Mouse Neural Stem Cell Differentiation and Human Adipose Mesenchymal Stem Cell Transdifferentiation Into Neuron- and Oligodendrocyte-like Cells With Myelination Potential

• Published in: Stem cell reviews and reports Vol. 18; no. 2; pp. 732 - 751
• Main Authors: Santos, Anderson K., Gomes, Katia N., Parreira, Ricardo C., Scalzo, Sérgio, Pinto, Mauro C. X., Santiago, Helton C., Birbrair, Alexander, Sack, Ulrich, Ulrich, Henning, Resende, Rodrigo R.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.02.2022; Springer Nature B.V
• Subjects: Angiogenesis; Animals; Astrocytes; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Cell Biology; Cell Differentiation; Cell proliferation; Cell therapy; Cell Transdifferentiation; Cells, Cultured; Excitability; Gene expression; Glial fibrillary acidic protein; Humans; Life Sciences; Mesenchymal stem cells; Mice; Microtubule-associated protein 2; Myelination; Nestin; Neural plasticity; Neural Stem Cells; Neurogenesis; Neuronal-glial interactions; Neurons; Oligodendrocytes; Oligodendroglia; Phenotypes; Platelet-derived growth factor; Regeneration; Regenerative Medicine/Tissue Engineering; Special issue on Neurogenesis and Neurodegeneration: Basic Research and Clinic Applications; Stem cell transplantation; Stem Cells; Synaptic plasticity; Tubulin; Neural stem cells; Myelination; Adult stem cells; Neural differentiation; Transdifferentiation
• ISSN: 2629-3269; 2629-3277
• DOI: 10.1007/s12015-021-10218-7

Stem cell therapy is an interesting approach for neural repair, once it can improve and increase processes, like angiogenesis, neurogenesis, and synaptic plasticity. In this regard, adult neural stem cells (NSC) are studied for their mechanisms of proliferation, differentiation and functionality in neural repair. Here, we describe novel neural differentiation methods. NSC from adult mouse brains and human adipose-derived stem cells (hADSC) were isolated and characterized regarding their neural differentiation potential based on neural marker expression profiles. For both cell types, their capabilities of differentiating into neuron-, astrocyte- and oligodendrocytes-like cells (NLC, ALC and OLC, respectively) were analyzed. Our methodologies were capable of producing NLC, ALC and OLC from adult murine and human transdifferentiated NSC. NSC showed augmented gene expression of NES, TUJ1, GFAP and PDGFRA/Cnp . Following differentiation induction into NLC, OLC or ALC, specific neural phenotypes were obtained expressing MAP2, GalC/O4 or GFAP with compatible morphologies, respectively. Accordingly, immunostaining for nestin + in NSC, GFAP + in astrocytes and GalC/O4 + in oligodendrocytes was detected. Co-cultured NLC and OLC showed excitability in 81.3% of cells and 23.5% of neuron/oligodendrocyte marker expression overlap indicating occurrence of in vitro myelination. We show here that hADSC can be transdifferentiated into NSC and distinct neural phenotypes with the occurrence of neuron myelination in vitro, providing novel strategies for CNS regeneration therapy. Graphical Abstract Superior Part : Schematic organization of obtaining and generating hNSC from hADSC and differentiation processes and phenotypic expression of neuron, astrocyte and oligodendrocyte markers (MAP2, GFAP and O4, respectively) and stem cell marker (NES) of differentiating hNSC 14 days after induction. The nuclear staining in blue corresponds to DAPI. bar = 100 μm. Inferior part: Neural phenotype fates in diverse differentiation media. NES: nestin; GFAP: Glial fibrillary acidic protein. MAP2: Microtubule-associated protein 2. TUJ1: β-III tubulin. PDGFRA: PDGF receptor alpha. Two-way ANOVA with Bonferroni post-test with n  = 3. * p  < 0.05 and ** p  < 0.01: (NSCiM1 NSC induction medium 1) vs differentiation media.