Generation of human nociceptor-enriched sensory neurons for the study of pain-related dysfunctions
Preprint
Abstract
In vitro models of the peripheral nervous system would benefit from further refinements to better support studies on neuropathies. In particular, the assessment of pain-related signals is still difficult in human cell cultures. Here, we harnessed induced pluripotent stem cells (iPSCs) to generate peripheral sensory neurons enriched in nociceptors. The objective was to generate a culture system with signaling endpoints suitable for pharmacological and toxicological studies. Neurons generated by conventional differentiation protocols expressed moderate levels of P2X3 purinergic receptors and only low levels of TRPV1 capsaicin receptors, when maturation time was kept to the upper practically-useful limit of 6 weeks. As alternative approach, we generated cells with an inducible NGN1 transgene. Ectopic expression of this transcription factor during a defined time window of differentiation resulted in highly-enriched nociceptor cultures, as determined by functional (P2X3 and TRPV1 receptors) and immunocytochemical phenotyping, complemented by extensive transcriptome profiling. Single cell recordings of Ca 2+ -indicator fluorescence from >9,000 cells were used to establish the “fraction of reactive cells” in a stimulated population as experimental endpoint, that appeared robust, transparent and quantifiable. To provide an example of application to biomedical studies, functional consequences of prolonged exposure to the chemotherapeutic drug oxaliplatin were examined at non-cytotoxic concentrations. We found (i) neuronal (allodynia-like) hypersensitivity to otherwise non-activating mechanical stimulation that could be blocked by modulators of voltage-gated sodium channels; (ii) hyper-responsiveness to TRPV1 receptor stimulation. These findings and several other measured functional alterations indicate that the model is suitable for pharmacological and toxicological studies related to peripheral neuropathies.Keywords
All Related Versions
- Published version: Stem Cells Translational Medicine, 11 (7), 727.
This publication has 79 references indexed in Scilit:
- Combined small-molecule inhibition accelerates developmental timing and converts human pluripotent stem cells into nociceptorsNature Biotechnology, 2012
- Chemically defined conditions for human iPSC derivation and cultureNature Methods, 2011
- Assessment of Chemical-Induced Impairment of Human Neurite Outgrowth by Multiparametric Live Cell Imaging in High-Density CulturesToxicological Sciences, 2011
- AF‐353, a novel, potent and orally bioavailable P2X3/P2X2/3 receptor antagonistBritish Journal of Pharmacology, 2010
- Sensitization of Capsaicin and Icilin Responses in Oxaliplatin Treated Adult Rat DRG NeuronsMolecular Pain, 2010
- Cellular and Molecular Mechanisms of PainCell, 2009
- The TRPV1 receptor and nociceptionSeminars in Cell & Developmental Biology, 2006
- Mechanisms of Neuropathic PainNeuron, 2006
- Calcium Channels, Stores, And OscillationsAnnual Review of Cell and Developmental Biology, 1990
- Central post-stroke pain — a study of the mechanisms through analyses of the sensory abnormalitiesPain, 1989