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Parkinson's disease (PD) is characterized by the progressive loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). In this study, we generated a transgenic model by crossing germline Parkin^–/–mice with PolgA^D257Amice, an established model of premature aging and mitochondrial stress. We hypothesized that loss of Parkin^–/–in PolgA^D257A/D257Amice would exacerbate mitochondrial dysfunction, leading to loss of dopamine neurons and nigral-striatal specific neurobehavioral motor dysfunction. We found that aged Parkin^–/–/PolgA^D257A/D257Amale and female mice exhibited severe behavioral deficits, nonspecific to the nigral-striatal pathway, with neither dopaminergic neurodegeneration nor reductions in striatal dopamine. We saw no difference in expression levels of nuclear-encoded subunits of mitochondrial markers and mitochondrial Complex I and IV activities, although we did observe substantial reductions in mitochondrial-encoded COX41I, indicating mitochondrial dysfunction as a result of PolgA^D257A/D257AmtDNA mutations. Expression levels of mitophagy markers LC3I/LC3II remained unchanged between cohorts, suggesting no overt mitophagy defects. Expression levels of the parkin substrates, VDAC, NLRP3, and AIMP2 remained unchanged, suggesting no parkin dysfunction. In summary, we were unable to observe dopaminergic neurodegeneration with corresponding nigral-striatal neurobehavioral deficits, nor Parkin or mitochondrial dysfunction in Parkin^–/–/PolgA^D257A/D257Amice. These findings support a lack of synergism of Parkin loss on mitochondrial dysfunction in mouse models of mitochondrial deficits.

SIGNIFICANCE STATEMENTProducing a mouse model of Parkinson's disease (PD) that is etiologically relevant, recapitulates clinical hallmarks, and exhibits reproducible results is crucial to understanding the underlying pathology and in developing disease-modifying therapies. Here, we show that Parkin^–/–/PolgA^D257A/D257Amice, a previously reported PD mouse model, fails to reproduce a Parkinsonian phenotype. We show that these mice do not display dopaminergic neurodegeneration nor nigral-striatal-dependent motor deficits. Furthermore, we report that Parkin loss does not synergize with mitochondrial dysfunction. Our results demonstrate that Parkin^–/–/PolgA^D257A/D257Amice are not a reliable model for PD and adds to a growing body of work demonstrating that Parkin loss does not synergize with mitochondrial dysfunction in mouse models of mitochondrial deficits.

 

The third industrial revolution has brought mankind into the information age. The development of information storage materials has played a key role in this transformation. Such materials have seen use in many application areas, including computing, logistics, and medicine. Information storage materials run the gamut from magnetic information storage media to molecular-based information storage materials. Among these, fluorescent-based information storage materials are of particular interest due to their unique properties, including an ability to store information with high levels of security, maintain mechanical stability, and respond to appropriately chosen external stimuli. In this review, we focus on recent advances involving the preparation and study of fluorescent materials-based information storage codes. For organisational purposes, these codes are treated according to the dimensionality of the code system in question, namely 1D-, 2D-, and 3D-type codes. The present review is designed to provide a succinct summary of what has been accomplished in the area, while outlining existing challenges and noting directions for future development.