In Vitro Differentiation of Human Skin-Derived Cells into Functional Sensory Neurons-Like.
Adeline BatailleRaphael LeschieraKillian L'HérondelleJean-Pierre PennecNelig Le GouxOlivier MignenMehdi SakkaEmmanuelle Plée-GautierCécilia BrunThierry OddosJean-Luc CarréLaurent MiséryNicolas LebonvalletPublished in: Cells (2020)
Skin-derived precursor cells (SKPs) are neural crest stem cells that persist in certain adult tissues, particularly in the skin. They can generate a large type of cell in vitro, including neurons. SKPs were induced to differentiate into sensory neurons (SNs) by molecules that were previously shown to be important for the generation of SNs: purmorphamine, CHIR99021, BMP4, GDNF, BDNF, and NGF. We showed that the differentiation of SKPs induced the upregulation of neurogenins. At the end of the differentiation protocol, transcriptional analysis was performed on BRN3A and a marker of pain-sensing nerve cell PRDM12 genes: 1000 times higher for PRDM12 and 2500 times higher for BRN3A in differentiated cells than they were in undifferentiated SKPs. Using immunostaining, we showed that 65% and 80% of cells expressed peripheral neuron markers BRN3A and PERIPHERIN, respectively. Furthermore, differentiated cells expressed TRPV1, PAR2, TRPA1, substance P, CGRP, HR1. Using calcium imaging, we observed that a proportion of cells responded to histamine, SLIGKV (a specific agonist of PAR2), polygodial (a specific agonist of TRPA1), and capsaicin (a specific agonist of TRPV1). In conclusion, SKPs are able to differentiate directly into functional SNs. These differentiated cells will be very useful for further in vitro studies.
Keyphrases
- induced apoptosis
- cell cycle arrest
- stem cells
- gene expression
- endoplasmic reticulum stress
- signaling pathway
- spinal cord
- chronic pain
- oxidative stress
- spinal cord injury
- dna methylation
- cell proliferation
- cell death
- cell therapy
- drug induced
- transcription factor
- single cell
- poor prognosis
- pain management
- mesenchymal stem cells
- neuropathic pain
- diabetic rats
- genome wide