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Cancer Cell death Cell cycle Cytoskeleton Exo/endocytosis Differentiation Division Organelles Signalling Stem cells Trafficking
Cell Biology International (2004) 28, 273–279 (Printed in Great Britain)
Differentiation of chromaffin cells elicited by ELF MF modifies gene expression pattern
Tatiana Olivares‑Bañuelosa, Luz Navarrob, Alicia Gonzáleza and Rene Drucker‑Colı́na*
aDepartamento de Neurociencias, Instituto de Fisiologı́a Celular, Universidad Nacional Autónoma de México, Apartado Postal 70-600, México, D.F. 04510, Mexico
bDepartamento de Fisiologı́a, Facultad de Medicina, Universidad Nacional Autónoma de México, Apartado Postal 70-250, México, D.F. 04510, Mexico


Abstract

Chromaffin cells exposed to extremely low frequency magnetic fields (ELF MF, 60 Hz, 0.7 mT) differentiate into sympathetic neuron-like cells. This complex process must involve both qualitative and quantitative variations in gene expression. This study looks at whether ELF MF treatment provokes changes in the global transcription profile of chromaffin cells, using the RT-Differential Display method. When the gene expression patterns of experimental groups (nerve growth factor (NGF) and ELF MF) were compared to those receiving no treatment, at least 53 transcripts showing differential expression were detected. Eight RT–PCR products, corresponding to six genes, were re-amplified, sequenced and compared with the rat gene bank. Sequence analysis showed that these genes most likely encode: phosphoglucomutase-1, neurofibromatosis-2 interacting protein, microtubule associated protein-2, thiamine pyrophosphokinase, and two unidentified hypothetical proteins (RNOR02022103 and ROR01044577), and that the presumed regulatory regions of these genes contained CTCT-clusters, which are thought to be required for electromagnetic field-dependent gene expression.


Key words: ELF MF, Differential display, Chromaffin cells, NGF.

*Corresponding author. Tel.: +52-5-550-6662; fax: +52-5-550-0904


Received 14 August 2003/11 December 2003; accepted 20 January 2004

doi:10.1016/j.cellbi.2004.01.002


ISSN Print: 1065-6995
ISSN Electronic: 1095-8355
Published by Portland Press Limited on behalf of the International Federation for Cell Biology (IFCB)