Development of Dopaminergic Neurons from Neural Stem Cells and Transplantation Into a Neonatal and Adult Animal Model of Parkinson's Disease PDF Download
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Author: Torben Scholz
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Torben Scholz
Publisher:
ISBN:
Category :
Languages : en
Pages :
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Author: Lazaros C. Triarhou
Publisher: Springer Science & Business Media
ISBN: 1461506999
Category : Medical
Languages : en
Pages : 152
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Book Description
This book is the culmination of fifteen years of research on the transplantation of dopaminergic neurons in the striatum of the weaver mouse (wv/wv), a neurological mutant characterized by genetically-determined degeneration of midbrain dopamine neurons. This mutant constitutes the only available laboratory model with a chronic disorder that mimics Parkinson's disease. Structural and functional aspects of intrastriatal mesencephalic neuron grafting into the weaver model are reviewed, including histochemical correlates of graft survival and integration, numerical aspects of donor cell survival, ultrastructural findings on synaptogenesis, neurochemical indices of dopamine uptake and receptor binding, gene expression of structural and neurotransmitter-receptor related molecules, levels of striatal amino acid receptors, and behavioural effects of unilateral and bilateral neuronal transplantations.
Author: Jeroen Pasterkamp
Publisher: Springer Science & Business Media
ISBN: 1441903224
Category : Medical
Languages : en
Pages : 143
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Book Description
Theneurotransmitter dopamine has just celebrated its 50thbirthday. The discovery of dopamine as a neuronal entity in the late 1950s and the notion that it serves in neurotransmission has been a milestone in the field of neuroscience research. This milestone marked the beginning of an era that explored the brain as an integrated collection of neuronal systems that one could distinguish on basis of neurotransm- ter identities, and importantly, in which one started to be able to pinpoint the seat of brain disease. The mesodiencephalic dopaminergic (mdDA) system, previously designated as midbraindopaminergic system, has received much attention since its discovery. The initial identification of dopamine as a neurotransmitter in the central nervous system (CNS) and its relevance to psychiatric and neurological disorders have stimulated a plethora of neurochemical, pharmacological and genetic studies into the function of dopamine neurons and theirprojections. In the last decade, studies on gene expression and development have further increased the knowledge of this neuronal population and have unmasked a new level of complexity. The start of the molecular dissection of the mdDA system has been marked by the cloning and characterization ofNurrl and Pitx3. These transcription factors were shown to have a critical function during mdDA development. These initial studies have been followed by the identification of many other proteins, which have a crucial function in the creation of a dopamine neuron permissive region, induction of precursors, induction of terminaldifferent- tion and finally maintenance of the mdDA neuronal pool.
Author: Guido Nikkhah
Publisher:
ISBN:
Category : Parkinson's disease
Languages : en
Pages : 214
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Author: Lazaros Constantinos Triarhou
Publisher:
ISBN: 9780306474187
Category : Dopaminergic neurons
Languages : en
Pages : 148
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Book Description
"This book is the result of 15 years of research on the transplantation of dopaminergic neurons in the striatum of the weaver mouse, a neurological mutant characterized by genetically-determined degeneration of midbrain dopamine neurons."--V.
Author: Giuseppe di Giovanni
Publisher: Springer Science & Business Media
ISBN: 3211926607
Category : Medical
Languages : en
Pages : 357
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Book Description
This book provides a unique and timely multidisciplinary synthesis of our current knowledge of the anatomy, pharmacology, physiology and pathology of the substantia nigra pars compacta (SNc) dopaminergic neurons. The single chapters, written by top scientists in their fields, explore the life cycle of dopaminergic neurons from their birth to death, the cause of Parkinson's disease, the second most common and disabling condition in the elderly population. Nevertheless, the intracellular cascade of events leading to dopamine cell death is still unknown and, consequently, treatment is symptomatic rather than preventive. The mechanisms by which alterations cause neuronal death, new therapeutic approaches and the latest evidence of a possible de novo neurogenesis in the SNc are reviewed and singled out in different chapters. This book bridges basic science and clinical practice and will prepare the reader for the next few years, which will surely be eventful in terms of the progress of dopamine research.
Author: Lazaros Triarhou
Publisher: Springer
ISBN: 9781461507000
Category : Medical
Languages : en
Pages : 148
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Book Description
Author: William J. Freed
Publisher: MIT Press
ISBN: 9780262062084
Category : Central nervous system
Languages : en
Pages : 590
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Book Description
After providing basic background on transplantation, brain structure, and development, the book discusses Parkinson's disease, the use of transplants to influence localized brain functions, circuit reconstruction, and genetic engineering and other future technologies.
Author: Umberto Di Porzio
Publisher: Landes Bioscience
ISBN:
Category : Developmental neurobiology
Languages : en
Pages : 210
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Book Description
Author: Sarah Mantash
Publisher:
ISBN:
Category :
Languages : en
Pages : 0
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Book Description
Neurodegenerative diseases such as Parkinson's disease (PD) and traumatic brain injuries (TBI) are the most common causes of neural cell death and constitute a serious public health concern with hundreds of thousand people affected each year. In this way, many efforts are developed to understand the molecular and cellular bases of neurodegenerative processes and to devise effective therapies. Indeed, several surgery- or drug-based treatments have been postulated as therapeutic avenues for TBI and PD. For example, deep brain stimulation aims to relieve symptomatic complications in patients with PD and decompressive craniectomy can reduce the intracranial pressure after TBI. Pharmaceutical interventions in TBI include drugs that target secondary injury mechanisms. In PD, using dopamine agonists such as L-DOPA aims to compensate the dopaminergic (DA) loss in the striatum. However, these treatments are most often symptomatologic and do not completely re-establish the degenerated pathways or lost neurons. In this way, cell therapy is a promising avenue to restore disrupted pathways and replace lost neurons in PD and TBI. In this work, we studied molecular and cellular mechanisms of a cell therapy in mouse models of PD and TBI.In PD, fetal cell transplantations have been long considered as a promising therapeutic approach to restore the disrupted nigrostriatal dopaminergic connectivity which is initially established under the influence of multiple axon guidance cues. We and others previously showed that intranigral transplantation in adult mice model of PD, of fetal ventral mesencephalon cells collected from E12.5 mice embryos functionally and anatomically restores the motor deficits. In addition, we previously showed that Semaphorin7A (Sema7A) axon guidance molecule may be more particularly involved in this restoration since its expression increases after transplantation in several regions surrounding the nigrostriatal pathway. By this mean, we investigated the influence of Sema7A on the nigrostriatal pathway reconstruction in a mouse model of PD, toxically induced with 6-hydroxydopamine and after grafting with E12.5 ventral mesencephalon fetal cells. We also tested the influence of this axon guidance molecule in the establishment of this pathway during embryogenesis and in intact adult brain using Sema7A knock-out mice. We showed that Sema7A is necessary for the development of the DA neurons in the ventral mesencephalon during embryogenesis and is differentially expressed in the adult striatum, suggesting its implication in the mesostriatal DA topography. After fetal cell therapy in a mouse model of PD, we showed that Sema7A may play a role in the neuroinflammation processes described to decrease the survival of the grafted cells. These results bring new insights on the role of Sema7A in the development of DA neurons and for protective strategies of grafted cells in cell therapy approaches. Finally, we explored the whole proteome in nigrostriatal pathway-related regions in adults to test the influence of fetal cell transplantation on protein expression.Cortical brain injuries are also candidates for cell replacement strategies to ameliorate functional recovery and anatomical repair. Thus, as presented in the second part of this work, we assessed the effects of neural cell transplantation in a mild controlled cortical impact mouse model of TBI. We observed that implantation of embryonic neural stem cells or of differentiated cells decreases neuroinflammation and enhances neurogenesis following grafting. Moreover, association of neural stem cell transplantation with docosahexaenoic acid injections significantly attenuated TBI-induced motor function deficits and promoted neurogenesis.In conclusion, considering a combined therapeutic strategy by integrating cell transplantation protocols and targeting specific molecules involved in normal functioning of the neuronal circuitry, could ameliorate recovery in patients with PD and TBI.
