Dopamine and Cu+/2+ can induce oligomerization of α‐synuclein in the absence of oxygen: Two types of oligomerization mechanisms for α‐synuclein and related cell toxicity studies. Issue 3 (29th November 2013)
- Record Type:
- Journal Article
- Title:
- Dopamine and Cu+/2+ can induce oligomerization of α‐synuclein in the absence of oxygen: Two types of oligomerization mechanisms for α‐synuclein and related cell toxicity studies. Issue 3 (29th November 2013)
- Main Title:
- Dopamine and Cu+/2+ can induce oligomerization of α‐synuclein in the absence of oxygen: Two types of oligomerization mechanisms for α‐synuclein and related cell toxicity studies
- Authors:
- Ha, Yonghwang
Yang, Aerin
Lee, Seyoung
Kim, Kibong
Liew, Hyunjeong
Lee, Sang Hyung
Lee, Ju Eun
Lee, Hong‐In
Suh, Yoo‐Hun
Park, Hee‐Sung
Churchill, David G. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>α‐Synuclein oligomers can induce neurotoxicity and are implicated in Parkinson's disease etiology and disease progression. Many studies have reported α‐synuclein oligomerization by dopamine (DA) and transition metal ions, but few studies provide insight into joint influences of DA and Cu<sup>2+</sup>. In this study, DA and Cu<sup>2+</sup> were coadministered aerobically to measure α‐synuclein oligomerization under these conditions. In the presence of oxygen, DA induced α‐synuclein oligomerization in a dose‐dependent manner. Cu<sup>+/2+</sup> did not effect oligomerization in such a manner in the presence of DA. By electrophoresis, Cu<sup>2+</sup> was found easily to induce oligomerization with DA. This implies that oligomerization invoked by DA is reversible in the presence of Cu<sup>2+</sup>, which appears to be mediated by noncovalent bond interactions. In the absence of oxygen, DA induced less oligomerization of α‐synuclein, whereas DA/Cu<sup>2+</sup> induced aerobic‐level amounts of oligomers, suggesting that DA/Cu<sup>2+</sup> induces oligomerization independent of oxygen concentration. Radical species were detected through electron paramagnetic resonance (EPR) spectroscopic analysis arising from coincubation of DA/Cu<sup>2+</sup> with α‐synuclein. Redox reactions induced by DA/Cu<sup>2+</sup> were observed in multimer regions of α‐synuclein oligomers through NBT assay. Cellular<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>α‐Synuclein oligomers can induce neurotoxicity and are implicated in Parkinson's disease etiology and disease progression. Many studies have reported α‐synuclein oligomerization by dopamine (DA) and transition metal ions, but few studies provide insight into joint influences of DA and Cu<sup>2+</sup>. In this study, DA and Cu<sup>2+</sup> were coadministered aerobically to measure α‐synuclein oligomerization under these conditions. In the presence of oxygen, DA induced α‐synuclein oligomerization in a dose‐dependent manner. Cu<sup>+/2+</sup> did not effect oligomerization in such a manner in the presence of DA. By electrophoresis, Cu<sup>2+</sup> was found easily to induce oligomerization with DA. This implies that oligomerization invoked by DA is reversible in the presence of Cu<sup>2+</sup>, which appears to be mediated by noncovalent bond interactions. In the absence of oxygen, DA induced less oligomerization of α‐synuclein, whereas DA/Cu<sup>2+</sup> induced aerobic‐level amounts of oligomers, suggesting that DA/Cu<sup>2+</sup> induces oligomerization independent of oxygen concentration. Radical species were detected through electron paramagnetic resonance (EPR) spectroscopic analysis arising from coincubation of DA/Cu<sup>2+</sup> with α‐synuclein. Redox reactions induced by DA/Cu<sup>2+</sup> were observed in multimer regions of α‐synuclein oligomers through NBT assay. Cellular toxicity results confirm that, for normal and hypoxic conditions, copper or DA/Cu<sup>2+</sup> can induce cell death, which may arise from copper redox chemistry. From these results, we propose that DA and DA/Cu<sup>2+</sup> induce different mechanisms of α‐synuclein oligomerization, cross‐linking with noncovalent (or reversible covalent) bonding vs. likely radical‐mediated covalent modification. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Journal of neuroscience research. Volume 92:Issue 3(2014:Mar.)
- Journal:
- Journal of neuroscience research
- Issue:
- Volume 92:Issue 3(2014:Mar.)
- Issue Display:
- Volume 92, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 92
- Issue:
- 3
- Issue Sort Value:
- 2014-0092-0003-0000
- Page Start:
- 359
- Page End:
- 368
- Publication Date:
- 2013-11-29
- Subjects:
- Neurobiology -- Periodicals
612 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4547 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/109668564 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jnr.23323 ↗
- Languages:
- English
- ISSNs:
- 0360-4012
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5022.090000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3870.xml