Promoting motor functions in a spinal cord injury model of rats using transplantation of differentiated human olfactory stem cells: A step towards future therapy

• Published in: Behavioural brain research 2021-05, Vol.405, p.113205-113205, Article 113205
• Main Authors: Hamidabadi, Hatef Ghasemi, Simorgh, Sara, Kamrava, Seyed Kamran, Namjoo, Zeinab, Bagher, Zohreh, Bojnordi, Maryam Nazm, Niapour, Ali, Mojaverrostami, Sina, Saeb, Mohammad Reza, Zarrintaj, Payam, Olya, Arta, Alizadeh, Rafieh
• Format: Article
• Language: English
• Subjects: Animals; Behavior, Animal - physiology; Cells, Cultured; Disease Models, Animal; Engraftment; Human olfactory ecto-mesenchymal stem cells (hOE-MSCs); Humans; Locomotion - physiology; Male; Mesenchymal Stem Cell Transplantation; motor neuron; Motor Neurons - physiology; Olfactory Mucosa - cytology; Rats; Rats, Sprague-Dawley; Spinal Cord Injuries - therapy; Spinal cord injury; Stem cells
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2021.113205

•Human olfactory stem cells could differentiate into motor neurons.•Human olfactory stem cells could promote motor function in a spinal cord injury rat mode.•Motor neurons derived olfactory stem cells gives better results in promotion of motor function. Human olfactory ecto-mesenchymal stem cells (hOE-MSCs) derived from the human olfactory mucosa (OM) can be easily isolated and expanded in cultures while their immense plasticity is maintained. To mitigate ethical concerns, the hOE-MSCs can be also transplanted across allogeneic barriers, making them desirable cells for clinical applications. The main purpose of this study was to evaluate the effects of administering the hOE-MSCs on a spinal cord injury (SCI) model of rats. These cells were accordingly isolated and cultured, and then treated in the neurobasal medium containing serum-free Dulbecco’s Modified Essential Medium (DMEM) and Ham’s F-12 Medium (DMEM/F12) with 2% B27 for two days. Afterwards, the pre-induced cells were incubated in N2B27 with basic fibroblast growth factor (bFGF), fibroblast growth factor 8b (FGF8b), sonic hedgehog (SHH), and ascorbic acid (vitamin C) for six days. The efficacy of the induced cells was additionally evaluated using immunocytochemistry (ICC) and real-time polymerase chain reaction (RT-PCR). The differentiated cells were similarly transplanted into the SC contusions. Functional recovery was further conducted on a weekly basis for eight consecutive weeks. Moreover, cell integration was assessed via conventional histology and ICC, whose results revealed the expression of choline acetyltransferase (ChAT) marker at the induction stage. According to the RT-PCR findings, the highest expression level of insulin gene-enhancer protein (islet-1), oligodendrocyte transcription factor (Olig2), and homeobox protein HB9 was observed at the induction stage. The number of engraftment cells also rose (approximately by 2.5 % ± 0.1) in the motor neuron-like cells derived from the hOE-MSCs-grafted group compared with the OE-MSCs-grafted one. The functional analysis correspondingly revealed that locomotor and sensory scores considerably improved in the rats in the treatment group. These findings suggested that motor neuron-like cells derived from the hOE-MSCs could be utilized as an alternative cell-based therapeutic strategy for SCI.