Ysis tools. Nucleic Acids Res 1997, 25:4876-4882. 65. Bininda-Emonds O…

Ysis tools. Nucleic Acids Res 1997, 25:4876-4882. 65. Bininda-Emonds OR: transAlign: using amino acids to facilitate the multiple alignment of protein-coding DNA sequences. BMC Bioinformatics 2005, 6:156. 66. Yang Z, Nielsen R: Estimating synonymous and nonsynonymous substitution rates under realistic evolutionary models. Mol Biol Evol 2000, 17:32-43. 67. Yang Z: PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol 2007, 24:1586-1591.doi: 10.1186/1471-2164-11-258 Cite this article as: Roxstr -Lindquist et al., Large genomic differences between the morphologically indistinguishable diplomonads Spironucleus barkhanus and Spironucleus salmonicida BMC Genomics 2010, 11:
Amemori et al. Stem Cell Research Therapy 2013, 4:68 http://stemcellres.com/content/4/3/RESEARCHOpen AccessHuman conditionally immortalized neural stem cells improve locomotor function after spinal cord injury in the ratTakashi Amemori1, Nataliya Romanyuk1, Pavla Jendelova1,2*, Vit Herynek3, Karolina Turnovcova1, Pavel Prochazka1, Miroslava Kapcalova1, Graham Cocks4, Jack Price4 and Eva Sykova1,AbstractIntroduction: A growing number of studies have highlighted the potential of stem cell and more-differentiated neural cell transplantation as intriguing therapeutic approaches for neural repair after spinal cord injury (SCI). Methods: A conditionally PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/6388955 immortalized neural stem cell line derived from human fetal spinal cord tissue (SPC-01) was used to treat a balloon-induced SCI. SPC-01 cells were implanted into the lesion 1 week after SCI. To determine the feasibility of tracking transplanted stem cells, a portion of the SPC-01 cells was labeled with poly-L-lysine-coated superparamagnetic iron-oxide nanoparticles, and the animals grafted with labeled cells underwent magnetic resonance imaging. Functional recovery was evaluated by using the BBB and plantar tests, and lesion morphology, endogenous axonal sprouting and graft survival, and differentiation were analyzed. Quantitative polymerase chain reaction (qPCR) was used to evaluate the effect of transplanted SPC-01 cells on endogenous regenerative processes. Results: Transplanted animals displayed significant motor and sensory improvement 2 months after SCI, when the cells robustly survived in the lesion and partially filled the lesion cavity. qPCR revealed the increased expression of rat and human neurotrophin and motor neuron genes. The grafted cells were immunohistologically positive for glial fibrillary acidic protein (GFAP); however, we found 25 of the cells to be positive for Nkx6.1, an Capivasertib early motor neuron marker. Spared white matter and the robust sprouting of growth-associated protein 43 (GAP43)+ axons were found in the host tissue. Four months after SCI, the grafted cells matured into Islet2+ and choline acetyltransferase (ChAT)+ neurons, and the graft was grown through with endogenous neurons. Grafted cells labeled with poly-L-lysine-coated superparamagnetic nanoparticles before transplantation were detected in the lesion on T2-weighted images as hypointense spots that correlated with histologic staining for iron and the human mitochondrial marker MTCO2. Conclusions: The transplantation of SPC-01 cells produced significant early functional improvement after SCI, suggesting an early neurotrophic action associated with long-term restoration of the host tissue, making the cells a promising candidate for future cell therapy in patients with SCI. Keywords: Human fetal neural stem cells, spinal cord injury, mot.