Bica Laura, Liddell Jeffrey R, Donnelly Paul S, Duncan Clare, Caragounis Aphrodite, Volitakis Irene, Paterson Brett M, Cappai Roberto, Grubman Alexandra, Camakaris James, Crouch Peter J, White Anthony R
Department of Pathology, The University of Melbourne, Melbourne, Victoria, Australia.
Bio21 Molecular Science and Biotechnology Institute, Parkville, Victoria, Australia ; School of Chemistry, The University of Melbourne, Melbourne, Victoria, Australia.
PLoS One. 2014 Feb 28;9(2):e90070. doi: 10.1371/journal.pone.0090070. eCollection 2014.
Abnormal biometal homeostasis is a central feature of many neurodegenerative disorders including Alzheimer's disease (AD), Parkinson's disease (PD), and motor neuron disease. Recent studies have shown that metal complexing compounds behaving as ionophores such as clioquinol and PBT2 have robust therapeutic activity in animal models of neurodegenerative disease; however, the mechanism of neuroprotective action remains unclear. These neuroprotective or neurogenerative processes may be related to the delivery or redistribution of biometals, such as copper and zinc, by metal ionophores. To investigate this further, we examined the effect of the bis(thiosemicarbazonato)-copper complex, Cu(II)(gtsm) on neuritogenesis and neurite elongation (neurogenerative outcomes) in PC12 neuronal-related cultures. We found that Cu(II)(gtsm) induced robust neurite elongation in PC12 cells when delivered at concentrations of 25 or 50 nM overnight. Analogous effects were observed with an alternative copper bis(thiosemicarbazonato) complex, Cu(II)(atsm), but at a higher concentration. Induction of neurite elongation by Cu(II)(gtsm) was restricted to neurites within the length range of 75-99 µm with a 2.3-fold increase in numbers of neurites in this length range with 50 nM Cu(II)(gtsm) treatment. The mechanism of neurogenerative action was investigated and revealed that Cu(II)(gtsm) inhibited cellular phosphatase activity. Treatment of cultures with 5 nM FK506 (calcineurin phosphatase inhibitor) resulted in analogous elongation of neurites compared to 50 nM Cu(II)(gtsm), suggesting a potential link between Cu(II)(gtsm)-mediated phosphatase inhibition and neurogenerative outcomes.
异常的生物金属稳态是包括阿尔茨海默病(AD)、帕金森病(PD)和运动神经元病在内的许多神经退行性疾病的核心特征。最近的研究表明,作为离子载体的金属络合化合物,如氯碘羟喹和PBT2,在神经退行性疾病的动物模型中具有强大的治疗活性;然而,神经保护作用的机制仍不清楚。这些神经保护或神经再生过程可能与金属离子载体对生物金属(如铜和锌)的递送或重新分布有关。为了进一步研究这一点,我们研究了双(硫代碳酰腙)铜配合物Cu(II)(gtsm)对PC12神经元相关培养物中神经突发生和神经突伸长(神经再生结果)的影响。我们发现,当以25或50 nM的浓度过夜递送时,Cu(II)(gtsm)可诱导PC12细胞中强大的神经突伸长。另一种双(硫代碳酰腙)铜配合物Cu(II)(atsm)也观察到了类似的效果,但浓度更高。Cu(II)(gtsm)诱导的神经突伸长仅限于长度在75-99 µm范围内的神经突,50 nM Cu(II)(gtsm)处理使该长度范围内的神经突数量增加了2.3倍。我们研究了神经再生作用的机制,发现Cu(II)(gtsm)抑制细胞磷酸酶活性。用5 nM FK506(钙调神经磷酸酶抑制剂)处理培养物,与50 nM Cu(II)(gtsm)相比,可导致类似的神经突伸长,这表明Cu(II)(gtsm)介导的磷酸酶抑制与神经再生结果之间可能存在联系。