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Differentiation potential of menstrual blood‐ versus bone marrow‐stem cells into glial‐like cells
Author(s) -
Azedi Fereshteh,
Kazemnejad Somaieh,
Zarnani Amir Hassan,
Behzadi Gila,
Vasei Mohammad,
Khanmohammadi Manijeh,
Khanjani Sayeh,
Edalatkhah Haleh,
Lakpour Niknam
Publication year - 2014
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1002/cbin.10245
Subject(s) - nestin , stem cell , glial fibrillary acidic protein , neurosphere , neural stem cell , microbiology and biotechnology , biology , bone marrow , immunology , stem cell marker , cellular differentiation , chemistry , adult stem cell , immunohistochemistry , biochemistry , gene
Abstract Menstrual blood is easily accessible, renewable, and inexpensive source of stem cells that have been interested for cell therapy of neurodegenerative diseases. In this study, we showed conversion of menstrual blood stem cells (MenSCs) into clonogenic neurosphere‐ like cells (NSCs), which can be differentiated into glial‐like cells. Moreover, differentiation potential of MenSCs into glial lineage was compared with bone marrow stem cells (BMSCs). Differentiation potential of individual converted NSCs derived from MenSCs or BMSCs into glial‐like cells was investigated using immunofluorescence staining and real‐time polymerase chain reaction.The fibroblastic morphology of both MenSCs and BMSCs was turned into NSCs shape during first step of differentiation. NSCs derived from both BMSCs and MenSCs expressed higher levels of Olig‐2 and Nestin markers compared to undifferentiated cells. The expression levels of myelin basic protein (MBP) mRNA up regulated only in BMSCs‐NSCs no in MenSCs‐NSCs. However, outgrowth of individual NSCs derived from both MenSCs and BMSCs into glial‐like cells led to significant up regulation of glial fibrillary acidic protein,Olig‐2 and MBP at mRNA and protein level accompanied with down regulation of Nestin protein.This is the first study demonstrating that MenSCs can be converted to NSCs with differentiation ability into glial‐like cells. Accumulative data show different expression pattern of glial markers in differentiated MenSCs compared to BMSCs. The comparable differentiation potential, more accessibility and no invasive technique for sample collection of MenSCs in comparison with BMSCs introduce MenSCs as an apt, consistent and safe alternative to BMSCs for cell therapy of neurodegenerative diseases.