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Functional Neural Transplantation IV: Translation to Clinical Application, Part B, Volume 231 [Kõva köide]

Volume editor (Cardiff University, Cardiff, UK), Volume editor (Lund University, Lund, Sweden)
  • Formaat: Hardback, 316 pages, kõrgus x laius: 235x191 mm, kaal: 810 g
  • Sari: Progress in Brain Research
  • Ilmumisaeg: 26-May-2017
  • Kirjastus: Academic Press Inc
  • ISBN-10: 0128138793
  • ISBN-13: 9780128138793
Teised raamatud teemal:
  • Formaat: Hardback, 316 pages, kõrgus x laius: 235x191 mm, kaal: 810 g
  • Sari: Progress in Brain Research
  • Ilmumisaeg: 26-May-2017
  • Kirjastus: Academic Press Inc
  • ISBN-10: 0128138793
  • ISBN-13: 9780128138793
Teised raamatud teemal:

Functional Neural Transplantation IV: Translation to Clinical Application, Part B, Volume 231 provides the current status of cell transplantation in the nervous system, focusing on the conditions for achieving structural repair and functional recovery. New to this edition are chapters on Plasticity and Regeneration in the Injured Spinal Cord After Cell Transplantation Therapy, Transplantation of GABAergic Interneurons for Cell-Based Therapy, Rebuilding CNS Inhibitory Circuits to Control Chronic Neuropathic Pain and Itch, From Transplanting Schwann Cells in Experimental Rat Spinal Cord Injury to their Transplantation into Human Injured Spinal Cord in Clinical Trials, and the Recruitment of Endogenous CNS Stem Cells for Regeneration in Demyelinating Disease.

As the fourth in a periodic series of updates at 5-7 year intervals, this volume highlights recent developments in cellular and molecular science, providing the fundamental principles of neuroplasticity and regeneration in the brain and spinal cord, while also addressing the power of pluripotent stem cells to generate new sources of precisely specified neurons for utilization in brain repair.

  • Provides a comprehensive set of critical reviews covering the field
  • Presents state-of-the-art topics in science and translational medicine
  • Written by international leaders in the field of neural transplantation

Muu info

Focuses on the conditions for achieving structural repair and functional recovery after brain damage or neurodegenerative disease
Contributors v
Preface xxv
Chapter 1 Stem cell transplantation for spinal cord injury repair
1(32)
Paul Lu
1 Introduction
1(2)
2 MSCs for SCI Repair
3(2)
2.1 Sources of MSCs
3(1)
2.2 Mechanism of MSC Transplant for SCI Repair
3(1)
2.3 Neuronal Differentiation Potential of MSCs
4(1)
2.4 Clinical Trials of MSCs for SCI
4(1)
3 NSCs for SCI Repair
5(15)
3.1 Sources of NSCs and Their Differentiation Potential
5(5)
3.2 NSCs or NPCs for Neural Protection and Remyelination
10(1)
3.3 Axonal Growth and Connectivity From NSC Graft
11(6)
3.4 Host Axonal Regeneration and Connectivity With NSC Grafts
17(2)
3.5 Functional Outcomes
19(1)
4 Future Perspective
20(13)
Acknowledgments
22(1)
References
22(11)
Chapter 2 Plasticity and regeneration in the injured spinal cord after cell transplantation therapy
33(24)
Satoshi Nori
Masaya Nakamura
Hideyuki Okano
1 Introduction
33(2)
2 Optimal Timing of Cell Transplantation and Plasticity After SCI
35(1)
3 Cell Transplantation for Neural Regeneration and Plasticity
36(6)
3.1 Neural Stem/Progenitor Cells
36(1)
3.2 Embryonic Stem Cell-Derived Neural Stem Cells
37(1)
3.3 iPSC-Derived NSPCs
38(2)
3.4 Mesenchymal Stromal Cells
40(1)
3.5 Olfactory Ensheathing Cells
41(1)
3.6 Schwann Cells
41(1)
4 Plasticity and Regeneration After Cell Transplantation Therapy
42(5)
4.1 Remyelination
42(2)
4.2 Reconstruction of Neural Circuits
44(1)
4.3 Neurotrophic Support
45(2)
5 Conclusions
47(10)
Acknowledgments
48(1)
References
48(9)
Chapter 3 Transplantation of GABAergic interneurons for cell-based therapy
57(30)
Julien Spatazza
Waiter R. Mancia Leon
Arturo Alvarez-Buylla
1 Introduction
57(1)
2 Development of Telencephalic GABAergic Interneurons
58(2)
2.1 Tangential Migration
58(1)
2.2 Origins and Diversity
59(1)
3 Transplantation and the Study of Brain Development
60(6)
3.1 Intemeuron Intrinsic Developmental Program
61(3)
3.2 Intemeuron Fate and Survival
64(2)
4 Transplantation and Cortical Plasticity
66(3)
5 Disease-modifying Properties of MGE Transplants
69(5)
5.1 Schizophrenia
69(1)
5.2 Epilepsy
70(2)
5.3 Parkinson's Disease
72(1)
5.4 Alzheimer's Disease
72(1)
5.5 Neuropathic Pain
73(1)
6 Conclusion
74(13)
Acknowledgments
75(1)
References
75(12)
Chapter 4 Rebuilding CNS inhibitory circuits to control chronic neuropathic pain and itch
87(20)
Joao M. Braz
Alex Etlin
Dina Juarez-Salinas
Ida J. Llewellyn-Smith
Allan I. Basbaum
1 Introduction
87(2)
2 Medial Ganglionic Eminence-Derived Inhibitory Interneurons
89(1)
3 MGE Cell Transplants to Treat Neuropathic Pain
89(8)
3.1 MGE Cells Ameliorate Neuropathic Pain
91(2)
3.2 MGE Cells Integrate Extensively Into Host Spinal Cord Circuitry
93(1)
3.3 Functional and Anatomical Evidence for Synaptic Connectivity of Transplanted MGE Cells
94(2)
3.4 Is There an Endogenous GABAstat That Regulates MGE-Derived Inhibitory Control?
96(1)
3.5 MGE Cells Prevent the Development of Mechanical Allodynia
97(1)
4 Cell Transplants for the Management of Chronic Itch
97(3)
4.1 MGE Cells Reduce Spontaneous Scratching and Resolve Skin Lesions in Bhlhb5 Mutant Mice
98(1)
4.2 MGE Transplants Are Also Effective Against Chronic, Inflammatory Itch
98(2)
5 Translating Preclinical Transplantation Studies to the Clinic
100(1)
6 Conclusions
100(7)
References
101(6)
Chapter 5 From transplanting Schwann cells in experimental rat spinal cord injury to their transplantation into human injured spinal cord in clinical trials
107(28)
Mary B. Bunge
Paula V. Monje
Aisha Khan
Patrick M. Wood
1 Introduction
108(1)
2 Advantages of Primary SCs for Cell Therapy in SCI
108(2)
3 SC Proliferation: Cues for Achieving Expansion by Using Heregulin and cAMP-Stimulating Agents
110(1)
4 Other Sources of SCs
111(1)
5 SC Transplantation Studies in Rat SCI Models
112(1)
6 Development of the Clinically Relevant Protocol for Manufacturing Autologous Human SCs
113(9)
6.1 Making SCs Proliferate in Culture
114(1)
6.2 The Brockes Protocol: Fibroblast Depletion to Purify SC Cultures
114(1)
6.3 The Porter Protocol: Elimination of Cholera Toxin and Modification of the Culture Substratum
115(1)
6.4 Transformation of SCs With Extended Passages
116(1)
6.5 The Challenge of Isolating SCs From Adult Rat Nerve
116(1)
6.6 The Morrissey-Kleitman Protocol: Increasing Adult SC Expansion by Using Multiple Replating of Nerve Explants and Delayed Explant Dissociation
117(1)
6.7 The Morrissey-Kleitman-Levi Protocol: Replacement of GGF with Recombinant Heregulin and Addition of Cholera Toxin Back Into the Mitogenic Cocktail
118(1)
6.8 The Casella Protocol: Delayed Dissociation, Culture on Laminin, and Elimination of Cholera Toxin
119(2)
6.9 The Athauda Protocol: Manufacture of a Clinical Grade Human SC Product
121(1)
7 Clinical Research for Spinal Cord Injury
122(5)
7.1 Preclinical Studies to Gain EDA Approval for a SC Trial
123(1)
7.2 Regulatory Requirements to Manufacture SCs for Trials
124(1)
7.3 The First SC Clinical Trial at the Miami Project
125(1)
7.4 SC Processing and Transport to the Transplantation Site
126(1)
7.5 Trial Outcomes
126(1)
7.6 The Next Trial
126(1)
7.7 Next Steps in SC Manufacture and Quality Assurance
127(1)
8 Conclusion
127(8)
Acknowledgments
127(1)
References
128(7)
Chapter 6 Recruitment of endogenous CNS stem cells for regeneration in demyelinating disease
135(30)
Natalia A. Murphy
Robin J.M. Franklin
1 Introduction
135(1)
2 Overview: Myelination and Remyelination
136(3)
2.1 The Myelinated CNS: An Evolutionary Milestone
136(1)
2.2 Developmental Myelination
136(1)
2.3 The OPC
136(1)
2.4 Remyelination: The Default Response to a Demyelinating Insult
137(2)
3 Demyelination
139(3)
3.1 Myelin Disorders
139(1)
3.2 Consequences of Demyelination
140(1)
3.3 Acquired Demyelinating Disorders
140(1)
3.4 Experimental Models of Demyelination
140(2)
4 Failure of Remyelination
142(4)
4.1 Why Does Remyelination Fail?
142(1)
4.2 At What Stage Does Remyelination Fail?
142(1)
4.3 Remyelination Failure: Intrinsic Properties of Remyelinating Cells vs Extrinsic Properties of the Environment
143(2)
4.4 Efficient Remyelination: The Role of Cell Signaling Pathways
145(1)
5 Enhancing Endogenous Stem Cells: Current and Future Therapies
146(5)
5.1 Rejuvenation as an Approach to Enhance Remyelination
147(1)
5.2 The Translational Pathway: From Bench to Bedside
147(2)
5.3 Drug Repurposing for Remyelination
149(1)
5.4 Autoantibodies: The Solution From Within
150(1)
6 Concluding Remarks
151(14)
Acknowledgments
154(1)
References
154(11)
Chapter 7 Progenitor cell-based treatment of glial disease
165(26)
Steven A. Goldman
1 Introduction
165(1)
2 GPCs In Vivo
166(1)
3 Identifying Optimal Donor Cell Phenotypes for Treating Myelin Disorders
167(3)
4 Pediatric Myelin Disorders as Targets of Progenitor Cell-Based Therapy
170(4)
4.1 Metabolic and Storage Disorders of Myelin
170(2)
4.2 Disorders of Myelin Formation and Maintenance
172(2)
4.3 The Dilemma of Disease-Specific Dosing
174(1)
5 Adult Disease Targets of GPC-based Treatment
174(3)
5.1 Progenitor Cell Therapy for Multiple Sclerosis
175(1)
5.2 Progenitor Cell Therapy for Adult Structural Demyelinations
175(1)
5.3 Remyelination of Spinal Lesions
176(1)
6 Human Glial Chimeric Mice Reveal Human-Selective Aspects of Both Glial Function and Dysfunction
177(1)
7 Glial Transplant-Mediated Amelioration of Neurodegenerative Disorders
178(3)
8 Human Glial Involvement in---and Potential Rescue of---the Neuropsychiatric Disorders
181(1)
9 Conclusions
182(9)
Acknowledgments
182(1)
References
183(8)
Chapter 8 Pluripotent stem cells and their utility in treating photoreceptor degenerations
191(34)
Nozie D. Aghaizu
Kamil Kruczek
Anai Gonzalez-Cordero
Robin R. Ali
Rachael A. Pearson
1 Introduction
191(1)
2 Retinal Degeneration
192(2)
3 Therapeutic Avenues for Retinal Diseases
194(7)
3.1 Immunotherapy
194(1)
3.2 Gene Therapy
194(1)
3.3 Electronic Retinal Prosthesis
195(1)
3.4 Repair by Cell Transplantation
195(6)
4 Pluripotent Stem Cells
201(6)
4.1 Pioneering Work in Neural Specification and Retinal Differentiation
201(4)
4.2 Growing Retinal Organoids Derived From PSCs
205(2)
5 Challenges for PSC Research
207(2)
6 Clinical Prospects
209(3)
6.1 Cell Transplantation
210(1)
6.2 Disease Modeling
211(1)
6.3 Drug Screening/Evaluation of Potential Treatments
211(1)
7 Conclusion
212(13)
Acknowledgments
212(1)
References
213(12)
Chapter 9 Stem cell-derived retinal pigment epithelium transplantation for treatment of retinal disease
225(20)
Britta Nommiste
Kate Fynes
Victoria E. Tovell
Conor Ramsden
Lyndon da Cruz
Peter Coffey
1 Age-Related Macular Degeneration
226(1)
2 RPE, Its Functions, and Role in AMD
226(3)
3 Proof-of-Principle Studies
229(2)
4 Clinical Results and Considerations
231(3)
5 Production of Cell Therapies for AMD
234(6)
5.1 Regulations
234(1)
5.2 Preclinical Considerations
235(1)
5.3 Manufacturing
236(4)
6 Future
240(5)
Acknowledgments
240(1)
References
241(4)
Chapter 10 Transplantation of reprogrammed neurons for improved recovery after stroke
245(20)
Zaal Kokaia
Daniel Tornero
Olle Lindvall
1 Introduction
245(2)
2 Improving Functional Recovery in Stroke by Transplantation of Reprogrammed Neurons
247(7)
3 Evidence for Reconstruction of Neuronal Circuitry After Implantation of Reprogrammed Cells in Stroke-Injured Brain
254(1)
4 Direct in vitro and in vivo Reprogramming of Somatic Cells to Neurons
255(1)
5 Research Challenges and Prospects for Clinical Translation
256(2)
6 Conclusions
258(7)
Acknowledgments
258(1)
References
259(6)
Combined Index 265
Dunnett is a behavioural neuroscientist who started a lifelong collaboration with the Björklund team in 1979 to explore the functional consequences of cell transplantation method in animal models of neurodegenerative disease, in particular involving cell replacement and repair of the basal ganglia. He has developed models and novel methods of motor and cognitive assessment to apply behavioural analysis not simply to assess functional efficacy of implanted cells, but as a tool to study the mechanisms of cell integration, circuit reconstruction and functional repair. In parallel his laboratory originated the first UK trial of cell transplantation in Huntingtons disease, and provides the source of clinical grade cells for further ongoing trials in Parkinsons disease. Anders Björklund is Senior Professor of neuroscience at Lund University (Sweden). His research career at Lund University spans over more than 50 years, and has resulted in a publication list that covers over 600 papers. His major achievements are in the field of cell transplantation and brain repair. He started this line of research in the mid 1970ies, based on the idea that immature neurons can be used to restore brain circuitry and promote functional recovery in animal models of neurodegenerative diseases. During this period, 1975-1985, his group pioneered this approach using cells obtained from the fetal brain. Anders and his clinical collaborators obtained permission to use tissue from aborted human fetuses in a series of open-label clinical trials in PD patients. Although the outcome of these trials has been quite variable, they have given proof-of-principle that immature dopamin neurons can survive and mature in the striatum in advanced PD patients, and restore dopamine neurotransmission in the area of the striatum re-innervated by the grafted neurons. Since the 1980ies the Lund neural transplantation program has been a leader in the development of restorative therapies in Parkinson´s disease. Current efforts at the Wallenberg Neuroscience center are focused on the development of stem cell-derived dopamine neurons for transplantation, aimed at the development of transplantable neurons derived from human pluripotent stem cells for clinical application. In a parallel line of work Anders group has explored the use of viral vector-mediated gene transfer for neuroprotection and brain repair, with the aim to develop new therapeutic approaches for Parkinson´s disease and other neurodegenerative disorders. In addition, he has pioneered the use of AAV vectors for overexpression of human -synuclein for induction of Parkinson-like neurodegeneration in the nigrostriatal system. This approach has provided a new tool for modeling of the progressive synuclein-induced disease process in animal models of PD.