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The asymmetric cell division regulators par3, scribble and PINS/GPSM2 are not essential for erythroid development or enucleation

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posted on 2024-08-06, 10:35 authored by Christina B. Wölwer, Nathan Gödde, Luke B. Pase, Imogen A. Elsum, Krystle Y B Lim, Faruk Sacirbegovic, Carl R. Walkley, Sarah Ellis, Shigeo Ohno, Fumio Matsuzaki, Sarah RussellSarah Russell, Patrick O. Humbert
Erythroid enucleation is the process by which the future red blood cell disposes of its nucleus prior to entering the blood stream. This key event during red blood cell development has been likened to an asymmetric cell division (ACD), by which the enucleating erythroblast divides into two very different daughter cells of alternate molecular composition, a nucleated cell that will be removed by associated macrophages, and the reticulocyte that will mature to the definitive erythrocyte. Here we investigated gene expression of members of the Par, Scribble and Pins/Gpsm2 asymmetric cell division complexes in erythroid cells, and functionally tested their role in erythroid enucleation in vivo and ex vivo. Despite their roles in regulating ACD in other contexts, we found that these polarity regulators are not essential for erythroid enucleation, nor for erythroid development in vivo. Together our results put into question a role for cell polarity and asymmetric cell division in erythroid enucleation.

Funding

Japan Society for the Promotion of Science

National Health and Medical Research Council

Peter MacCallum Cancer Centre

History

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PDF (Published version)

ISSN

1932-6203

Journal title

PLoS ONE

Volume

12

Issue

1

Article number

article no. e0170295

Pagination

e0170295-

Publisher

Public Library of Science

Copyright statement

Copyright © 2017 Wolwer et al. This is an open access article distributed under the terms of the Creative Commons Attribution License.

Language

eng

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