Sensory neurons are distinguished by distinct signaling networks and receptive characteristics. Thus, sensory neuron types can be defined by linking transcriptome-based neuron typing with the sensory phenotypes. Here we classify somatosensory neurons of the mouse dorsal root ganglion (DRG) by high-coverage single-cell RNA-sequencing (10 950 ± 1 218 genes per neuron) and neuron size-based hierarchical clustering. Moreover, single DRG neurons responding to cutaneous stimuli are recorded using an in vivo whole-cell patch clamp technique and classified by neuron-type genetic markers. Small diameter DRG neurons are classified into one type of low-threshold mechanoreceptor and five types of mechanoheat nociceptors (MHNs). Each of the MHN types is further categorized into two subtypes. Large DRG neurons are categorized into four types, including neurexophilin 1-expressing MHNs and mechanical nociceptors (MNs) expressing BAI1-associated protein 2-like 1 (Baiap2l1). Mechanoreceptors expressing trafficking protein particle complex 3-like and Baiap2l1-marked MNs are subdivided into two subtypes each. These results provide a new system for cataloging somatosensory neurons and their transcriptome databases.
Neurons express a higher number of genes than any other cell type, resulting in the high heterogeneity of neuron subtypes. The pseudo-unipolar sensory neurons of the dorsal root ganglion (DRG) transmit peripheral signals to the spinal cord. Small diameter DRG neurons give rise to unmyelinated axons (C-fibers) and thinly myelinated axons (Aδ-fibers) that convey the nociceptive, thermal and mechanoreceptive signals generated at peripheral nerve terminals to neurons in lamina I-II of the spinal cord. Large DRG neurons transmit mechanoreceptive and proprioceptive signals via thickly myelinated afferents (Aβ-fibers) to spinal lamina III-V1. Traditionally, small neurons have been classified into three subsets: isolectin B4 (IB4)-positive (non-peptidergic, NP) subset, peptidergic (PEP, IB4 negative) subset expressing neuropeptide substance P and calcitonin gene-related peptide (CGRP), and tyrosine hydroxylase (TH)-expressing subset, while large neurons express neurofilament 200 (NF200)2,3,4,5.
Cutaneous mechanoreceptors (MRs), nociceptors, thremoreceptors and itch receptors have been physiologically characterized5,6. Many nociceptors respond to multiple stimulus modalities, whereas others have more specialized response properties. Defined nociceptor subtypes have been termed C-fiber (C-) or Aδ-fiber (A-) mechanoheat nociceptors (MHNs), mechanical nociceptors (MNs), mechanically insensitive (MI) or sensitive afferents, and mechanoheat-cold nociceptors5,6. The molecular properties of DRG neurons have been extensively studied, including their expression of various receptors and ion channels such as neuropeptide Y (NPY) receptors7, MAS-related G-protein-coupled receptors (MRGPRs)8,9, voltage-gated Na+ channels10, transient receptor potential (TRP) channels11,12, ATP receptors13, acid-sensing ion channels (ASICs)14,15 and tyrosine kinase receptors (TRKs)16. Gene expression profiles of DRG tissue have been also analyzed by microarray and RNA-sequencing (RNA-seq) techniques17,18. Although these methods have helped to identify the expression of neuromodulators such as natriuretic peptide B (NPB)19 and regulators of Na+, K+-ATPase (NKA), including the γ-subunit of NKA (FXYD domain-containing ion transport regulator 2, Fxyd2)20,21,22, they cannot provide a global view of the transcriptional profiles of individual neurons.
Recently, multiple efforts have been made to analyze the transcriptional profiles of DRG neurons. The transcriptional profiles of TRPV1 lineage and Nav1.8 channel-expressing DRG neurons have been examined by RNA-seq23,24. By single-cell PCR, Chiu et al. identified six subgroups of DRG neurons25. Single-cell RNA-seq enables a better understanding of a cell's transcriptome26,27,28,29,30,31,32,33. Usoskin et al. performed low-coverage single-cell RNA-seq (3 574 ± 2 010 genes per neuron) and classified the mouse DRG neurons into two PEP types, three NP types, TH type and five NF200-positive types within the traditional classification framework34. However, this method resulted in transcriptional variation among DRG neurons due to the limited number of genes detected in each neuron. These studies are useful resources for analyzing the molecular determinants of sensory neuron types, but their interpretation is complicated by the large variation present within a neuron type defined by a given molecular marker. Moreover, the related functional phenotypes of the neurons have not been experimentally analyzed.
Here, by integrating single-cell techniques such as high-coverage RNA-seq (10 950 ± 1 218 genes per neuron), in vivo patch clamp recording and single-cell PCR, we classify mouse DRG neurons into 10 types and 14 subordinate subtypes with distinct transcriptional patterns, molecular markers and functional annotations, revealing a new catalog of somatosensory receptors. Our single-cell RNA-seq-based clustering reveal more neuron types and subtypes than previous classifications of DRG neurons, and demonstrate that traditional neuron subset-specific markers in fact label multiple neuron types. Moreover, our study suggests that based on the current understanding of molecular function and signaling networks, transcriptome data can partially predict the functions of neuron types. Further, neuron type-specific functional analyses are needed to confirm and elaborate the precise functions of these neuron types. Thus, neuron types can be defined by integrating their transcriptomic, morphological and functional characteristics.
Neuron sampling and quality control of transcriptomic data
RNA-seq analysis showed that the transcriptomes of lumbar 5 (L5) DRG from five adult male mice were homogenous (Supplementary information, Figure S1A and S1B). Immunostaining of CGRP and NF200, combined with IB4 fluorescent labeling showed that ∼35% of neurons were positive for IB4, ∼41.2% were positive for CGRP and ∼46.4% were positive for NF200 (Figure 1A). Approximately 20% of IB4-positive neurons expressed CGRP, whereas ∼5.6% expressed NF200. Approximately 28% of CGRP-positive neurons expressed NF200. A small number of neurons were triple labeled.
A DRG-specific approach was designed to increase the efficiency of single-cell RNA-seq used for neuron typing. First, IB4-positive neurons were identified among neurons freshly dissociated from lumbar DRG by IB4 fluorescence labeling (Figure 1B). Under a microscope, neurons without identifiable satellite cells attached to the cell surface were selected and aspirated with glass pipettes. IB4-positive small neurons, IB4-negative small neurons (cross-sectional area < 800 μm2) and large neurons contributed ∼1/3 of the selected neurons. The total number of neurons used was determined by the results of transcriptomic analysis. We profiled neurons until the number of neuron clusters extracted from the data plateaued and the correlation among neurons stabilized. Sequencing libraries were constructed from the cDNA of 203 neurons collected from 19 mice.
To ensure quality of the samples, FPKM (fragments per kilobase of transcript per 106 mapped reads) values for house-keeping genes actin B (Actb) or glyceraldehyde-3-phosphate dehydrogenase (Gapdh) in each neuron were required to be around 4 675 ± 3 456 (mean ± SD) or 367 ± 268, respectively. Datasets for the corresponding 197 neurons, including 64 IB4-positive neurons, 69 IB4-negative small neurons and 64 large neurons, were processed for transcriptome analysis.
To obtain single-neuron transcriptomes, we examined the correlation between sequencing depth and the number of genes. We found that 1, 5, 10, 20, 30 and 40 million mapped reads per neuron detected 8 906 ± 79, 9 781 ± 127, 10 158 ± 133, 11 142 ± 223, 11 450 ± 256 and 11 694 ± 288 genes, respectively (n = 3, Supplementary information, Figure S2A). The number of mapped reads for each detected gene correlate linearly with the total number of mapped reads (Supplementary information, Figure S2B). Thus, the probability of detecting low-abundance genes depends on the depth of RNA-seq. Therefore, 30 million reads was considered the minimum number of mapped reads to achieve maximal mapping while maintaining efficiency. The average number of mapped reads was 58.2 million (ranging from 29.6 to 106.4 million) for a single neuron (Figure 1C). The number of detectable genes for each neuron ranged from 7 972 to 13 960 (10 950 ± 1 218) per neuron and 20 794 in total (Figure 1D; Supplementary information, Figure S2C). To evaluate the effect of sequencing depth on gene number, six neurons were resequenced to a depth of 181 million reads – three times more than the average sequencing depth for all neurons. The libraries obtained from deeper sequencing runs shared 99.8% similarity with the libraries obtained by lower depth sequencing of the same neuron (Figure 1E). Thus, a sequencing depth of 30 million FPKM was sufficient.
Finally, to examine the quality of RNA-seq, cDNA from one neuron was divided into two equal parts and processed for RNA-seq. The transcriptomic datasets of two libraries derived from the same neuron shared 99.4% similarity (Figure 1F), suggesting a high quality of RNA-seq.
Gene modules identified by weighted gene co-expression network analysis
We performed principal component analysis on all 197 single-neuron transcriptomes as previously reported32. Genes with the highest loading in the first three principal components were analyzed by unsupervised hierarchical clustering. On the basis of this clustering, 2 043 differentially expressed genes were identified (≥ fivefold change, false discovery rate (FDR) < 5%) from 20 794 genes.
Weighted gene co-expression network analysis (WGCNA) is a method used to cluster highly interconnected genes into gene modules35 that could be relevant for cell typing because highly correlated genes are likely to be detected in cells of the same cluster. The module eigengene (ME) is the first component of a given module and is considered to be the most representative gene expression in the module. The module membership of each gene, also known as eigengene-based connectivity (kME), is determined by correlating the gene expression profile with the ME and is highly related to the intramodular connectivity35. The most highly connected gene (i.e., the hub gene) inside the module tends to have high connectivity and a high kME. Performing WGCNA on the 2 043 differentially expressed genes identified 12 gene modules (Figure 1G; Supplementary information, Table S1). The yellow module has a strongly connected gene co-expression network, of which the gene encoding NPB (Nppb) is a hub gene (kME = 0.930). The MEs include genes for the oncostatin M receptor (Osmr), interleukin 31 receptor A (Il31ra), 5-hydroxytryptamine (serotonin) receptor 1F (Htr1f), neurotensin (Nts) and somatostatin (Sst, Supplementary information, Table S1). This network may be related to with itch because IL31RA mediates T-helper cell dependent itch36, and OSMR acts as its heterodimer receptor37. The red module contains genes for peptides such as adenylate cyclase activating polypeptide 1 (Adcyap1, a hub gene; kME = 0.908), galanin (Gal) and tachykinin 1 (Tac1). Genes such as transmembrane protein 176A (Tmem176a) and 176B (Tmem176b), NPY receptor 1 (Npy1r), somatostatin receptor 2 (Sstr2), zinc-finger CCHC domain-containing 12 (Zcchc12) and TRP cation channel, subfamily V, member 1 (Trpv1) are the MEs of red module.
In the pink module, the gene for adenosine A2b receptor (Adora2b, kME = 0.874) is the hub gene; and genes for cerebellin 1 precursor protein (Cbln1), MRGPR B4 (Mrgprb4) and A3 (Mrgpra3), musculoskeletal, embryonic nuclear protein 1 (Mustn1) and protein tyrosine phosphatase, non-receptor type 6 (Ptpn6) are closely associated (Supplementary information, Table S1). In the black module, genes for family with sequence similarity 19, member A4 (Fam19a4) and TH (Th) serve as hub genes (kME = 0.920 and 0.904, respectively), whereas the genes for zinc-finger protein 521 (Zfp521), cholecystokinin A receptor (Cckar) and POU domain, class 4, transcription factor 2 (Pou4f2) are among the MEs (Supplementary information, Table S1). In the turquoise module, MEs include genes for secretogranin III (Scg3, kME = 0.934), cortexin 3 (Ctxn3, kME = 0.930), CD24a antigen (Cd24a, kME = 0.917), CD55 antigen (Cd55, kME = 0.916), synaptoporin (Synpr, kME = 0.915), coiled-coil domain-containing protein 68 (Ccdc68, kME = 0.892) and MRGPRD (Mrgprd, kME = 0.889).
The blue module is characterized by genes encoding the S100 protein, beta polypeptide (S100b, kME = 0.934, the hub gene) and contain MEs such as tubulin alpha 4a (Tuba4a), ly6/neurotoxin 1 (Lynx1), copine VI (Cpne6), FXYD7 (Fxyd7), potassium voltage-gated channel, shaker-related subfamily member 1 (Kcna1) and neurofilament, heavy polypeptide (Nefh) encoding NF200 (Supplementary information, Table S1). The hub genes in the green module encode BAI1-associated protein 2-like 1 (Baiap2l1, kME = 0.922) and neurotrophic TRK type 2 (Ntrk2, kME = 0.911), whereas the MEs include genes for 5-hydroxytryptamine receptor 1D (Htr1d), potassium channel subfamily K member 1 (Kcnk1), Ca2+-dependent activator protein for secretion 2 (Cadps2), calcium channel, voltage-dependent, T type, alpha 1H subunit (Cacna1h) and N-terminal EF-hand calcium-binding protein 2 (Necab2). The green module thus represents large neurons expressing Ntrk216. The purple module contain the parvalbumin gene (Pvalb), a marker of large proprioceptive neurons38, and the MEs include neurexophilin 1 (Nxph1).
In situ hybridization (ISH) confirmed the expression of Il31ra (yellow module), Tmem45b (turquoise module) and Fam19a4 (black module) in small neurons; Nxph1 (purple module) and Tmem176b (red module) in small and some large neurons; Cpne6 and S100 calcium-binding protein A16 (S100a16, blue module) as well as Pvalb (purple module) in large neurons and a subset of small neurons, and Baiap2l1 (green module) in large neurons (Figure 1H; Supplementary information, Figure S3A). Thus, the above gene modules are present in DRG neurons. The genes in brown module, including sclerostin domain containing 1 (kME = 0.973, Sostdc1), fatty acid-binding protein 7 (kME = 0.944, Fabp7), ATPase, Na+/K+ transporting, beta 2 polypeptide (kME = 0.779, Atp1b2) and TIMP metallopeptidase inhibitor 3 (kME = 0.660, Timp3), are found in satellite cells (Supplementary information, Figure S3B). Genes in the magenta module are not highly connected. Genes in the green-yellow modules are expressed in blood cells, and genes in the grey module are considered to be non-module genes. In total, WGCNA identifies eight neuronal gene modules and one glial gene module.
Ten clusters revealed by neuron size-based hierarchical clustering
To analyze the neuronal clusters, 1 745 differentially expressed genes (≥ 5-fold change, excluding 185 eigengenes of satellite cells (brown module, kME > 0.6), all 71 genes of grey module and 42 genes of green-yellow module) from 197 neurons were subjected to principal component analysis. Unsupervised hierarchical clustering analysis was performed on genes with the highest loadings in the first three principal components. This unbiased approach detects eight cell populations (Supplementary information, Figure S4). Each cluster (C) is named in accordance with the average area of its clustered neurons (Supplementary information, Figure S4). Gal-containing small neurons are sorted into C1, whereas exceptionally large neurons in the same cell population are separated into C10. C7 neurons are segregated from C8 neurons in the same cell population because they are only weakly correlated. Thus, we here identified 10 clusters in the hierarchical neuronal matrix, including small neurons (averaged area: ∼267-733 μm2) in C1-C6 and large neurons (averaged area: ∼779-1 257 μm2) in C7-C10 (Figure 2A). The clusters C1-C6 and C8-C10 emerge within the first 98 neurons included for analysis, whereas C7 is detectable only when the number of neurons is doubled.
A cell-cell correlation matrix based on 1 745 differentially expressed genes reveal that C9 neurons are highly correlated among themselves (value of Spearman correlation (VSC): 0.780 ± 0.007), followed by C5 (0.726 ± 0.002), C7 (0.705 ± 0.012), C4 (0.700 ± 0.007), C8 (0.681 ± 0.002), C2 (0.671 ± 0.006) and C3 (0.659 ± 0.020) neurons (Figure 2A). Small neurons in C1 and C6 are moderately correlated (VSC: 0.618 ± 0.003 and 0.574 ± 0.011, respectively). The correlation among neurons in a cluster suggests the intra-cluster homogeneity of neurons, making them more likely to comprise a specific subtype. The correlation matrix also showes the correlation between neurons within different clusters (Figure 2A). C4 neurons are closely correlated with C5 neurons (VSC: 0.578 ± 0.001), whereas large neurons in C8 and C9 are weakly correlated with C1 and C3, respectively (Figure 2A). These inter-cluster correlation patterns could represent the molecular basis of responses by multiple neuron clusters to a specific stimulus.
We next correlated the MEs (kME > 0.700) identified by WGCNA with neuron clusters. Generally, the MEs of red module (kME > 0.600) are found in C1 and C10, yellow module in C2, black module in C3, pink module (kME > 0.500, Mrgpra3 (kME = 0.566)) in C4, turquoise module in C5, magenta module in C7 (kME > 0.600), blue module in C8 and green module in C9 (Figure 2B). Analysis of the eigengenes of each cluster reveals Gal, Adcyap1 and Npy1r for C1; Nppb, Il31ra, Sst and Htr1f for C2; Th, Fam19a4, Zfp521 and Cckar for C3; and Adora2b, Mrgprb4 and Mrgpra3 for C4 (Figure 2B; Supplementary information, Table S1). Mrgprd and the gene encoding lysophosphatidic acid receptor 3 (Lpar3) are the eigengenes for C5; Nxph1 for C7; and S100b, trafficking protein particle complex 3-like (Trappc3l), Cingulin-like 1 (Cgnl1), Cpne6 and Nefh for C8. The eigengenes of C9 included Ntrk2 and genes encoding Baiap2l1, Necab2 and Cadps2. Thus, differential expression of the eigengenes is important for the formation of neuron clusters.
Fourteen neuron subclusters and the “hybrid state”
According to the cluster tree, C1, C2, C4, C5, C6, C8 and C9 could be further classified into two subclusters each, forming a total of 14 subclusters (Supplementary information, Figure S4) that are also indicated by the correlation matrix (Figure 2A). Neuron subclusters can be generated by additional gene networks in the same gene module. The neuron correlation matrix showes that small neurons in C4 can be further divided into two subclusters, C4-1 and C4-2 (Figure 3A). The differential genes shown in the corresponding module of WGCNA reveals that C4-1 neurons express Mrgpra3, whereas C4-2 neurons express both Mrgpra3 and Mrgprb4 (Figure 3A). Both single-cell real-time PCR of the sequenced neurons in C4 and double-fluorescent ISH proved the existence of the C4 subclusters (Figure 3B-D). Mrgprb4 is present in ∼22.1% of Mrgpra3-expressing neurons (n = 104, Figure 3C). The gene co-expression network of Mrgprb4 is separate from that of Mrgpra3, although they are found in the same module (Figure 3E). Thus, this is a canonical case of subclustering based on an additional gene network.
Neuron subclusters can also be formed by the addition of functional genes from other gene modules. Some neurons within a cluster expressed the representative genes of other clusters, a situation referred to “hybrid state.” In this manner, C2 is divided into subclusters C2-1 and C2-2 (Figure 3F). In the corresponding modules of WGCNA, C2-2 neurons expressed Nefh, S100b, Cpne6 and Pvalb (Figure 2B and 3F). The level of Nppb and Il31ra in C2-2 is lower than that in C2-1, and Pvalb and Nefh were expressed strongly in C2-2 but are not detectable in C2-1 as shown by single-cell real-time PCR (Figure 3G). To confirm the existence of C2 subclusters, IB4-negative small neurons (area < 314 μm2), selected randomly from dissociated DRG neurons, were analyzed by single-cell PCR (Figure 3H). We found that Pvalb is expressed in ∼10% of Nppb-containing neurons (n = 30). Double fluorescent ISH proved that Il31ra is co-expressed with S100b and Cpne6 in small DRG neurons (Figure 3I). Thus, C2-1 and C2-2 represent two distinct subclusters, and C2-2 represents a hybrid state. The hybrid state is found to be a property of some clusters or subclusters of small neurons that are genetically correlated with large neurons, suggesting that they might be small neurons with Aδ-fibers (Figure 3J).
The small neurons in C1 are correlated with the large neurons in C8. C8-2 neurons are correlated moderately with C1-1 neurons and weakly with C1-2 neurons (Supplementary information, Figure S5A). Analysis of differentially expressed genes shows that C1-1 neurons express high levels of claudin 9 (Cldn9) and acid-sensitive ion channel 3 (Asic3), whereas C1-2 neurons expressed high levels of Zcchc12 and Sstr2 (Supplementary information, Figure S5B and S5C). C8-1 neurons express high levels of Ntrk3, Ret, Htr1d and Fam19a2, while C8-2 express high levels of Ntrk1, Calca and Htr3a (Supplementary information, Figure S5C).
C5-1 represents a subcluster of Mrgprd-expressing small neurons that also express Gal, Adcyap1 and Tmem176b (Supplementary information, Figure S5D and S5E), suggesting a molecular correlation with C1. The neuron matrix also indicates that C6 neurons are correlated with both C5 neurons and large neurons (Figure 2A). Statistical analysis shows that C6 neurons expressed high levels of Nefh and S100b and a low level of Mrgprd (Supplementary information, Figure S5E and S5F). Double fluoresecent labeling shows that Mrgprd is expressed in S100b- or NF200-containing DRG neurons (Supplementary information, Figure S5G and S5H). These results indicate the “hybrid state” of this neuron cluster.
The correlation of C9-2 with C8 is stronger than that of C9-1 with C8 (Supplementary information, Figure S5I). C9-2 neurons express higher levels of S100b, Asic3 and Cgnl1 but lower levels of Ntrk2, Baiap2l1 and Cadps2 compared with C9-1 (Supplementary information, Figure S5J). In summary, clusters and subclusters of DRG neurons are revealed by analyzing single-cell transcriptome data and the neuronal correlation matrix.
Differential genes of neuron clusters
To identify differentially expressed genes within neuron clusters and subclusters, we compared neuron clusters using the Fisher test. C1 neurons contain high levels of Tac1 and Calca and represented a population of the traditionally classified PEP subset of DRG neurons, whereas C2 expressed a high level of Nppb. Comparisons between C1 and C2 reveal 152 differentially expressed genes (≥ 10-fold change, FDR < 0.05), 83 of which are highly expressed in C1 (e.g., Gal and Adcyap1) and 69 in C2 (e.g., Nppb, Il31ra, Nts and Htr1f; Supplementary information, Figure S6A). Moreover, the representative genes that are differentially expressed between subclusters within C1 and C2 are shown in Supplementary information, Figure S6A. For example, Cldn9 and Asic3 are expressed mainly in C1-1, whereas Zcchc12 and Sstr2 are expressed in C1-2 (Supplementary information, Figure S6A). The expression pattern of C2 also clearly revealed two subclusters.
C3 neurons are Th positive, whereas C4 neurons expressed Mrgpra3 and C5 neurons contained Mrgprd. Traditionally, these neurons are classified as NP small neurons. Comparisons among C3, C4 and C5 neurons revealed representative differentially expressed genes (≥ 10-fold change, FDR < 0.05, Supplementary information, Figure S6B), such as GDNF family receptor alpha 2 (Gfra2), Fam19a4, Zfp521 and Th in C3; Gfra1, Mrgpra3, Mrgprc11 (also known as Mrgprx1), the gene for R-spondin homolog (Rspo1) and Mrgprb4 in C4; and Gfra1, Gfra2, Mrgprd, Lpar3, protein kinase C theta (Prkcq) and Mrgprb5 in C5.
Large neurons in C7, C8 and C9 contained high levels of Nefh. Comparisons among C7, C8 and C9 produce representative differentially expressed genes (≥ 10-fold change, FDR < 0.05, Supplementary information, Figure S7), including Nxph1 and genes for phospholamban (Pln) and wingless-type MMTV integration site family member 7A (Wnt7a) in C7; and Ntrk2, Baiap2l1, Cadps2, Necab2 and the gene encoding Ly6/Plaur domain-containing 1 (Lypd1) in C9. C10 neurons express not only Gal and Adcyap1, the representative genes for C1, but also Th for C3, Rspo1 for C4 and Cpne6 for large neurons.
Markers of neuron clusters
To be considered a marker gene, the prerequisites are selectivity, a relatively high level of expression, and utility in multiple experimental approaches. Gal, Nppb, Th and Mrgpra3 are selected as markers for C1, C2, C3 and C4, respectively. Single-cell real-time PCR show that Gal, Nppb, Th and Mrgpra3 are selectively expressed in C1, C2, C3 and C4 neurons, respectively (Figure 4A). Each cluster could have several markers, e.g., Nts, Il31ra and Htr1f for C2 (Figure 4B) and Cadps2, Baiap2l1 and Necab2 for C9 (Figure 4C). The subclusters C1-1 and C1-2 are marked by Gal together with Cldn9 and Asic3, and Gal combined with Zcchc12 and Sstr2, respectively (Figure 4D). C2-2 is separated from C2-1 by the expression of Pvalb and S100b (Figures 3F-3H and 4D). Both Mrgpra3 and Mrgprb4 are combined markers for C4-2, whereas Mrgpra3 alone is a marker for C4-1 (Figures 3A and 4D).
Mrgprd is expressed highly in C5 and moderately in C6 (Figure 4A and 4D). In Mrgprd-marked C5 neurons, the presence of Gal, Sstr2, Zcchc12, Asic3 and Gfra3 distinguishe C5-1 from C5-2 neurons (Figure 4D and 4E). C6 neurons are distinguished from C5 by their expression of Cpne6 and S100b (Figure 4D). C6-1 contain Gal, whereas C6-2 express Prkcq and Lpar3 at high levels (Figure 4D). Notably, abundant Gal expression is also found in C5-1 and C6-1 neurons. C5-1 differ from Gal-marked C1 by the expression of Mrgprd, whereas C6-1 is differentiated by Mrgprd and high levels of Cpne6 and S100b expression.
For large DRG neurons, Nxph1, Trappc3l and Cadps2 are markers for C7, C8 and C9, respectively (Figure 4D). C8-1 express high levels of Ntrk3 and Htr1d, whereas C8-2 contain high levels of Ntrk1 and Htr3a (Figure 4D and 4E). C9-2 is distinguished from C9-1 by higher levels of Asic3 and Cgnl1 (Figure 4D). The large neurons of C10 express Gal, Th, Rspo1 and Kcnk2 (Figures 4D and 5A).
Traditional markers of neuronal subsets, such as Tac1 and Calca for the PEP subset, IB4 for the NP subset and Nehf for large neurons, are observed in multiple clusters (Figure 4E). IB4 labels C4 and C5 neurons as well as some neurons in C1 and C6. Some IB4-positive neurons in C4 and C5 also express Tac1 and Calca. Moreover, many recently suggested marker genes, such as Cntnap2 (contactin-associated protein-like 2)34, are also found in multiple clusters (Supplementary information, Figure S8A).
The growth factor receptors Ntrk and Gfra are also not restricted to a single neuron cluster. However, differential combinations of Ntrk and Gfra are consistent with the clustering of DRG neurons (Figure 4E). Ntrk1 and Gfra3 are present in C1, C10 and C2 neurons; Ntrk1 and Gfra1 in C4 neurons; Gfra2 and low levels of Gfra1 expression in C5 neurons; Gfra1 and high levels of Ntrk3 expression in C8-1 neurons; Ntrk1 and low levels of Ntrk3 expression in C8-2 neurons, and Ntrk2 and low levels of Ntrk3 expression in C9 neurons.
Double fluorescent ISH was used to examine the distribution of the markers. Il31ra is co-expressed with Nppb but not Gal in small neurons (Figure 4F and 4G). Almost all Th-positive neurons express Fam19a4 and Fxyd6, but not Gal and Nppb (Figure 4H and 4I). Mrgpra3 is not co-expressed with Nppb or Gfra2 (Figure 4J). Mrgprd is not co-expressed with Il31ra in DRG neurons (Figure 4K). S100b is not expressed in Th-positive neurons (Figure 4L), and Pvalb and Th are absent from Ntrk2-positive large neurons (Figure 4M). Thus, markers identified in this study can be used to identify neuron types in DRG tissue.
Functional phenotypes of neuron clusters
We next asked whether neuron clusters represent neurons of different sensory modalities. A heterogeneity analysis of signaling molecules in neuron clusters as well as previous reports implies the functionalities of these neuron clusters (Figure 5A; Supplementary information, Data S1). TRP channels are involved in temperature sensing12. Trpv1 is expressed strongly in C1-1 and moderately in C1-2 and C2-1 (Figure 5A; Supplementary information, Figure S8B). Trpv2 is expressed in almost all clusters but at a low level in C8, whereas Trpv4 is present in some C3 neurons. Trpm8 is expressed in some neurons in C1-2, C6-1 and C8-2, whereas Trpa1 is expressed in C1-2, C4-2, C5-2, C6-2 and C10. Ano1 is present in C2-2 and C7. Thus, several neuron clusters are likely to be differentially sensitive to temperature. The cross-cluster expression of genes encoding mechanoreceptive molecules such as Trpcs, Kcnks, Asic3 and Piezo2 suggests that mechanical stimuli are sensed by neurons in multiple clusters (Figure 5A). The predicted sensitivity of clusters to chemicals depends on the differential expression of chemical receptors (Figure 5A). The differential expression of pruritogen receptors and NPB encoded by Nppb suggests that C2, C4 and C5 selectively transduce itch signals generated by pruritogens (Figure 5A). For example, C4 contains mRNAs encoding the histamine H1 receptor (Hrh1), Mrgprc11 and Mrgpra3, and therefore could be specific for histamine-, BAM8-22- and chloroquine-induced itch.
To evaluate the functional phenotypes of neuron clusters, we carried out in vivo whole-cell patch clamp recording of single neurons selected at random in the L5 DRG of mice upon application of a noxious mechanical stimulus (pinch), heat (42-52 °C), cold (ice water) or innocuous mechanical stimulus (brush and pressure) to the plantar skin of the hindpaw. The appropriate peripheral stimulus induced an inward Na+ current and generated an action potential in the responsive neuron (110 of 129 recorded neurons). mRNA diffusing into the internal solution of the recording pipette was collected and processed for single-cell quantitative real-time PCR to evaluate the expression levels of neuron-type markers, including Gal, Zcchc12, Cldn9, Nppb, Nts, Sst, Th, Mrgpra3, Mrgprb4, Mrgprd, Nefh, Pvalb, Nxph1 and Baiap2l1 (Figure 5B). This analysis was successfully carried out for 69 responsive neurons (Figure 5C and 5D).
Cluster sorting showed that C1, C2, C4, C5, C6 and C7 are involved in sensing heat and pinch (Figure 5D) but have different preferred stimuli. Most recorded C1-2 neurons responded to heat and pinch. Over half of the neurons in C6 and C7 were activated by pressure and pinch, whereas most neurons in C4 responded to pinch. Furthermore, these results suggest the sensory selectivity of neuron clusters. C2 neurons responded to heat and pinch but not to pressure. All recorded C3 neurons were stimulated by brush but not heat, and these neurons were also responsive to pressure and pinch. C9 neurons primarily responded to pressure and pinch. Neurons responding to cold are scattered in C2, C4-1 C5 and C6, but none of these neurons were found to respond only to cold. These results suggest that the transcriptional heterogeneity among neuronal clusters contributes to the functional specificity and probability of neurons to respond to cutaneous stimuli. The sensory thresholds of neurons in the same cluster could be different due to intra-cluster diversity in gene networks and their activity states.
Types and subtypes of somatosensory neurons
We defined neuron types by integrating transcriptomic, morphological and functional characteristics. In the hierarchy of pseudo-unipolar DRG neurons, small neurons are sorted into 6 types and 10 subordinate subtypes, whereas large neurons are grouped into 4 types and 4 subordinate subtypes (Figure 6A and 6B). The neuron types are highly related to neuron size (Figure 6B), suggesting a principle of somatosensory organization. Neuron types C6, C7 and C8 and all subtypes therein have not been previously described (Figure 6B). These subtypes are distinguished by the expression of either additional genes or the representative genes of large neurons. Each neuron type and subtype has a distinct pattern of gene expression and several type-selective markers, including many newly defined markers (Figures 4D and 6B). The traditional markers, such as Tac1, Calca, Nehf, IB4, as well as several newly proposed markers, such as plexin C1 (PLXNC1) and lactate dehydrogenase B (LDHB)34, can not uniquely identify specific types of DRG neurons (Figure 6C; Supplementary information, Figure S8A), although Th has been demonstrated to be a marker of one type of MR.
Previous and current experimental data suggest that small neurons in C1, C2, C4, C5 and C6 are generally sensitive to noxious mechanical stimulus and heat, suggesting that they act as MHNs (Figures 5A, 6D and 6E). In addition, they can be further specified into sensory phenotypes. C1, C4, C5 and C6 represent MHNs that are moderately sensitive to innocuous mechanical stimuli such as pressure. C2 may contain MHNs insensitive to innocuous mechanical stimuli (MI) but sensitive to itch-provoking chemicals (itch-sensitive, IS). C4 and C6 preferentially respond to noxious mechanical stimuli. C4 and C5 are additionally IS neurons acting as MHNs (IS). All MHNs appear to be polymodal nociceptors because they are also chemoreceptive. C3 neurons are the C-fiber low-threshold MR (C-LTMR), which are also sensitive to noxious mechanical stimuli but not to heat. Large DRG neurons are categorized into four types, including C9 as MNs. C7 contains MHNs that are highly sensitive to both noxious and innocuous mechanical stimuli (mechanically sensitive, MS). C8 neurons are typical MRs because the thermoceptive channel Trps is mostly absent in this type.
Moreover, C1, C2, C4, C5, C6, C8 and C9 are further classified into 14 subtypes (Figure 6B). C1-2 neurons are highly sensitive to both heat and noxious mechanical stimuli, whereas C1-1 could be more mechanoreceptive (Figures 5A and 6D). C4-2 neurons are sensitive to massage-like stroking, which is mediated by the MRGPR B4-signaling network, whereas C4-1 neurons are low-threshold mechanoreceptive. C2-2 neurons may be Aδ-fiber MHN (IS). Cold-sensitive neurons are scattered among C2-1, C4-1 and C5, which can also act like MHNs. This classification suggests a new framework for classifying somatosensory neuron types (Figure 6E).
Tissue-specific approach incorporating single-cell RNA-seq for neuron-typing
The present study presents a DRG-specific approach to neuron sampling for neuron typing that incorporates single-cell RNA-seq with other methods. First, neuron sizes are recorded because the differences between small and large neurons correlate with the projections of afferent fibers in the spinal cord and their functions. The correlation between neuron size and neuron type was proven by transcriptome analysis. Second, the principal neuron subsets classified according to IB4 labeling and their proportions are incorporated into this approach, enabling the maximal coverage of neuron types. One of the technical concerns is the number of sequenced neurons required to cover all neuron types in the DRG. The transcriptome similarity of lumbar DRG in mice and the traditionally classified neuron subsets aided our neuron typing through single-cell RNA-seq in a number of neurons. The required number of neurons was determined by subsequent clustering analysis; most neuron clusters and gene modules of DRG neurons appeared when ∼100 neurons were sequenced. The clusters and, in particular, the subclusters became more apparent when more neurons were analyzed. Therefore, the current knowledge regarding neuronal characteristics is important for the design of tissue-specific approaches for neuron typing.
Neuron-typing with high-coverage single-cell RNA-seq
To characterize the transcriptome, a high-coverage of at least 30 million mapped reads per neuron appears to be adequate to detect the majority of expressed genes. Moreover, the number of detected genes and gene copies in an individual neuron should be confirmed to ensure the data quality of the transcriptome analysis. The complete transcriptome of a single neuron is required to define neuron clusters by integrating WGCNA and neuron hierarchical clustering. A recent study has suggested that low-coverage single-cell RNA-seq (i.e., 0.27 million reads for ∼4 600 detected genes) is sufficient to distinguish cell types, including blood cells, dermal cells and neurons30. Similarly, low-coverage single-cell RNA-seq with a large number of neurons has been applied for cell typing in the mouse DRG34. However, this approach resulted in large variations in transcriptional data and only detected 3 574 ± 2 010 genes per neuron (Supplementary information, Figure S9A and S9B). A large number of genes, including neuron type-specific markers, were not detected by the low-coverage single-cell RNA-seq. For example, some marker genes of C2 neurons, including Sst, Nppb and Il31ra, were not detected in all neurons of the corresponding NP3 population reported by Usoskin et al34, and the representative genes Bmp8a and Gpr139, albeit expressed at a low level in C2 neurons, were absent from the gene list of NP3 (Supplementary information, Figure S9C). Therefore, the low-coverage RNA-seq is not sufficient to identify all representative genes for DRG neuron types, particularly those expressed at low levels, and cannot capture the entire transcriptome of a neuron. In contrast, the transcriptome of individual neurons can be comparatively well characterized by high-coverage single-cell RNA-seq in combination with the methods used to evaluate the quality of datasets. In addition, our data can be used to profile non-coding RNAs and to compare alternative splicing and RNA editing across different types of DRG neurons. Thus, the present study, for the first time, provides the classification of neuron types by comprehensive transcriptome analysis.
DRG neuron types under physiological condition
Neuron types have often been defined by their morphological and/or functional characteristics, with or without the use of molecular markers. Recently, single-cell RNA-seq has been used to identify neuron types in an unbiased manner. We propose that transcriptomic, morphological and functional characteristics are the three major components of a defined neuron type. A specific type of neuron has certain morphological properties, a unique transcriptome and transcriptome-derived signaling networks and markers, and a functional phenotype. Our single-cell RNAseq-based clustering analysis reveals more subtypes of DRG neurons than previously expected. We suggest a new catalog of DRG neuron types, including 6 types and 10 subtypes of small neurons, and 4 types and 4 subtypes of large neurons with single or combined markers. In addition to the well-known neuron types (C1, C3, C4, C5, C9 and C10), our present data indicate that Nppb-marked C2 is an independent neuron type, consistent with other recent proposals25,34. Neuron types C6, C7 and C8, and all corresponding subtypes have not been previously reported.
Our study suggests a new architecture of the classification of DRG neurons. The “NP subset” and “PEP subset” are no longer suitable for defining neuron types because transcriptome analysis clearly shows that IB4-positive (NP) neurons express neuropeptides at various levels, and expression of neuropeptides such as substance P and CGRP is not limited to C1 (PEP) neurons. The transcriptional profiles of TRPV1-lineage DRG neurons and Nav1.8 channel-expressing nociceptors23,24 could be shared by several neuron types. Interestingly, some C1 neurons express high levels of both Trpa1 and Trpv1, whereas C4, C5 and C6 express relatively lower levels of Trpa1. Previous ISH results using digoxigenin (DIG)- or fluorescein-labeled probes showed the co-existence of Trpa1 and Trpv1 in ∼3.6% DRG neurons39, and ISH using sensitive radioisotope-labeled probes showed Trpa1 expression in ∼32.4% DRG neurons40. Thus, to fully characterize these neuron types, it is worth to integrate multiple sources of information including molecular characteristics, physiological functions, and sensory circuits.
The neuron types described here represent the physiological, but not the pathological, states of DRG neurons. The gene expression patterns of DRG neurons are markedly changed in animal models of chronic pain induced by peripheral nerve injury or inflammation17. For example, the number of Gal-expressing DRG neurons is increased after peripheral nerve injury, whereas the expression of Tac1 is reduced. Therefore, neuron types and their markers should be studied independently under pathological conditions in various animal models of disease. Moreover, in addition to the regulation of gene expression, the mechanisms of chronic pain could also relate to the translational and post-translational regulation of proteins.
Functional annotations of neuron types and related gene-networks
The present study shows that transcriptome data can partially predict functions of neuron types. The transcriptomic heterogeneity among DRG neuron types correlates with the somatosensory diversity. Identification of six types of MHN suggests that the sensing of mechanoheat stimuli is a basic function for many nociceptors. These MHNs could be further differentiated by the specific signaling network to sense other stimuli. C1-2 neurons act as major MHNs, consistent with previous reports that Gal is involved in mechanical and thermal nociception41. The mechanoreception of C1-1 may be attributed to the expression of TRPC1, KCNK4 and ASIC3, which mediates both cutaneous and muscle nociception induced by mechanical and acid stimuli14. C6 could be MHNs expressing Trpv2, Trpm8, Trpm3, Trpc1 and Asic3, and respond to a broad range of temperature and mechanical stimuli. C7 as an MHN (MS) expresses not only heat sensor ANO142 and touch-related Trpc1 but also the genes typically expressed in large neurons, such as Cpne6 and Pvalb.
C2, particularly C2-1, are MHNs (MI, IS) that express itch-related NPB43, IL31RA36 and proteinase-activated receptor 2 (PAR2) encoded by F2rl144. The thermal sensitivity of C2 correlates with the presence of Trpv1 and Trpv2 in the Nppb gene network and the role of NBP in thermal hyperalgesia19,45. Both C4 and C5 are MHNs (IS). MRGPR A3 in C4, MRGPR D in C5 and C6, and MRGPR C11 in C2 and C4 are major itch receptors (Figure 5A). The Mrgprb4 gene network in C4-2 could be responsible for detecting gentle touch and massage-like stroking46,47. TRPV2, TRPC3, TRPC6 and Piezo2 in C5 may correlate to C4-2's moderate sensitivity to heat and mechanical stimuli and its contribution to nociceptive behavior47,48.
Our analysis supports the notion that the TH-positive DRG neuron functions as C-LTMR2,49. C3 expresses Th, Fam19a4, Cpne6 and Piezo250. Our finding indicates that C9 neurons are Aβ-MNs, consistent with the early idea regarding Aβ-fiber nociceptive DRG neurons51. C8 neurons differentially express Trpc1, Kcnk4, Asic3 and Piezo2, suggesting their roles in mechanoreception. They were not recorded by our in vivo electrophysiological approach, suggesting that either their receptive fields are not in the plantar skin or they possess other modalities that were not tested, such as other touch modalities and limb proprioception. C3 and C8 are two of the most unique populations of neurons that may serve as mechanoceptors. It might be possible to identify novel mechanoreceptive molecules in these neuron types.
Taken together, our findings indicate that most types of nociceptors respond to multiple stimulus modalities and others have more specialized response properties. Sensing of heat and noxious mechanical stimuli may be a principal function for many types and subtypes of nociceptive small DRG neurons that could also be classified by other somatosensory properties such as itch. Two types of nociceptors more specialized for noxious mechanical stimulus exist in large DRG neurons. Most MHNs are also polymodal nociceptors because they are also sensitive to various chemical stimuli. Thus, our study provides new insights into the biological function of somatosensory neurons, particularly for the nociceptors, and suggests that neuron types are defined by their transcriptomic, morphological and functional characteristics. The transcriptome data of DRG neuron types can be a resource for studying sensory mechanisms and pain therapy.
Materials and Methods
Preparation of single DRG neurons
Lumbar DRGs dissected from adult mice (C57BL/6, male, 8-10 weeks) were digested with 1 mg/ml collagenase type 1A, 0.4 mg/ml trypsin type I and 0.1 mg/ml DNase I (Sigma) in DMEM at 37 °C for 25-30 min, triturated and plated on coverslips. Neurons were treated with fluorescein-labeled IB4 (1:1 000; Vector Lab) for 10 min at room temperature. Cell size was recorded according to the scaleplate of an Olympus microscope (IX72). Single DRG neurons with or without IB4 labeling were randomly selected and aspirated into a glass pipette for single-cell RNA extraction. To minimize the changes in gene expression and meet the quality requirement for cDNA used to construct sequencing libraries, all neurons were collected within 4 h of neuron dissociation.
One technical concern was the number of sequenced neurons required to cover all neuron types in DRG. This was determined by subsequent clustering analysis. In fact, most neuron clusters and gene modules for DRG neurons appeared after ∼100 neurons were analyzed; the clusters and subclusters became more apparent when the number of neurons analyzed was increased.
RNA isolation and library construction
The selected neurons were processed for single-cell RNA extraction and reverse transcription within 1 h and were subjected to cDNA amplification and purification. Single DRG neurons were gently transferred into lysis buffer, and reverse transcription was performed using a SMARTer Ultra Low RNA Kit (Clontech) directly in the cell lysate. Single-cell cDNA was amplified using an Advantage 2 PCR Kit (Clontech) according to the manufacturer's protocol. After cDNA amplification, 50 μl of the sample was subjected to cDNA purification, whereas the remaining sample was kept for single-cell PCR experiments. To construct the sequencing library, we used over 5 ng of the purified cDNA with fragments over 600-bp length from each neuron. Purified cDNA from a single cell was sheared into 150-350-bp fragments by Covaris S2. A TrueSeq DNA library preparation kit (Illumina) was used to prepare the sequencing library according to the manufacturer's protocol.
Sequence alignment and analysis
cDNA library was sequenced using the Illumina sequencing platform (HiSeq 2000). The size of the library was ∼300 bp, and both ends of the library were sequenced to a length of 100 bp. The raw reads were cleaned by removing adaptor sequences, short sequences (length < 35 bp), low-quality bases (quality < 20) and ambiguous sequences (i.e., reads with more than two unknown bases 'N').
Genome mapping is a key step in the analysis. We used tophat v2.0.9 to map the cleaned RNA-seq reads to the mouse mm10 genome with two mismatches, two gaps and one multihit allowed. We utilized the tophat2 splicing algorithm to map reads covering splice junctions, thereby improving the utilization of reads. After genome mapping, cufflinks v2.1.0 was used to quantify gene expression. The gene expression value was normalized by FPKM and adjusted by a geometric algorithm.
For the saturation plot, BAM files were generated from genome alignment and genome annotation (gtf/gff). The gradient reads, such as 1, 3, 5, 10, 20 and 30 million reads, were processed to establish the relationship between mapped reads and mm10 genes. Next, relation between the reads and number of genes in each read gradient was determined. The result is shown as the saturation curve.
WGCNA was performed using custom R scripts to identify gene co-expression modules in the transcriptome values of differentially expressed genes. In brief, a correlation matrix among all pairs of genes was created across the measured samples. Next, an adjacency matrix was constructed by raising the co-expression measure (power = 4), which was a soft-threshold of the correlation matrix. The topological overlap measure (TOM) was calculated based on the adjacency matrix. Then, the genes were hierarchically clustered using 1-TOM as the distance measure, and the modules were determined for the resulting dendrogram.
The ME is the first principal component in a given module. The module membership (kME) of each gene in a module refers to the correlation of the gene expression level between the gene and the ME. The genes with the highest value of module membership were considered to be intramodular hub genes. The gene connection network was visualized using the bioinformatics software Cytoscape (v3.1.1) for complex networks.
Custom R scripts were used to perform hierarchical clustering. To identify the differentially expressed genes in each neuron cluster, the transcriptomic data of all qualified neurons were analyzed using unsupervised hierarchical clustering and Fisher's exact test.
Sequences of the primers used in PCR are provided in Supplementary information, Table S3. For cDNA amplification from a single DRG neuron, 50 μl of the sample was subjected to cDNA purification, and the remaining sample was kept for single-cell PCR experiments. Quantitative PCR was performed using Premix Ex Taq (Takara) on a 7500 Fast Real-time PCR system (Applied Biosystems) according to the manufacturer's protocol. The data were analyzed using 7500 System SDS Software 2.3 (Applied Biosystems) by the standard curve method. The mRNA level was normalized to GAPDH mRNA. The data are presented as the mean ± SEM. The PCR products were analyzed on ethidium bromide-stained 1.5% agarose gels.
For single-cell PCR, individual cells were placed gently into a reaction tube containing reverse transcription reagents and processed according to the manufacturer's protocol (Superscript III, Invitrogen). Subsequently, cDNA was used in separate PCR reactions. The reaction mixture (20 μl) was amplified using Ex Taq (Takara) for 45 cycles. Gapdh was used as a positive control. A negative control was obtained from clean pipettes containing bath solution. The PCR products were analyzed on ethidium bromide-stained 1.5% agarose gels.
In situ hybridization
Lumbar 4 and 5 DRG were dissected from adult male mice and processed for ISH. Probes for Gal, Nppb, Il31ra, Th, Mrgpa3 and Mrgprd mRNA, among other genes, are listed in Supplementary information, Table S4. For ISH, cRNA riboprobes were labeled with DIG. Fresh sections of DRG were fixed with 4% paraformaldehyde in DEPC-PBS for 20 min, then acetylated and prehybridized in hybridization buffer for 3 h at 67 °C. The sections were then incubated with the hybridization buffer containing 1 μg/ml of the antisense probe for 16 h at 67 °C. After hybridization, the sections were incubated in alkaline phosphatase-conjugated sheep anti-DIG antibodies (1:2 000; Roche Molecular Biochemicals). The slides were developed in a solution of 1 μl/ml NBT and 3.5 μl/ml BCIP in alkaline phosphatase buffer.
For double fluorescent ISH, one probe was labeled with fluorescein (FITC), whereas the other was labeled with DIG. Both probes were added to the hybridization buffer. After washing and blocking, the sections were incubated with anti-FITC-HRP (1:4 000) overnight at 4 °C. After washing with TNT buffer, the sections were incubated with TSA-Plus (DNP, 1:100) for 10 min. Then, the sections were washed with TNT and incubated with anti-DIG-AP (1:1 000) and anti-DNP Alexa488 (1:500) in 1% blocking reagent overnight at 4 °C. The sections were washed with TNT and TS8.0, and then were developed with HNPP/FR (1:1:100) in TS8.0.
Adult male mice were fixed with 4% paraformaldehyde and 1% picric acid. To label IB4-positive neurons, cryostat sections of DRG were first incubated with 5 μg/ml IB4 (Vector Laboratories). For triple immunofluorescence, the sections were stained with goat antibodies against GSL (1:1 000; Vector Lab), mouse antibodies against NF200 (1:2 000; Sigma) and rabbit antibodies against CGRP (1:2 000; Dia Sorin), followed by FITC-, Cy3- and Cy5-conjugated donkey secondary antibodies against goat, mouse and rabbit (1:500; Jackson ImmunoResearch). The tissues were examined under a confocal microscope.
In vivo whole-cell patch-clamp recording and neuron classification
Mice were anesthetized with pentobarbital sodium (Nembutal, 50 mg/kg i.p. for initial dose and 20 mg/kg i.p. for supplemental dose). After laminectomy at lumbar levels 2-6, L5 DRG were exposed and isolated from the surrounding tissues. Oxygenated artificial cerebrospinal fluid (ACSF) was dripped periodically onto the surface of the ganglia to prevent drying and hypoxia. Two lumbar vertebrae (lumbar 4 and 6) were clamped. The epineurium covering the DRG was removed under a dissection microscope. The skin was sewn to a ring to maintain a pool of warm oxygenated ACSF. The DRG was continuously superfused at a rate of 3 ml/min by oxygenated ACSF that was preheated by an in-line heater to achieve the desired temperature of 37 °C. The ACSF contained (in mM) 130 NaCl, 3.5 KCl, 24 NaHCO3, 1.25 NaH2PO4, 1.2 MgCl2, 1.2 CaCl2 and 10 dextrose. The solution was bubbled with 95% O2 and 5% CO2, and had a pH of 7.4 and an osmolarity of 290-310 Osm. The vasoconstricting drug (Arg8)-vasopressin (10 μM in oxygenated ACSF, Sigma Aldrich) was applied via a syringe. The vasoconstrictor stopped or substantially reduced the blood flow to the capillary bed in the DRG, thereby preventing bleeding that would otherwise occur after the application of collagenase. Collagenase P (1 mg/ml, Roche Diagnostics) was applied to a local region of the DRG via a pipette located close to the surface. The bath perfusion was turned off for ∼5 min during the application. Repetitive collagenase application was performed until the neuronal cell bodies were loosened from the surrounding connective tissue and cells (4-6 applications for patch clamp recording).
Next, we performed in vivo whole-cell patch clamp recording of randomly selected DRG neurons. The patch pipette (resistance 5-8 MΩ) was filled with an internal solution containing (in mM) 135 K-gluconate, 0.5 CaCl2, 2 MgCl2, 5 KCl, 5 EGTA, 5 HEPES and 5 D-glucose. Somatic stimuli were applied to the plantar skin of the hindpaw. A heat stimulus (30-52 °C; 20 s/stimulus) was applied via a thermal stimulator at an inter-stimulus interval of 90 s. Cold stimulus was applied with ice water (20 s per stimulus). An innocuous brush on the skin was performed using a cotton swab. Innocuous pressure was induced by picking up a fold of skin with a flattened alligator clip to produce a consistent strength (∼6.5 mN/mm2). Noxious mild pinching at the hindpaw was performed using calibrated serrated forceps (∼6 N/mm2). Mechanical stimuli (brush, pressure and pinch) were applied (2 s per stimulus) in ascending order with an inter-stimulus interval of 30 s. Noxious stimulation was applied sparingly to avoid neuronal sensitization.
Whole-cell recordings were performed using an Axopatch 200B amplifier and were digitized with a Digidata 1440A interface and controlled by pCLAMP10.1 software. The whole-cell configuration was obtained in voltage-clamp mode. In brief, we filled a glass electrode with intracellular solution and advanced it quickly to the target depth under moderate positive pressure. When the tip of the electrode was close to a neuron, the tip resistance was increased. We removed the positive pressure and applied negative pressure to aid in seal formation. We achieved the whole-cell configuration using brief bursts of negative pressure to rupture the cell membrane. For detection of responses induced by stimuli, the DRG neuron was subjected to whole-cell recording in voltage-clamp mode at −60 mV. The peripheral stimulus caused a large inward Na+ current and a small outward K+ current, and generated an action potential in responsive neurons.
After recording, the internal solution was collected in a PCR tube containing 2 μl polymerase buffer, 0.5 μl oligo dT primer, 0.5 μl Quantiscript RT enzyme mix (Qiagen) and incubated for 1 h at 42 °C. The cDNA product was treated with 4 μl ligase buffer and 1 μl ligase mix for 30 min at 24 °C, and then amplified with 14.5 μl REPLI-g sc reaction buffer and 0.5 μl REPLI-g SensiPhi DNA polymerase for 2 h at 30 °C according to the manufacturer's instructions (Qiagen). After amplification, the reaction solution was diluted to 300 μl. Then, we performed quantitative real-time PCR to evaluate the gene expression level of markers, including Gal, Zcchc12, Cldn9, Nppb, Sst, Nts, Th, Mrgpra3, Mrgprb4, Mrgprd, Nxph1, Baiap2l1, Pvalb and Nefh. Recorded neurons were sorted into corresponding clusters when the expression level of the marker genes for one cluster was at least fivefold higher than that of other clusters. Recorded neurons were sorted into C6 when several marker genes were detected simultaneously.
The gene data sets are deposited in the public resource Gene Expression Omnibus with accession number of GSE63576.
XZ, H-S X, LB, C-L L and K-C L conceived and designed the study. Y-J L and Y-Q Z collected neurons. B-B Z constructed the library. C-L L, M-M S and RH analyzed RNA-seq data. DW, C-L L, HL, J-R Z, Y-J L and X-Y H performed ISH. C-L L, DW, S-S W and X-Y H performed single-cell real-time PCR. YC performed single cell PCR. DW performed IHC. K-C L recorded neurons. C-L L treated recorded neurons for Q-PCR. XZ, C-L L and LB wrote the manuscript.
Competing Financial Interests
The authors declare no conflict of interest.
Gene Expression Omnibus
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We thank Drs Li Yang and Luo-Nan Chen for comments on data analysis and manuscript. This work was supported by the National Natural Science Foundation of China (31130066 and 81300961) and the Strategic Priority Research Program (B) of Chinese Academy of Sciences (XDB01020300).
( Supplementary information is linked to the online version of the paper on the Cell Research website.)
Transcriptone homogeneity of single DRG from 5 adult mice. (PDF 4771 kb)
Assessment of sequencing depth. (PDF 3691 kb)
Differentially expression of representative genes in module purple, blue and brown. (PDF 8119 kb)
Neuron populations identified by unsupervised hierarchical clustering. (PDF 5214 kb)
DRG neuron subclusters and “hybrid states” of subclusters. (PDF 716 kb)
Differentially expressed genes in clusters of small DRG neurons. (PDF 1562 kb)
Differentially expressed genes in the clusters of large DRG neurons. (PDF 8063 kb)
Transcriptional heterogeneity of the gene expression in DRG neuron types. (PDF 6226 kb)
The comparison between the data from Usoskin et al (Nat Neurosci 2015; 18:145–153, shown as another data) and our data. (PDF 7812 kb)
Gene modules from WGCNA (XLS 1415 kb)
Differentially expressed genes used for WGCNA (XLS 6086 kb)
Primers for PCR (PDF 175 kb)
Primes for in situ Hybridization Probes (PDF 180 kb)
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Li, CL., Li, KC., Wu, D. et al. Somatosensory neuron types identified by high-coverage single-cell RNA-sequencing and functional heterogeneity. Cell Res 26, 83–102 (2016). https://doi.org/10.1038/cr.2015.149
- primary sensory neuron
- neuron type
- single-cell RNA sequencing
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