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<dc:title>Directly induced Neural Stem Cells transplantation and prospects for stem cell-based therapy</dc:title>
<dc:creator>VICARIO, NUNZIO</dc:creator>
<dc:contributor>Vicario, Nunzio</dc:contributor>
<dc:contributor>CARDILE, Venera</dc:contributor>
<dc:contributor>SALOMONE, Salvatore</dc:contributor>
<dc:subject>Stem Cells Transplantation, induced neural stem cells (iNSCs), Demyelination, Remyelination, Multiple Sclerosis.</dc:subject>
<dc:description>Despite the remarkable beneficial effects of disease-modifying agents in relapsing-remitting multiple&#xd;
sclerosis (MS) patients, progressive forms of (P)MS still lack effective treatments. This stark contrast is&#xd;
partially dependent on the difficulties researchers have found in tackling the complex pathophysiology of this&#xd;
phase of disease, in which chronic inflammation within the central nervous system (CNS) is coupled by&#xd;
ongoing neurodegeneration and demyelination.&#xd;
Cell transplantation is among the most promising therapeutic approaches in regenerative medicine,&#xd;
combining tissue trophic and immunomodulatory effects of the graft with its intrinsic potential for cellreplacement.&#xd;
These are all attributes that can be harnessed to treated patients with PMS.&#xd;
As such, within this thesis, I have focused my attention on investigating how cellular therapies could be used&#xd;
to (i) prevent neuronal damage, (ii) modulate the chronic activation of the immune system and (iii) replace&#xd;
the damaged myelin in PMS.&#xd;
Olfactory Ensheathing Cells (OECs) are a special population of glial cells known to exert neuroprotective&#xd;
mechanisms and capable of promoting neuroprotection. Using in vitro models of neuron-like cells, I have&#xd;
demonstrated that OECs exert their neuroprotective effect by reducing Cx43-mediated cell-to-cell and cell-toextracellular&#xd;
environment communications. Despite this important finding, the immunomodulatory and&#xd;
remyelinating potential of OECs is still limited. As such, I decided to study a complementary stem cell&#xd;
approach that conjugates these attributes with ease in clinical applicability.&#xd;
Induced Neural Stem Cells (iNSCs) are a source of autologous, stably expandable, tissue specific and easily&#xd;
accessible stem cells, which have the potential to differentiate into the three main neural lineages. Mouse&#xd;
iNSCs were characterized in vitro and in vivo and their immunomodulatory potential was initially studied. This&#xd;
work uncovered a novel mechanism that underpins the potential of iNSCs to interact with the chronic CNS&#xd;
compartmentalised activation of the innate immune system. Specifically, I found that iNSCs are able to&#xd;
sense extracellular metabolites, which accumulate in the chronically inflamed CNS, and to ameliorate&#xd;
neuroinflammation via succinate-SUCNR1-dependend mechanisms. To characterize the potential for tissue&#xd;
replacement and remyelination of such a promising cell line, I have also analysed how iNSCs grafts&#xd;
differentiate in an experimental model of focal demyelination. I found that iNSCs are able to integrate and&#xd;
differentiate into remyelinating oligodendrocytes (OLs) in chronic demyelinated CNS. These data suggest&#xd;
that iNSCs are indeed an effective source of stem cell transplantation, being able to modulate inflammation&#xd;
and to effectively replace lost tissue in mouse models of PMS.&#xd;
Altogether the evidences gathered in this thesis are important new steps in the field of cell transplantation,&#xd;
which will be pivotal in the march forward for future clinical applications in chronic demyelinating CNS&#xd;
disorders.</dc:description>
<dc:date>2017-11-20</dc:date>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
<dc:identifier>https://hdl.handle.net/20.500.11769/583115</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Università degli studi di Catania</dc:publisher>
<dc:publisher>place:Catania</dc:publisher>
<dc:rights>license:PUBBLICO - Pubblico con Copyright</dc:rights>
<dc:rights>license uri:iris.PUB02</dc:rights>
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