Direct Conversion of Human Fibroblasts to Induced Neurons

Author(s):  
Lucia Zhou-Yang ◽  
Sophie Eichhorner ◽  
Lukas Karbacher ◽  
Lena Böhnke ◽  
Larissa Traxler ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Natalia Avaliani ◽  
Ulrich Pfisterer ◽  
Andreas Heuer ◽  
Malin Parmar ◽  
Merab Kokaia ◽  
...  

Direct conversion of human somatic cells to induced neurons (iNs), using lineage-specific transcription factors has opened new opportunities for cell therapy in a number of neurological diseases, including epilepsy. In most severe cases of epilepsy, seizures often originate in the hippocampus, where populations of inhibitory interneurons degenerate. Thus, iNs could be of potential use to replace these lost interneurons. It is not known, however, if iNs survive and maintain functional neuronal properties for prolonged time periods in in vivo. We transplanted human fibroblast-derived iNs into the adult rat hippocampus and observed a progressive morphological differentiation, with more developed dendritic arborisation at six months as compared to one month. This was accompanied by mature electrophysiological properties and fast high amplitude action potentials at six months after transplantation. This proof-of-principle study suggests that human iNs can be developed as a candidate source for cell replacement therapy in temporal lobe epilepsy.


Nature ◽  
2010 ◽  
Vol 468 (7323) ◽  
pp. 521-526 ◽  
Author(s):  
Eva Szabo ◽  
Shravanti Rampalli ◽  
Ruth M. Risueño ◽  
Angelique Schnerch ◽  
Ryan Mitchell ◽  
...  

2019 ◽  
Vol 10 (9) ◽  
Author(s):  
Xiu Sun ◽  
Zijian Tan ◽  
Xiao Huang ◽  
Xueyan Cheng ◽  
Yimin Yuan ◽  
...  

Abstract Direct conversion of readily available non-neural cells from patients into induced neurons holds great promise for neurological disease modeling and cell-based therapy. Olfactory ensheathing cells (OECs) is a unique population of glia in olfactory nervous system. Based on the regeneration-promoting properties and the relative clinical accessibility, OECs are attracting increasing attention from neuroscientists as potential therapeutic agents for use in neural repair. Here, we report that OECs can be directly, rapidly and efficiently reprogrammed into neuronal cells by the single transcription factor Neurogenin 2 (NGN2). These induced cells exhibit typical neuronal morphologies, express multiple neuron-specific markers, produce action potentials, and form functional synapses. Genome-wide RNA-sequencing analysis shows that the transcriptome profile of OECs is effectively reprogrammed towards that of neuronal lineage. Importantly, these OEC-derived induced neurons survive and mature after transplantation into adult mouse spinal cords. Taken together, our study provides a direct and efficient strategy to quickly obtain neuronal cells from adult OECs, suggestive of promising potential for personalized disease modeling and cell replacement-mediated therapeutic approaches to neurological disorders.


2020 ◽  
Vol 48 ◽  
pp. 101984 ◽  
Author(s):  
Mette Habekost ◽  
Arne Lund Jørgensen ◽  
Per Qvist ◽  
Mark Denham

2019 ◽  
Author(s):  
Itaru Ninomiya ◽  
Masato Kanazawa ◽  
Akihide Koyama ◽  
Masahiro Hatakeyama ◽  
Osamu Onodera

SummaryPrevious studies reported that human fibroblasts and astrocytes were successfully converted into neuronal cells by small molecules without introducing ectopic transgenes. Induced neuronal cells—reprogrammed directly from dermal fibroblasts or brain astrocytes—were obtained from some donors; however, the clinical applications of this approach would be limited because it requires an invasive biopsy to harvest enough cells for derivation. Here, we report that adult human peripheral blood monocytes may be directly converted into neuron-like cells using only a combination of small molecules without transgene integration. This method enables neuronal cell generation from TUJ1-positive cells after 3 days of induction (at over 80% conversion efficacy). These cells presented neuronal morphologies and markers, suggesting that terminally differentiated human cells may be efficiently transdifferentiated into a distantly related lineage. Overall, our study provides a strategy to develop neuronal cells directly from human adult peripheral blood monocytes using a generate transgene-free, chemical-only approach.


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