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Ministerio de Universidades - Gobierno de España

Título: NEUROPROTECTIVE AND IMMUNOMODULATORY ROLES OF ANTI-INFLAMMATORY NEUROPEPTIDES ON CENTRAL NERVOUS SYSTEM DISORDERS
Autor: PEDREÑO MOLINA, MARTA
Universidad: Universidad de Granada
Departamento: Bioquímica y biología molecular III e inmunología
Fecha de Lectura: 09/10/2015
Mención Europeo / Mención Internacional: Concedido
Programa de doctorado: Biomedicina
Dirección:
- DELGADO MORA, MARIO (CODIRECTOR)
- MORELL HITA, MARÍA (CODIRECTOR)
- GONZÁLEZ REY, ELENA (CODIRECTOR)
Tribunal:
- DE LECEA, LUIS (PRESIDENTE)
- Molina Pineda de las Infantas, Ignacio (SECRETARIO)
- Navarro Hilfiker, Sabine Nicole (VOCAL)
- MARTÍN MOLINA, FRANCISCO (VOCAL)
- ROODVELDT CATELLANI, CINTIA (VOCAL)
Descriptores:
- INMUNOLOGIA
- NEUROCIENCIAS
- MICROSCOPIA OPTICA
Localización: DEPARTAMENTO DE BIOQUÍMICA Y BIOLOGÍA MOLECULAR III E INMUNOLOGIA UNIVERSIDAD DE GRANADA
ISBN: 9788491252917

http://0-hera.ugr.es.adrastea.ugr.es/tesisugr/25473605.pdf

Marcador: https://www.educacion.gob.es/teseo/mostrarRef.do?ref=1183284Añadir a favoritos.
Resumen:
Nervous system disorders affect to more than one billion people worldwide and constitute around 35% of the total pool of all diseases in Europe. Due to their high severity and incidence, Multiple Sclerosis (MS) and Parkinson¿s disease (PD) are two important diseases of central nervous system (CNS). MS is a neurodegenerative and autoimmune disease characterized by a chronic inflammatory demyelination and axonal damage of the CNS, being the main cause of non-traumatic disability in young adults. MS pathology is mediated by a Th1/Th17 autoreactive response against the myelin sheath. On the other hand, PD is the second most common neurodegenerative disorder in adults over the age of 65. It is characterized by a progressive degeneration of dopaminergic neurons of the substantia nigra pars compacta (SNpc) and their projections to the striatum. In the last years it has been accepted that the immune system also has a role in PD, where neuroinflammation seems to be a hallmark of its pathogenesis. Due to their complex pathophysiology, there is no effective cure for both disorders, being necessary looking for new treatments that act through a multitarget approach. In the last years, our lab has identified several neuropeptidesthat show anti-inflammatory and immunomodulatory profiles. Among them, adrenomedullin and cortistatin seem also to have neuroprotective roles. The aim of the present study is to investigate the role of both neuropeptides in diseases of the CNS characterized by a disrupted immune response leading to neuroinflammation and neurodegeneration. We used a well-established pre-clinic model of MS, the experimental autoimmune encephalomyelitis (EAE) to assay the therapeutic potential of adrenomedullin. We demonstrated that adrenomedullin is able to reduce the incidence and severity of the disease, even when the disease was fully established. Moreover, the treatment of mice suffering EAE with adrenomedullin reduced the inflammatory infiltration, the number of demyelinating plaques, and the production of pro-inflammatory mediators in spinal cord and/or brain. Furthermore, adrenomedullin was able to modulate the Th1/Th17 autoreactive response in the lymphoid organs and in the CNS. Interestingly, this effect was specific of the encephalitogenic antigent, and it seems to be related with the fact that the treatment with adrenomedullin generated immune tolerance by inducing regulatory T (Treg) cells and tolerogenic dendritic cells that were able to control the progression of the disease. Additionally, adrenomedullin promoted neuroprotective responses by up-regulating the expression of neurotrophic factors. Accordingly, using a focal model of demyelination induced by the injection of the toxin lysolecithin, we demonstrated that adrenomedullindecreased the demyelinating area and increased the number of oligodendrocytes, suggesting a role on remyelination. Otherwise, adrenomedullin inactivates resident cells of CNS in presence of pro-inflammatory stimulus. On the other hand, we previously described the beneficial effect of cortistatin in EAE. Therefore, we decided to analyze the potential therapeutic effect of this neuropeptide in a preclinical mouse model of PD induced by acute exposure to the neurotoxin MPTP. We observed that treatment with cortistatin reduced the loss of dopaminergic neurons in the SNpc and their projections to the striatum caused by MPTP injection. This effect correlated with an improvement in the locomotor activity. Furthermore, in an in vitro model of PD, cortistatin decreased cell death of dopaminergic neurons caused by MPP+. Moreover, cortistatin diminished the presence and activation of microglia cells and astrocytes in the SNpc of MPTP-mice, suggesting a role of this neuropeptide in the regulation of neuroinflammation associated to this disorder. Furthermore, cortistatin induced the expression of neurotrophic factors. We also observed that cortistatin modulated the immune response of glial cells in the presence of ¿-synuclein, as extracellular stimuli. Finally, animals deficient in cortistatin also revealed the relevance of this neuropeptide in the development and progression of this neurodegenerative disorder. Together, our results suggest that adrenomedullin and cortistatin emerge as potential new therapeutic agents that combine their anti-inflammatory, immunomodulatory and neuroprotective properties to regulate at multiple levels the progression of CNS disorders.

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