The University of Southampton
University of Southampton Institutional Repository

Changes in the components of a nuclear inositide cycle during differentiation in murine erythroleukaemia cells

Changes in the components of a nuclear inositide cycle during differentiation in murine erythroleukaemia cells
Changes in the components of a nuclear inositide cycle during differentiation in murine erythroleukaemia cells
Differentiation of murine erythroleukaemia cells with the chemical agent DMSO leads to a cessation of proliferation and the production of a number of erythrocyte markers such as haemoglobin. We have previously demonstrated that activation of proliferation leads to an increase in the production of nuclear diacylglycerol (DAG). Here we demonstrate that differentiation leads to a decrease in the levels of nuclear DAG and the activity of the nuclear-associated phosphoinositidase C (PIC). The change in activity appears to be due to a decrease in the mass levels of the beta 1 isoform, as demonstrated by the use of isoform-specific antibodies. Moreover, the changes correlate with the cessation of proliferation and an increase in the number of cells in G1 phase of the cell cycle, rather than with the number of cells which have differentiated. Indeed, although treatment of the cells with phorbol 12-myristate 13-acetate (PMA) inhibits the differentiation programme as assessed by haemoglobin staining, it does not inhibit the number of cells blocking in G1 of the cell cycle or the changes in nuclear DAG or PIC activity. The possible involvement of this nuclear inositide cycle during progression through the cell cycle is discussed.
Animals Blotting, Western *Cell Differentiation Cell Nucleus/enzymology/*metabolism Diglycerides/*metabolism Dimethyl Sulfoxide/pharmacology Erythrocytes/cytology/*metabolism G1 Phase Hemoglobins/biosynthesis Leukemia, Erythroblastic, Acute Mice Phosphatidylinositol 4,5-Diphosphate Phosphatidylinositol Phosphates Phosphatidylinositols/metabolism Phosphoric Diester Hydrolases/*metabolism Tetradecanoylphorbol Acetate/pharmacology Tumor Cells, Cultured
0264-6021
63-67
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Letcher, A. J.
08f1eb2a-f4b2-4b38-aa51-3ac65762e3d3
Banfic, H. H.
9cc72c33-5632-4b10-a457-eae95a6aa61e
Rhee, S. G.
0f2b63da-34a7-4910-b00e-ec4b67c596dc
Irvine, R. F.
a8a94b1b-419c-4262-b745-eae1941ce145
Divecha, N.
5c2ad0f8-4ce7-405f-8a15-2fc4ab96d787
Letcher, A. J.
08f1eb2a-f4b2-4b38-aa51-3ac65762e3d3
Banfic, H. H.
9cc72c33-5632-4b10-a457-eae95a6aa61e
Rhee, S. G.
0f2b63da-34a7-4910-b00e-ec4b67c596dc
Irvine, R. F.
a8a94b1b-419c-4262-b745-eae1941ce145

Divecha, N., Letcher, A. J., Banfic, H. H., Rhee, S. G. and Irvine, R. F. (1995) Changes in the components of a nuclear inositide cycle during differentiation in murine erythroleukaemia cells. Biochemical Journal, 312 (1), 63-67. (doi:10.1042/bj3120063).

Record type: Article

Abstract

Differentiation of murine erythroleukaemia cells with the chemical agent DMSO leads to a cessation of proliferation and the production of a number of erythrocyte markers such as haemoglobin. We have previously demonstrated that activation of proliferation leads to an increase in the production of nuclear diacylglycerol (DAG). Here we demonstrate that differentiation leads to a decrease in the levels of nuclear DAG and the activity of the nuclear-associated phosphoinositidase C (PIC). The change in activity appears to be due to a decrease in the mass levels of the beta 1 isoform, as demonstrated by the use of isoform-specific antibodies. Moreover, the changes correlate with the cessation of proliferation and an increase in the number of cells in G1 phase of the cell cycle, rather than with the number of cells which have differentiated. Indeed, although treatment of the cells with phorbol 12-myristate 13-acetate (PMA) inhibits the differentiation programme as assessed by haemoglobin staining, it does not inhibit the number of cells blocking in G1 of the cell cycle or the changes in nuclear DAG or PIC activity. The possible involvement of this nuclear inositide cycle during progression through the cell cycle is discussed.

This record has no associated files available for download.

More information

Published date: 1995
Keywords: Animals Blotting, Western *Cell Differentiation Cell Nucleus/enzymology/*metabolism Diglycerides/*metabolism Dimethyl Sulfoxide/pharmacology Erythrocytes/cytology/*metabolism G1 Phase Hemoglobins/biosynthesis Leukemia, Erythroblastic, Acute Mice Phosphatidylinositol 4,5-Diphosphate Phosphatidylinositol Phosphates Phosphatidylinositols/metabolism Phosphoric Diester Hydrolases/*metabolism Tetradecanoylphorbol Acetate/pharmacology Tumor Cells, Cultured

Identifiers

Local EPrints ID: 480031
URI: http://eprints.soton.ac.uk/id/eprint/480031
ISSN: 0264-6021
PURE UUID: ed2a4cf8-0362-4168-ad2a-c71249c9078e

Catalogue record

Date deposited: 01 Aug 2023 16:37
Last modified: 17 Mar 2024 02:59

Export record

Altmetrics

Contributors

Author: N. Divecha
Author: A. J. Letcher
Author: H. H. Banfic
Author: S. G. Rhee
Author: R. F. Irvine

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×