Journal home
Advance online publication
Current issue
Archive
Press releases
Supplements and Focuses
Image gallery
Guide to authors
Online submissionOnline submission
Permissions
For referees
Free online issue
Contact the journal
Subscribe
Advertising
work@npg
naturereprints
About this site
For librarians
 
NPG Resources
Nature
Nature Reviews Molecular Cell Biology
UCSD-Nature Signaling Gateway
The Cell Migration Gateway
Nature Reports Stem Cells
Nature Reports Avian Flu
NPG Subject areas
Biotechnology
Cancer
Chemistry
Clinical Medicine
Dentistry
Development
Drug Discovery
Earth Sciences
Evolution & Ecology
Genetics
Immunology
Materials Science
Medical Research
Microbiology
Molecular Cell Biology
Neuroscience
Pharmacology
Physics
Browse all publications
Brief Communication
Nature Cell Biology  3, 918 - 921 (2001)
Published online: 12 September 2001; | doi:10.1038/ncb1001-918


There is a Correction (November 2001) associated with this Brief Communication.

There is an Erratum (November 2001) associated with this Brief Communication.

Extracellular control of cell size

Ian J. Conlon1, Graham A. Dunn2, Anne W. Mudge1 & Martin C. Raff1

1  MRC Laboratory for Molecular Cell Biology and the Biology Department, University College London, London WC1E 6BT, UK

2  MRC Muscle and Cell Motility Unit, The Randall Centre, New Hunt's House, Guy's Campus, London SE1 1UL, UK

Correspondence should be addressed to Ian J. Conlon i.conlon@ucl.ac.uk
Both cell growth (cell mass increase) and progression through the cell division cycle are required for sustained cell proliferation1. Proliferating cells in culture tend to double in mass before each division2, but it is not known how growth and division rates are co-ordinated to ensure that cell size is maintained1, 3, 4, 5. The prevailing view is that coordination is achieved because cell growth is rate-limiting for cell-cycle progression6, 7, 8, 9, 10. Here, we challenge this view. We have investigated the relationship between cell growth and cell-cycle progression in purified rat Schwann cells, using two extracellular signal proteins that are known to influence these cells11, 12, 13. We find that glial growth factor (GGF) can stimulate cell-cycle progression without promoting cell growth. We have used this restricted action of GGF to show that, for cultured Schwann cells, cell growth rate alone does not determine the rate of cell-cycle progression and that cell size at division is variable and depends on the concentrations of extracellular signal proteins that stimulate cell-cycle progression, cell growth, or both.


MORE ARTICLES LIKE THIS
These links to content published by NPG are automatically generated

REFERENCE
Oligodendrocytes
Nature Encyclopaedia of Life Sciences

RESEARCH
Overexpression of activated neu/erbB2 initiates immortalization and malignant transformation of immature Schwann cells in vitro
Oncogene Original Article (25 Nov 1999)
A Schwann cell mitogen accompanying regeneration of motor neurons
Nature Letters to Editor (11 Dec 1997)
Disruption of ErbB receptor signaling in adult non-myelinating Schwann cells causes progressive sensory loss
Nature Neuroscience Article (01 Nov 2003)

 Top
Abstract
Previous | Next
Table of contents
Full textFull text
Download PDFDownload PDF
Send to a friendSend to a friend
Save this linkSave this link

naturejobs

Figures & Tables
Supplementary info
Export citation
natureproducts

Search buyers guide:

 
ADVERTISEMENT
 
Nature Cell Biology
ISSN: 1465-7392
EISSN: 1476-4679
Journal home | Advance online publication | Current issue | Archive | Press releases | For authors | Online submission | For referees | Free online issue | About the journal | Contact the journal | Subscribe | Advertising | work@npg | Reprints and permissions | About this site | For librarians
Nature Publishing Group, publisher of Nature, and other science journals and reference works©2001 Nature Publishing Group | Privacy policy