Subtype-specific neuronal differentiation of PC12 cells transfected with
2-adrenergic receptors
Authors: Taraviras S.1; Olli-Lähdesmäki T.2; Lymperopoulos A.1; Charitonidou D.1; Mavroidis M.1; Kallio J.2; Scheinin M.2; Flordellis C.1
Source: European Journal of Cell Biology, Volume 81, Number 6, 1 June 2002 , pp. 363-374(12)
Publisher: Urban & Fischer
Abstract:
Cells of the PC12 rat pheochromocytoma cell line acquire characteristics of sympathetic neurons under appropriate treatment. Stably transfected PC12 cells expressing individual
2-adrenergic receptor (
2-AR) subtypes were used to assess the role of
2-ARs in neuronal differentiation and to characterise the signalling pathways activated by the
2-AR agonist epinephrine in these cells. The effects of
2-AR activation were compared with the differentiating action and the signalling mechanisms of nerve growth factor (NGF). Epinephrine induced neuronal differentiation of PC12
2 cells through
2-AR activation in a subtype-dependent manner, internalization of all human
2-AR subtypes, and activation of mitogen-activated protein kinase (MAPK) and the serine-threonine protein kinase Akt. Epinephrine and NGF showed synergism in their differentiating effects. The MAPK kinase (MEK-1) inhibitor PD 98059 abolished the differentiating effect of epinephrine indicating that the differentiation is dependent on MAPK activation. Activating protein-1 (AP-1) DNA-binding activity was increased after epinephrine treatment in all three PC12
2 subtype clones. Evaluation of the potential physiological consequences of these findings requires further studies on endogenously expressed
2-ARs in neuronal cells.
Document Type: Research article
DOI: http://dx.doi.org/10.1078/0171-9335-00250
Affiliations: 1: Department of Pharmacology, School of Medicine, University of Patras, Rio Patras/Greece 2: Department of Pharmacology and Clinical Pharmacology, University of Turku, Turku/Finland
Publication date: 2002-06-01
- In this: publication
- By this: publisher
- In this Subject: Biology
- By this author: Taraviras S. ; Olli-Lähdesmäki T. ; Lymperopoulos A. ; Charitonidou D. ; Mavroidis M. ; Kallio J. ; Scheinin M. ; Flordellis C.

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