Differential gene expression of neonatal and adult DRG neurons correlates with the differential sensitization of TRPV1 responses to nerve growth factor

• Published in: Neuroscience letters Vol. 500; no. 3; pp. 192 - 196
• Main Authors: Zhu, Weiguo, Oxford, Gerry S.
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier Ireland Ltd 18.08.2011; Elsevier
• Subjects: Age Factors; Animals; Animals, Newborn; Biological and medical sciences; Cells, Cultured; Dorsal root ganglion; ERK1/2; Fundamental and applied biological sciences. Psychology; Ganglia, Spinal - drug effects; Ganglia, Spinal - growth & development; Ganglia, Spinal - metabolism; Gene Expression Profiling; Gene Expression Regulation; Ion channels; Microarray; Nerve Growth Factor - pharmacology; Nerve Growth Factor - physiology; Neurons - drug effects; Neurons - metabolism; Oligonucleotide Array Sequence Analysis; PI3K/P110α; Rats; Receptor, trkA - physiology; RNA, Messenger - metabolism; Signal Transduction; TRPV Cation Channels - physiology; Vertebrates: nervous system and sense organs; ERK1/2; Ion channels; PI3K/P110α; Dorsal root ganglion; Microarray; Spinal cord; Central nervous system; Nerve growth factor; Ionic channel; Gene expression; TRPV1 vanilloid receptor; Neuron; Spinal ganglion
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2011.06.034

• A microarray analysis of cultured adult or neonatal rat DRG neurons was conducted. • Signaling molecules and ion channels had higher mRNA levels in adult rat DRG neurons. • ERK1/2 and PI3K/P110α had higher mRNA and protein levels in adult rat DRG neurons. • Up-regulation of signaling molecules might explain sensitizing TRPV1 by NGF in adult. Cultures of neonatal and adult dorsal root ganglion (DRG) neurons are commonly used in in vitro models to study the ion channels and signaling events associated with peripheral sensation under various conditions. Differential responsiveness between neonatal and adult DRG neurons to physiological or pathological stimuli suggests potential differences in their gene expression profiles. We performed a microarray analysis of cultured adult and neonatal rat DRG neurons, which revealed distinct gene expression profiles especially of ion channels and signaling molecules at the genomic level. For example, Ca 2+-stimulated adenylyl cyclase (AC) isoforms AC3 and AC8, PKCδ and CaMKIIα, the voltage-gated sodium channel β1 and β4, and potassium channels K v1.1, K v3.2, K v4.1, K v9.1, K v9.3, K ir3.4, K ir7.1, K 2P1.1/TWIK-1 had significantly higher mRNA expression in adult rat DRG neurons, while Ca 2+-inhibited AC5 and AC6, sodium channel Na v1.3 α subunit, potassium channels K ir6.1, K 2P10.1/TREK-2, calcium channel Ca v2.2 α1 subunit, and its auxiliary subunits β1 and β3 were conversely down regulated in adult neurons. Importantly, higher adult neuron expression of ERK1/2, PI3K/P110α, but not of TRPV1 and TrkA, was found and confirmed by PCR and western blot. These latter findings are consistent with the key role of ERK and PI3K signaling in sensitization of TRPV1 by NGF and may explain our previously published observation that adult, but not neonatal, rat DRG neurons are sensitized by NGF.