Evaluation of Motor Neuron-Like Cell Differentiation of hEnSCs on Biodegradable PLGA Nanofiber Scaffolds

• Published in: Molecular neurobiology Vol. 52; no. 3; pp. 1704 - 1713
• Main Authors: Ebrahimi-Barough, Somayeh, Norouzi Javidan, Abbas, Saberi, Hoshangh, Joghataei, Mohammad Tghi, Rahbarghazi, Reza, Mirzaei, Esmaeil, Faghihi, Faezeh, Shirian, Sadegh, Ai, Armin, Ai, Jafar
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-12-2015; Springer Nature B.V
• Subjects: Absorbable Implants; Biochemistry; Biodegradation; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cell Differentiation - drug effects; Cell Lineage - drug effects; Cell Lineage - physiology; Cell Proliferation - drug effects; Cell Survival - drug effects; Cells, Cultured; Humans; Lactic Acid - pharmacology; Motor ability; Motor Neurons - cytology; Nanofibers; Nervous system; Neurobiology; Neurology; Neurons; Neurosciences; Polyglycolic Acid - pharmacology; Regeneration - drug effects; Stem cells; Stem Cells - cytology; Tissues; Motor neuron differentiation; Nanofibrous scaffolds; PLGA; Human endometrial stem cell
• ISSN: 0893-7648; 1559-1182
• DOI: 10.1007/s12035-014-8931-2

Human endometrium is a high-dynamic tissue that contains human endometrial stem cells (hEnSCs) which can be differentiated into a number of cell lineages. The differentiation of hEnSCs into many cell lineages such as osteoblast, adipocyte, and neural cells has been investigated previously. However, the differentiation of these stem cells into motor neuron-like cells has not been investigated yet. Different biochemical and topographical cues can affect the differentiation of stem cells into a specific cell. The aim of this study was to investigate the capability of hEnSCs to be differentiated into motor neuron-like cells under biochemical and topographical cues. The biocompatible and biodegradable poly(lactic-co-glycolic acid) (PLGA) electrospun nanofibrous scaffold was used as a topographical cue. Human EnSCs were cultured on the PLGA scaffold and tissue culture polystyrene (TCP), then differentiation of hEnSCs into motor neuron-like cells under induction media including retinoic acid (RA) and sonic hedgehog (Shh) were evaluated for 15 days. The proliferation rate of cells was assayed by using MTT assay. The morphology of cells was studied by scanning electron microscopy imaging, and the expression of motor neuron-specific markers by real-time PCR and immunocytochemistry. Results showed that survival and differentiation of hEnSCs into motor neuron-like cells on the PLGA scaffold were better than those on the TCP group. Taken together, the results suggest that differentiated hEnSCs on PLGA can provide a suitable, three-dimensional situation for neuronal survival and outgrowth for regeneration of the central nervous system, and these cells may be a potential candidate in cellular therapy for motor neuron diseases.