Skip to content
2000
Volume 14, Issue 10
  • ISSN: 1871-5273
  • E-ISSN: 1996-3181

Abstract

Ouabain stimulates activation of various signaling cascades such as protein kinase B (Akt) and Extracellular-signaling-regulated kinase 1/2 (ERK 1/2) in various cell lines. Retinoic acid (RA) is commonly used to induce neuroblastoma differentiation in cultures. Upon RA administration, human neuroblastoma cell line, SK-N-SH demonstrated neurite extensions, which is an indicator of neuronal cell differentiation. Here we report that ouabaininduced signaling is altered under the action of 1 μM RA in human neuroblastoma SK-N-SH cells. RA increased the expression of p110α subunit of phosphoinositide 3-kinase (PI3K), Akt and β1 subunit of Na+/K+-ATPase. Ouabain activated Akt and ERK 1/2 in differentiated SK-N-SH cells; this effect was not observed in non-differentiated SK-N-SH cells. Long-term incubation of non-differentiated SK-N-SH with 1 μM ouabain led to a decrease in the number of cells; this effect was reduced in differentiated SK-N-SH cells. Taken together, these results suggest that ouabain leads to cell death in neuroblastoma cells rather than neuronal cells due to the different response to ouabain manifested by activation of Akt and ERK 1/2. Highlights RA increases the expression of p110α subunit of PI3K, Akt and β1 subunit of Na+/K+-ATPase Ouabain induces activation of Akt and ERK 1/2 in differentiated SK-N-SH cells but not in non-differentiated cells 1 μM ouabain leads to a decrease in the number of cells in non-differentiated SK-N-SH Reduction of ouabain-induced cell death in differentiated SK-N-SH

Loading

Article metrics loading...

/content/journals/cnsnddt/10.2174/1871527314666150821103008
2015-12-01
2025-10-12
Loading full text...

Full text loading...

/content/journals/cnsnddt/10.2174/1871527314666150821103008
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test