cytokinetic bridge sometimes followed by the youngest. Rab11-endosomes are organized in a Rab11-GTP dependent manner at the mother centriole during pre-abscission, with Rab11 endosomes at the oldest centrosome being more mobile compared with the youngest. The GTPase activity of Rab11 is necessary for the centrosome protein, Pericentrin, to be enriched at the centrosome. Reduction in Pericentrin expression or optogenetic disruption of Rab11-endosome function inhibited both centrosome movement towards the cytokinetic bridge and abscission, resulting in daughter cells prone to being binucleated and/or having supernumerary centrosomes. These studies suggest that Rab11-endosomes contribute to centrosome function during pre-abscission by regulating Pericentrin organization resulting in appropriate centrosome movement towards the cytokinetic bridge and subsequent abscission.
format Online
Article
Text
id pubmed-8933627
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Life Science Alliance LLC
record_format MEDLINE/PubMed
spelling pubmed-89336272022-03-25 Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo Krishnan, Nikhila Swoger, Maxx Rathbun, Lindsay I Fioramonti, Peter J Freshour, Judy Bates, Michael Patteson, Alison E Hehnly, Heidi Life Sci Alliance Research Articles The last stage of cell division involves two daughter cells remaining interconnected by a cytokinetic bridge that is cleaved during abscission. Conserved between the zebrafish embryo and human cells, we found that the oldest centrosome moves in a Rab11-dependent manner towards the cytokinetic bridge sometimes followed by the youngest. Rab11-endosomes are organized in a Rab11-GTP dependent manner at the mother centriole during pre-abscission, with Rab11 endosomes at the oldest centrosome being more mobile compared with the youngest. The GTPase activity of Rab11 is necessary for the centrosome protein, Pericentrin, to be enriched at the centrosome. Reduction in Pericentrin expression or optogenetic disruption of Rab11-endosome function inhibited both centrosome movement towards the cytokinetic bridge and abscission, resulting in daughter cells prone to being binucleated and/or having supernumerary centrosomes. These studies suggest that Rab11-endosomes contribute to centrosome function during pre-abscission by regulating Pericentrin organization resulting in appropriate centrosome movement towards the cytokinetic bridge and subsequent abscission. Life Science Alliance LLC 2022-03-18 /pmc/articles/PMC8933627/ /pubmed/35304423 http://dx.doi.org/10.26508/lsa.202201362 Text en © 2022 Krishnan et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Krishnan, Nikhila
Swoger, Maxx
Rathbun, Lindsay I
Fioramonti, Peter J
Freshour, Judy
Bates, Michael
Patteson, Alison E
Hehnly, Heidi
Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
title Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
title_full Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
title_fullStr Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
title_full_unstemmed Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
title_short Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
title_sort rab11 endosomes and pericentrin coordinate centrosome movement during pre-abscission in vivo
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933627/
https://www.ncbi.nlm.nih.gov/pubmed/35304423
http://dx.doi.org/10.26508/lsa.202201362
work_keys_str_mv AT krishnannikhila rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT swogermaxx rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT rathbunlindsayi rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT fioramontipeterj rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT freshourjudy rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT batesmichael rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT pattesonalisone rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo
AT hehnlyheidi rab11endosomesandpericentrincoordinatecentrosomemovementduringpreabscissioninvivo