Neuronal differentiation of chromaffin cells in vitro, induced by extremely low frequency magnetic fields or nerve growth factor: A histological and ultrastructural comparative study


Por: Feria-Velasco A., Castillo-Medina S., Verdugo-Díaz L., Castellanos E., Orozco-Suárez S., Sánchez-Gómez C., Drucker-Colín R.

Publicada: 1 ene 1998
Resumen:
The application of nerve growth factor (NGF) to primary adrenal medulla chromaffin cell cultures induces phenotypic changes characterized mainly by the presence of neurites. A similar effect has been seen when these cells are stimulated by extremely low frequency magnetic fields (ELFMF). In this study, newborn rat chromaffin cells were cultured and subjected to NGF or ELFMF in order to compare their histological and ultrastructural characteristics. Cells cultured in the presence of NGF developed cytoplasmic projections and their distal ends showed growth cones as well as filopodia. With scanning and transmission electron microscopy, an increased submembranous electron density was observed in the nuclei of cells as well as irregular, wavy neuritic projections with a moderate number of varicosities, as well as the prevalence of intermediate filaments among the cytoskeleton components. Cells stimulated with ELFMF presented straighter neuritic extensions with a greater number of varicosities. With the transmission electron microscope, numerous neurotubules were observed, both in the cell soma and in their neuritic extensions. In both groups, growth cones were clearly identified by their ultrastructural characteristics. The differences seen in the cytoskeleton of cells stimulated with NGF or ELFMF suggest differential stimulation mechanisms possibly determining the biochemical, electrophysiological, and morphological characteristics in both types of cell cultures.

Filiaciones:
Feria-Velasco A.:
 Div. Biotecnologia y Patol. Medio A., CIATEJ (SEP-CONACYT), Guadalajara, Jalisco, Mexico

Castillo-Medina S.:
 U. Invest. Medica Enferm. O., Hospital de Oncología, Ctro. Médico Nac. Siglo XXI, México, D.F., Mexico

Verdugo-Díaz L.:
 Departamento de Fisiología, Facultad de Medicina, Inst. de Fisiología Celular, México, D.F., Mexico

Castellanos E.:
 U. Invest. Medica Enferm. O., Hospital de Oncología, Ctro. Médico Nac. Siglo XXI, México, D.F., Mexico

Orozco-Suárez S.:
 U. Invest. Medica Enferm. N., Hospital de Especialidades, Ctro. Médico Nac. Siglo XXI, México, D.F., Mexico

Sánchez-Gómez C.:
 Depto. Biol. Desarrollo y T., Hosp. Inf. Mex. Dr. Federico Gomez, SSA, México, D.F., Mexico

Drucker-Colín R.:
 Departamento de Fisiología, Facultad de Medicina, Inst. de Fisiología Celular, México, D.F., Mexico

 Departamento de Neurociencias, Inst. de Fisiología Celular, UNAM, México, D.F., Mexico

 Depto. de Fisiología, Facultad de Medicina, UNAM, Apdo. Postal 70-250, 04510 México, D.F., Mexico
ISSN: 03604012
Editorial
WILEY-LISS, DIV JOHN WILEY & SONS INC, 111 RIVER ST, HOBOKEN, NJ 07030 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 53 Número: 5
Páginas: 569-582
WOS Id: 000075481900007
ID de PubMed: 9726428

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