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Olfactory mucosa stem cells: An available candidate for the treatment of the Parkinson's disease
Author(s) -
Simorgh Sara,
Alizadeh Rafieh,
Eftekharzadeh Mina,
Haramshahi Seyed Mohammad Amin,
Milan Peiman Brouki,
Doshmanziari Maryam,
Ramezanpour Farnaz,
Gholipourmalekabadi Mazaher,
Seifi Morteza,
Moradi Fatemeh
Publication year - 2019
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.28944
Subject(s) - olfactory mucosa , substantia nigra , transplantation , tyrosine hydroxylase , parkinson's disease , pars compacta , mesenchymal stem cell , pathology , dopaminergic , dopamine , biology , medicine , immunohistochemistry , neuroscience , disease , olfactory system
Olfactory ectomesenchymal stem cells (OE‐MSCs) possess the immunosuppressive activity and regeneration capacity and hold a lot of promises for neurodegenerative disorders treatment. This study aimed to determine OE‐MSCs which are able to augment and differentiate into functional neurons and regenerate the CNS and also examine whether the implantation of OE‐MSCs in the pars compacta of the substantia nigra (SNpc) can improve Parkinson's symptoms in a rat model‐induced with 6‐hydroxydopamine. We isolated OE‐MSCs from lamina propria in olfactory mucosa and characterized them using flow cytometry and immunocytochemistry. The therapeutic potential of OE‐MSCs was evaluated by the transplantation of isolated cells using a rat model of acute SN injury as a Parkinson's disease. Significant behavioral improvement in Parkinsonian rats was elicited by the OE‐MSCs. The results demonstrate that the expression of PAX2, PAX5, PITX3, dopamine transporter, and tyrosine hydroxylase was increased by OE‐MSCs compared to the control group which is analyzed with real‐time polymerase chain reaction technique and immunohistochemical staining. In the outcome, the transplantation of 1,1′‐dioctadecyl‐3,3,3′3'‐tetramethyl indocarbocyanine perchlorate labeled OE‐MSCs that were fully differentiated to dopaminergic neurons contribute to a substantial improvement in patients with Parkinson's. Together, our results provide that using OE‐MSCs in neurodegenerative disorders might lead to better neural regeneration.