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Vol. 2. Núm. S1.
Biomaterial and stem cell -based treatment strategies for diseases of the central nervous system
Páginas S1-S2 (enero 2021)
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Vol. 2. Núm. S1.
Biomaterial and stem cell -based treatment strategies for diseases of the central nervous system
Páginas S1-S2 (enero 2021)
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Biomaterial- and stem cell–based treatment strategies for diseases of the central nervous system
Estrategias terapéuticas basadas en biomateriales y células madre en patologías del sistema nervioso central
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A. Canales-Aguirreb, J.C. Mateos-Díazc, J. Matias-Guiud, U. Gomez-Pinedoa,
Autor para correspondencia
u.gomez.pinedo@gmail.com

Corresponding author.
a Department of Neurology, Laboratory of Neurobiology, Institute of Neurosciences, San Carlos Health Research Institute, Universidad Complutense, Spain
b Preclinical Evaluation Unit, Medical and Pharmaceutical Biotechnology Unit. CIATEJ-CONACyT, Guadalajara, Mexico
c Department of Industrial Biotechnology, CIATEJ-CONACyT, Guadalajara, Mexico
d Department of Neurology, Institute of Neurosciences, San Carlos Health Research Institute, Universidad Complutense, Madrid, Spain
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Vol. 2. Núm S1

Biomaterial and stem cell -based treatment strategies for diseases of the central nervous system

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The research topic “Biomaterial- and stem cell– based treatment strategies for diseases of the central nervous system,” including 7 articles, seeks to underscore the importance of translational research in the area of cell therapy and tissue engineering.

Today, the generation of novel treatment strategies for diseases of the central nervous system, such as vascular (stroke, hypoxia), oncological (gliomas), infectious, or neurodegenerative diseases (Parkinson's disease, amyotrophic lateral sclerosis, etc.), has created new areas of research involving close collaboration between the fields of basic and clinical research.

The path forward is promising, and bioengineering is evolving day by day, with the development of new materials biocompatible with nervous tissue, enabling the design of in vitro systems to study pathophysiological mechanisms in tumoural or infectious diseases of the nervous system. As well as serving as a platform for the development of personalised in vitro models of complex diseases, these models also help elucidate their structural formation and cell-biomaterial integration, as a basis for the future development of biomaterials preloaded with pluripotent stem cells or as vehicles for drugs and bioactive compounds. The development of these constructs aims to promote endogenous restoration of neural tissue lesions and to promote axonal connection.1–4

Alongside the development of tissue engineering, cell therapy has evolved over the last 3 decades, seeking new ways to restore or promote regeneration, cell plasticity, or the action of implanted cells as small trophic pumps in such lesions as stroke, hypoxia, spinal injury, and gliomas. One of the most successful strategies, as evidenced by the number of clinical and preclinical trials, is the use of mesenchymal stem cells, which have shown benefits and therapeutic potential in diseases involving inflammatory mechanisms, such as stroke and neonatal hypoxia.5

In the context of neurodegenerative disease, such as Parkinson's disease, several study groups have explored the potential of a range of cell types to increase the number of dopaminergic neurons and to promote their projections to the striatum, or as trophic pumps to increase baseline dopamine levels, as has already been demonstrated with the implantation of cells from the carotid body. Furthermore, several preclinical trials have used biomaterial bridges preloaded with glial or stem cells to promote or orient axonal projections from the substantia nigra to the striatum, with promising results.6

Finally, cell therapy with mesenchymal stem cells is a promising strategy in amyotrophic lateral sclerosis, and has been demonstrated to modulate inflammation and delay the onset of symptoms of the disease.7

We are confident that the path forward in this area of biomedical research may generate more projects and greater interest in the scientific community through synergy between different disciplines, benefiting the population in the short term.

References
[1.]
R. Ramos-Zúñiga, I. Segura-Duran, R.E. González-Castañeda, J.A. González-Rios.
The challenges of the bioactive scaffolds in nervous system: From their molecular conformation to their therapeutic efficiency.
Neurology Perspectives, (2021),
[2.]
Y.K. Gutiérrez-Mercadoa, J.C. Mateos-Díaz, D.D. Ojeda-Hernándezb, F.J. López-Gonzalez, E.E. Reza-Zaldivard, M.A. Hernández-Sapiens, U.A. Gómez-Pinedo, R.S. Estrada, M. Macías-Carballo, A.A. Canales-Aguirre.
Ortho-coumaric acid derivatives with therapeutic potential in a three-dimensional culture of the immortalised U-138 MG glioblastoma multiforme cell line.
Neurology Perspectives, (2021),
[3.]
J.R. Aguilera-Márquez, G. Tonantzin de Dios Figueroa, E.E. Reza-Saldivar, T.A. Camacho-Villegas, A.A. Canales-Aguirre, P. Hayl-Fabres.
Biomaterials: Emerging systems for study and treatment of Glioblastoma Multiforme.
Neurology Perspectives, (2021),
[4.]
F.J. Galvez-Gastelum, I. Yañez-Sánchez, B.C. Zamarripa-Pérez.
Nanomaterials application in Neisseria meningitidis infections.
Neurology Perspectives, (2021),
[5.]
A. del Pozo, M. Villa, J. Martínez-Orgado.
Potential therapeutic applications of stem cell therapy for neonatal hypoxic-ischaemic brain injury.
Neurology Perspectives, (2021),
[6.]
F.J. Sancho-Bielsa.
Parkinson's disease: Present and future of cell therapy.
Neurology Perspectives, (2021),
[7.]
Cell therapy as therapeutic strategy in Amyotrophic Lateral Sclerosis. Gomez-Pinedo, L. Moreno-Jiménez, M.S. Benito-Martín, A. Abad-Fernández, B. Selma-Calvo, N. Fernandez-Cucho, J. A. Matias-Guiu, L. Galán-Dávila, A. Guerrero-Sola, J. Matías-Guiu.
Copyright © 2021. Sociedad Española de Neurología
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