Down Modulation of N-myc, Heat-Shock Protein 70, and Nucleolin during the Differentiation of Human Neuroblastoma Cells

Cultured human neuroblastoma (GOTO) cells were induced to differentiate by dibutyryl cyclic AMP (Bt2cAMP) and/or retinoic acid (RA). A combination of BtjcAMP (1 mM) and RA (1 μM) yielded the most significant networks of neurites after 3 to 4 days, this being associated with the reduction of N-myc mR...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of biochemistry (Tokyo) 1991-07, Vol.110 (1), p.146-150
Hauptverfasser: Murakami, Tadamasa, Ohmori, Hisamitsu, Gotoh, Sadao, Tsuda, Tohru, Ohya, Ryoichi, Akiya, Shinobu, Higashi, Ken
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Cultured human neuroblastoma (GOTO) cells were induced to differentiate by dibutyryl cyclic AMP (Bt2cAMP) and/or retinoic acid (RA). A combination of BtjcAMP (1 mM) and RA (1 μM) yielded the most significant networks of neurites after 3 to 4 days, this being associated with the reduction of N-myc mRNA levels. Next, we examined several cellular genes that were possibly linked with changes in N-myc gene expression under these conditions. Among the genes examined, both nucleolin and a major heat-shock protein (hsp70) mRNA8 showed changes concomitant with those in N-myc mRNA levels when induced by Bt2cAMP and RA. Dibutyryl cAMP alone induced several short cellular processes and caused a marked decrease in N-myc mRNA within 2 days. RA alone induced a few long and straight neurites along the longitudinal axis of individual cells and a significant decrease in growth rate but showed neither network formation nor a decrease in N-myc gene expression. These results indicate differential effects of Bt2cAMP and RA on the regulatory mechanisms of both cell proliferation and differentiation and also indicate a possible association of expression of N-myc gene with those of hsp70 and nucleolin genes.
ISSN:0021-924X
1756-2651
DOI:10.1093/oxfordjournals.jbchem.a123533