Comparison of the Neural Differentiation Potential of Human Mesenchymal Stem Cells from Amniotic Fluid and Adult Bone Marrow
Autor: | Hong-tian Zhang, Yu-Qin Hu, Ruxiang Xu, Zhong-jie Yan, Peng Zhang, Changchen Hu, Xinlin Sun, Zongyu Xiao, Ying-qian Cai |
---|---|
Rok vydání: | 2013 |
Předmět: |
Adult
Pathology medicine.medical_specialty Neurogenesis Clinical uses of mesenchymal stem cells Bone Marrow Cells Cell Separation Biology Immunophenotyping Mice Young Adult Cellular and Molecular Neuroscience Neural Stem Cells Chromosomal Instability Neurosphere medicine Animals Humans Nerve Growth Factors Cell Shape Cell Proliferation Stem cell transplantation for articular cartilage repair Neurons Multipotent Stem Cells Mesenchymal stem cell Mesenchymal Stem Cells Amniotic stem cells Cell Biology General Medicine Middle Aged Amniotic Fluid Chromosomes Mammalian Cell biology Cell Transformation Neoplastic Karyotyping Amniotic epithelial cells Stem cell Biomarkers Adult stem cell |
Zdroj: | Cellular and Molecular Neurobiology. 33:465-475 |
ISSN: | 1573-6830 0272-4340 |
DOI: | 10.1007/s10571-013-9922-y |
Popis: | Human mesenchymal stem cells (MSCs) are considered a promising tool for cell-based therapies of nervous system diseases. Bone marrow (BM) has been the traditional source of MSCs (BM-MSCs). However, there are some limitations for their clinical use, such as the decline in cell number and differentiation potential with age. Recently, amniotic fluid (AF)-derived MSCs (AF-MSCs) have been shown to express embryonic and adult stem cell markers, and can differentiate into cells of all three germ layers. In this study, we isolated AF-MSCs from second-trimester AF by limiting dilution and compared their proliferative capacity, multipotency, neural differentiation ability, and secretion of neurotrophins to those of BM-MSCs. AF-MSCs showed a higher proliferative capacity and more rapidly formed and expanded neurospheres compared to those of BM-MSCs. Both immunocytochemical and quantitative real-time PCR analyses demonstrated that AF-MSCs showed higher expression of neural stemness markers than those of BM-MSCs following neural stem cell (NSC) differentiation. Furthermore, the levels of brain-derived growth factor and nerve growth factor secreted by AF-MSCs in the culture medium were higher than those of BM-MSCs. In addition, AF-MSCs maintained a normal karyotype in long-term cultures after NSC differentiation and were not tumorigenic in vivo. Our findings suggest that AF-MSCs are a promising and safe alternative to BM-MSCs for therapy of nervous system diseases. |
Databáze: | OpenAIRE |
Externí odkaz: |