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PLoS One. 2012; 7(5): e36355.
Published online 2012 May 1. doi:  10.1371/journal.pone.0036355
PMCID: PMC3341357

CGRPα-Expressing Sensory Neurons Respond to Stimuli that Evoke Sensations of Pain and Itch

Hiroaki Matsunami, Editor


Calcitonin gene-related peptide (CGRPα, encoded by Calca) is a classic marker of nociceptive dorsal root ganglia (DRG) neurons. Despite years of research, it is unclear what stimuli these neurons detect in vitro or in vivo. To facilitate functional studies of these neurons, we genetically targeted an axonal tracer (farnesylated enhanced green fluorescent protein; GFP) and a LoxP-stopped cell ablation construct (human diphtheria toxin receptor; DTR) to the Calca locus. In culture, 10–50% (depending on ligand) of all CGRPα-GFP-positive (+) neurons responded to capsaicin, mustard oil, menthol, acidic pH, ATP, and pruritogens (histamine and chloroquine), suggesting a role for peptidergic neurons in detecting noxious stimuli and itch. In contrast, few (2.2±1.3%) CGRPα-GFP+ neurons responded to the TRPM8-selective cooling agent icilin. In adult mice, CGRPα-GFP+ cell bodies were located in the DRG, spinal cord (motor neurons and dorsal horn neurons), brain and thyroid—reproducibly marking all cell types known to express Calca. Half of all CGRPα-GFP+ DRG neurons expressed TRPV1, ~25% expressed neurofilament-200, <10% contained nonpeptidergic markers (IB4 and Prostatic acid phosphatase) and almost none (<1%) expressed TRPM8. CGRPα-GFP+ neurons innervated the dorsal spinal cord and innervated cutaneous and visceral tissues. This included nerve endings in the epidermis and on guard hairs. Our study provides direct evidence that CGRPα+ DRG neurons respond to agonists that evoke pain and itch and constitute a sensory circuit that is largely distinct from nonpeptidergic circuits and TRPM8+/cool temperature circuits. In future studies, it should be possible to conditionally ablate CGRPα-expressing neurons to evaluate sensory and non-sensory functions for these neurons.


Small-to-medium-diameter neurons in the dorsal root ganglia (DRG) have classically been divided into peptidergic and nonpeptidergic subsets [1], [2]. Many of these neurons respond to noxious thermal, mechanical and chemical stimuli, making them nociceptive, whereas others respond to innocuous stimuli, such as warming and cooling. The most widely recognized markers of peptidergic neurons are CGRP and substance P, while IB4-binding and fluoride-resistant acid phosphatase (FRAP; also known as Prostatic acid phosphatase, PAP) classically mark nonpeptidergic neurons [3], [4].

The sensory functions of these circuits were recently examined through the use of sophisticated genetic and physiological techniques. Nonpeptidergic, Mrgprd-expressing neurons are unmyelinated and contribute to mechanosensation but not thermosensation or cold sensation [5], [6]. Peptidergic CGRP+ neurons are myelinated (A-fibers) or unmyelinated (C-fibers) and, depending on fiber type, respond to nociceptive stimuli or guard hair displacement [7], [8]. TRPV1+ neurons, a subset of which are peptidergic [9], detect noxious thermal stimuli and some pruritogens [5], [10], [11], [12], [13]. However, the extent to which the broader class of peptidergic CGRP+ neurons is required for innocuous and noxious stimulus detection in mammals is currently unknown.

CGRP is not a single peptide but two separate peptides (CGRPα and CGRPβ) encoded by separate genes (Calca and Calcb). Calca is alternatively spliced, giving rise to CGRPα in neurons and calcitonin in thyroid C cells [14]. And, CGRPα and CGRPβ are nearly identical at the amino acid level. As a result, antibodies typically cannot distinguish CGRPα from CGRPβ, necessitating use of the term “CGRP-immunoreactivity" (CGRP-IR). CGRP-IR cells and fibers are present in multiple tissues, including the brain, stomach, intestine, skin and bladder [15], [16], [17], [18]. In studies where expression of each gene was resolved, both CGRPα and CGRPβ were expressed in the DRG although CGRPα was expressed at two-fold higher levels [16], [17].

When released peripherally from neurons, CGRPα causes vasodilatation, relaxes smooth muscle cells and contributes to migraine pathogenesis [19]. CGRPα is also released in the dorsal spinal cord and potentiates excitation caused by noxious stimuli and pronociceptive chemicals [20], [21]. CGRPα levels also regulate sensitivity to noxious heat [22]. Notably, CGRPα knockout mice have reduced behavioral responses to capsaicin and impaired heat hyperalgesia although acute heat responsiveness is not affected [23], [24], [25].

To directly study the projections and sensory functions of CGRPα neurons, we generated a knock-in mouse that expresses an axonal tracer and a conditional cell ablation construct from the Calca/Cgrpα locus. We used these mice to prospectively identify peptidergic DRG neurons in culture and show that they respond to agonists that evoke sensations of pain and itch.


CGRPα-GFP+ neurons respond to agonists that evoke sensations of pain and itch

At the time we began this study, there were no ways to prospectively identify CGRP+ sensory neurons for physiological studies. To permit direct visualization of CGRP+ sensory neurons and axons, we knocked-in a floxed (LoxP flanked) membrane-tethered axonal tracer (farnesylated enhanced GFP) to the Calca locus (Fig. 1A) [26]. This floxed GFP also conditionally blocks expression of downstream DTR (Cre recombinase-dependent expression of DTR will be described in a subsequent study). Heterozygous (CGRPα-GFP+/−) mice, which contain one functional Calca allele and one GFP allele, were used throughout this study. The mice were viable and showed no obvious phenotypic or behavioral abnormalities.

Figure 1
CGRPα-GFP+ DRG neurons respond to agonists that evoke pain and itch sensation.

We next loaded cultured DRG neurons from CGRPα-GFP+/− mice with the calcium indicator Fura2-AM. CGRPα-GFP+ neurons were readily identifiable based on intrinsic GFP fluorescence and accounted for 39.9% of all Fura2-loaded neurons (Fig. 1B, arrowheads; n = 1292 Fura2+ neurons analyzed). No CGRPα-GFP+ cells were present from wild-type littermate controls. A majority (54.8%) of these CGRPα-GFP+ neurons were 17–30 µm in diameter, with the remainder being either smaller or larger.

We then monitored calcium responses in all CGRPα-GFP+ and CGRPα-GFP neurons to capsaicin, mustard oil, menthol, icilin, histamine, chloroquine, ATP and acidic pH (Fig. 1C–J, Table 1, Table S1, Table S2). Capsaicin is a ligand for the noxious heat- (>43°C) and acid-sensitive TRPV1 receptor [27] and activated approximately 50% of all CGRPα-GFP+ neurons. Mustard oil, an agonist of the irritant and noxious cold receptor TRPA1, activated 36.8±2.0% of all CGRPα-GFP+ neurons. Menthol, a nonselective modulator of TRPA1 and TRPM8 [28], [29], activated 14.3±5.0% of all CGRPα-GFP+ neurons (Table 1). A low concentration of icilin, which selectively activates TRPM8 [30], activated 2.2±1.3% of all CGRP+ neurons. Histamine and chloroquine evoke the sensation of itch [31] and activated ~11% of all CGRPα-GFP+ neurons. The nonselective P2X and P2Y purinergic receptor agonist ATP activated 12.8±2.2% of all CGRPα-GFP+ neurons. Lastly, lowering the pH to between 5.0 and 6.0 activated 27.0±2.2% of all CGRPα-GFP+ neurons. For all ligands studied, the majority of all CGRPα-GFP+ responsive cells were small- to medium-diameter (Table S1). Taken together, these data indicate that peptidergic CGRPα+ neurons can detect diverse ligands that evoke sensations of pain and itch.

Table 1
Percentage of CGRPα-GFP+/− DRG neurons that respond to agonists that evoke pain and itch.

CGRPα-GFP genetically marks a circuit that is largely distinct from nonpeptidergic and TRPM8+ sensory circuits

To determine if CGRPα-GFP was expressed in peptidergic sensory neurons, we next immunostained sections of lumbar DRG with antibodies to GFP and various neuronal markers. We found that the vast majority (88.9±0.5%) of all CGRP-IR neurons were CGRPα-GFP+ (Fig. 2A–C, Table 2). Conversely, 67.8±0.8% of all CGRPα-GFP+ neurons were CGRP-IR. This lack of complete overlap was likely due to the greater sensitivity of GFP immunostaining—GFP filled cells in their entirety and was easier to detect than CGRP-IR, especially in cells with low levels of CGRP-IR. Interestingly, ~10% of the CGRP-IR neurons did not colocalize with CGRPα-GFP. Because the CGRP antibody we used recognizes CGRPα and CGRPβ, these CGRP-IR-only cells could represent DRG neurons that express CGRPβ alone [16], [17]. In addition, approximately 50% of the CGRPα-GFP+ neurons expressed TRPV1 (Fig. 2D–F, Table 2), consistent with our functional studies above.

Figure 2
CGRPα-GFP colocalizes with peptidergic nociceptive neuron markers.
Table 2
Percentage of CGRPα-GFP+ neurons co-labeled with different markers.

In contrast, there was little (<1%) overlap between CGRPα-GFP and TRPM8 (Fig. 2G–I), a receptor that is activated by icilin, menthol and cool temperatures [32], [33]. There was also limited overlap between CGRPα-GFP and nonpeptidergic markers (IB4 and PAP; Fig. 2J–O, Table 2), which was consistent with previous studies [3], [34]. Some (18.1±0.5%) CGRPα-GFP+ neurons colocalized with neurofilament-200 (NF200) (Fig. 2P–R), a marker of large-diameter neurons with myelinated axons. Importantly, DTR was not expressed in any DRG neurons (Table 2), indicating that the floxed GFP insert effectively blocks downstream transcription.

In the spinal cord, CGRPα-GFP (Fig. 3A) and CGRP-IR (Fig. 3B) were colocalized in lamina I and lamina II outer, with fibers extending into lamina V and towards lamina X. There was little overlap between CGRPα-GFP+ and IB4-binding terminals in lamina II (Fig. 3C, D), revealing segregation between peptidergic and nonpeptidergic spinal circuitry. When taken together, our data indicate that CGRPα-GFP genetically marks a distinct subset of small-to-medium- and large-diameter DRG neurons in adult mice and constitutes a circuit that is largely distinct from nonpeptidergic circuits and TRPM8+/cool temperature-sensing circuits.

Figure 3
CGRPα-GFP axons terminate in dorsal spinal cord.

CGRPα-GFP is expressed in motor neurons and a small population of neurons intrinsic to the dorsal spinal cord

CGRP-IR in the dorsal horn is typically attributed to primary afferent axons and their terminals; however CGRP-IR is also present in a subset of dorsal horn neurons in rats and mice [35], [36]. To detect these cells immunohistochemically, these groups performed dorsal rhizotomies or treated animals with colchicine (colchicine arrests axonal transport, allowing CGRP to accumulate). Scattered Cgrpα/Calca-expressing cells were also detected in the dorsal horn by in situ hybridization, in Allan Brain Atlas adult spinal cord images [37]. The high sensitivity of the membrane-tethered GFP axonal tracer allowed us to detect these intrinsic CGRPα+ neurons without manipulating mice surgically or chemically. When examined at higher magnification, these spinal neurons were located between axon terminals of CGRPα-GFP+ and IB4+ sensory neurons, with CGRPα-GFP+ neurons being predominantly located in lamina II inner and lamina III (Fig. 4A–F, arrowheads). Very few of these intrinsic CGRPα-GFP+ dorsal horn neurons contained PKCγ (Fig. 4C,F), a marker of some lamina II and III neurons [38], [39]. In the ventral horn, CGRPα-GFP labeled many CGRP-IR motor neurons (Fig. 4G–I) along with their axons, which terminate at motor endplates in skeletal muscle (Fig. 5A–C). There were also a number of CGRP-IR motor neurons that lacked CGRPα-GFP, likely reflecting a subset of motor neurons that only express CGRPβ [40].

Figure 4
CGRPα-GFP marks a small population of neurons in lamina II/III and motor neurons in spinal cord.
Figure 5
Glabrous skin montage.

CGRPα-GFP+ neurons innervate cutaneous and visceral tissues

CGRP-IR fibers are present in cutaneous and visceral tissues [16], [18], [26], [41], [42], [43]. Whether these fibers originate from CGRPα- and/or CGRPβ-expressing sensory neurons is unknown. To address this question, we stained a number of peripheral tissues from CGRPα-GFP+/− mice with antibodies to GFP and the pan-nerve fiber marker PGP9.5. We observed CGRPα-GFP+ free nerve endings in the epidermis of glabrous skin (Fig. 5D–I, Fig. 6). Most of these CGRPα-GFP+ endings had a straight and stubby morphology that was distinct from the meandering “zig-zag" shape of PGP9.5+/CGRPα-GFP (presumably nonpeptidergic) fibers. We previously observed this same morphological distinction between peptidergic and nonpeptidergic fibers when targeting farnesylated GFP to Mrgprd+/nonpeptidergic neurons [26]. Interestingly, we also noticed that some of the epidermal CGRPα-GFP+ fibers had small spheres at their tips (see arrowheads, Fig. 5G-inset). These spheres may simply result from membrane budding or intriguingly might constitute a novel transduction unit at the tips of some peptidergic afferents. CGRPα-GFP+ afferents were also present within sweat glands of glabrous skin (Fig. 5G–I). These afferents, which were also PGP9.5+, are likely sensory in origin because CGRPα is not expressed in sympathetic ganglia of mice [17]. In hairy skin, CGRPα-GFP+ fibers progressed through the dermis and terminated in the epidermis and on guard hair follicles (Fig. 5J–L).

Figure 6
CGRP?-GFP+ axons innervate muscle and skin.

In addition, CGRPα-GFP+ fibers were present in the submucosal/smooth muscle layers of the small intestine (Fig. 7A–C), consistent with previous studies [44], [45]. There were also numerous green fluorescent cells in intestinal villi; however, these cells were not CGRPα-GFP+ because: a) they did not co-stain for CGRP-IR (Fig. 7B) and more importantly, b) they were detectable in wild-type mice (i.e., mice lacking GFP; Fig. 7C-inset). These cells are likely a population of autofluorescent stromal cells [46]. There were also a large number of CGRP-IR cells in the intestinal villi that were not CGRPα-GFP+ (Fig. 7B). These CGRP-IR-only cells likely express CGRPβ, particularly given that CGRPβ/Calcb is the primary CGRP gene expressed in the gut [16], [17]. Lastly, we observed CGRPα-GFP+ afferents in the bladder (Fig. 7D–I), a visceral tissue that is innervated by sensory afferents. When taken together, our data indicate that CGRPα-GFP+ neurons innervate diverse cutaneous and visceral structures.

Figure 7
CGRPα-GFP axons and cells in visceral tissues.

CGRPα-GFP labels other cell types that express Calca, including thyroid cells and neurons in the brain

Since GFP was targeted to exon 2 of Calca, an exon that is common to CGRPα and calcitonin [14], CGRPα-GFP should be present in all tissues where Calca is expressed. Indeed, we found that CGRPα-GFP was co-localized with CGRP-IR in parafollicular cells of the thyroid (Fig. 7J–L).

We next thoroughly mapped CGRPα-GFP expression in the brain. To do this, we immunostained adult mouse brain sections and noted all locations where CGRPα-GFP+ cell bodies were found (Table 3). With the exception of the abducens nucleus, Purkinje cells, cuneiform nucleus and the dorsomedial thalamic nucleus, we detected CGRPα-GFP+ cell bodies in all regions previously known to express CGRPα [47], [48], [49], [50]. Representative regions where cellular and/or fiber staining were observed include the spinal trigeminal nucleus caudalis (Fig. 8A), the parabrachial nucleus (Fig. 8B), the peripeduncular and posterior intralaminar thalamic nuclei (Fig. 8C), the subparafascicular nucleus of the thalamus (Fig. 8D), the nucleus accumbens (Fig. 8E), the subiculum (Fig. 8F) and weakly in the visual cortex (Fig. 8F, inset). Calca-GFP BAC transgenic mice produced by the GENSAT project show a similar distribution of cellular and axonal labeling in the brain [51]. Taken together, our data indicate that CGRPα-GFP knock-in mice reproducibly mark all cells and tissues that are known to express Calca.

Figure 8
CGRPα-GFP labels neurons and axons in specific brain regions.
Table 3
Cell body expression of CGRPα-GFP in different brain regions.


We generated the first knock-in reporter mouse to directly visualize and functionally study CGRPα-containing sensory neurons. While characterizing these mice, we found that CGRPα-GFP faithfully marked the peptidergic subset of DRG neurons, as well as other cell types throughout the body that express Calca. In contrast, cells that express Calcb/CGRPβ, including intramural neurons of the intestine [17], were devoid of CGRPα-GFP immunoreactivity. Our reporter mice can thus be used to discriminate Calca-expressing cells from cells that express Calcb. The membrane-tethered GFP reporter allowed us to prospectively identify live CGRPα-expressing neurons in culture for functional studies. Remarkably, half (~50%) of all CGRPα-GFP+ DRG neurons expressed TRPV1 and half of all CGRPα-GFP+ DRG neurons responded to the TRPV1 agonist capsaicin, suggesting that CGRPα+ neurons may play a significant role in capsaicin and noxious thermal sensitivity in vivo. In addition, >50% of all histamine- and chloroquine-responsive neurons were CGRPα-GFP+, suggesting a major role of CGRPα-expressing neurons in histamine-dependent and histamine-independent itch. Likewise, there is a large degree (~90%) of overlap between TRPV1/capsaicin-responsive neurons and histamine-responsive neurons [31], [52], suggesting thermal pain and histamine-dependent itch are encoded by the same class of sensory neurons.

We found little (<1%) overlap between CGRPα-GFP+ cells and TRPM8. And, very few (2%) CGRPα-GFP+ cells were activated by the cooling agent icilin (at a concentration that preferentially activates TRPM8 [30]). Likewise, others found no overlap between CGRP-IR and Trpm8-expression in DRG [32], [53], and no CGRP-IR neurons responded to cooling in electrophysiological studies [7]. These results collectively suggest segregation between CGRP and cool temperature-sensing/TRPM8+ circuits.

In contrast, Takashima et al. found that TRPM8-GFP and CGRP-IR overlap by ~20% when using a BAC transgene to mark Trpm8-expressing neurons [54]. BAC reporters often drive higher levels of gene expression when compared to knock-in reporters, but can suffer from position effects that compromise expression specificity [51]. Thus, higher detection sensitivity and/or position effects could explain why there was a greater degree of overlap between CGRP-IR and BAC reporter driven Trpm8 expression than we and others observed when examining endogenous Trpm8 expression.

We also found that 14.3±5.0% of all CGRPα-GFP+ cells were menthol-responsive. Contrary to what is commonly stated in the literature, menthol is not a TRPM8 specific agonist. Menthol activates TRPA1 at sub- to low-micromolar concentrations and inhibits TRPA1 at higher concentrations [28], [29]. This bimodal modulation provides one of many explanations for why a smaller percentage of CGRPα-GFP+ neurons responded to menthol in culture than to the TRPA1 agonist mustard oil (Table 1).

With regard to position effects, it will be interesting to determine if the Calca-GFP BAC transgenic mouse line made by the GENSAT project reproduces CGRPα expression in DRG, brain and peripheral tissues to the same extent as our knock-in mouse [51]. In addition, it will be interesting to determine if this BAC transgenic line distinguishes Calca-expressing cells from Calcb-expressing cells. Calca and Calcb are located ~80 kb apart in the mouse genome. This genomic proximity could contribute to their similar but not identical expression patterns. Baillie and colleagues recently used Calca-GFP BAC transgenic mice and optical imaging techniques to visualize an axon reflex in an individual CGRPα+ sensory afferent [55].

In what is perhaps the most comprehensive physiological study of CGRP+ sensory neurons to date, Lawson and colleagues found that CGRP-IR neurons can be classified as C-fiber and Aδ-fiber nociceptive units (responsive to noxious thermal and high threshold mechanical stimuli), unresponsive C-fibers or Aα/β guard hair afferents. None of the CGRP-IR neurons had C-cooling/cold or C-low threshold mechanoreceptive (C-LTMR) properties. These findings, combined with TRPV1 cell inactivation studies (described above) and our current work, consistently point to a role for CGRP+ neurons in sensing noxious heat.

CGRPα-GFP might also mark the CGRP-IR+ Aα/β guard hair units that were identified by Lawson and colleagues [7], particularly since CGRPα-GFP+ fibers terminated on guard hairs in hairy skin and ~25% of all CGRPα-GFP+ neurons expressed NF200, a marker of myelinated afferents. Guard hairs add sheen to the coat of furry mammals, are often water repellent, and drive activity in sensory afferents when deflected [7], [56], [57]. Whether activation of guard hair afferents has sensory and/or non-sensory functions in mammals is currently unknown.

Ultimately, it should be possible to directly evaluate the in vivo functions of CGRPα+ sensory neurons by taking advantage of the LoxP-stopped DTR that we knocked-in immediately behind GFP (Fig. 1A). DTR, when combined with injections of diphtheria toxin, can be used to conditionally ablate cells and neurons in adult mice [5], [58]. Importantly, DTR expression was completely blocked in DRG (Table 2). We engineered DTR so that its ATG start codon will precisely substitute for the start codon of GFP upon CRE recombinase-mediated excision. DTR should thus be expressed in all cell types that jointly express CGRPα and CRE recombinase (including cells that expressed CRE at any time during development). When crossed with sensory neuron selective lines, such as Nav1.8-Cre or Advillin-Cre [59], [60], [61], [62], this could permit selective expression of DTR in DRG neurons while maintaining GFP expression in all other Calca-expressing cell types. Given that Calca is expressed in many other cell types, this strategy could be broadly employed to genetically label, ablate and study the function of diverse peptidergic CGRPα-containing cell types throughout the brain and body.

Materials and Methods

All procedures and behavioral techniques involving vertebrate animals were approved by the Animal Care and Use Committee at the University of North Carolina at Chapel Hill.

Molecular Biology

Recombineering was used to generate Calca targeting arms from a C57BL/6-derived bacterial artificial chromosome (BAC; RP24-136021). The start codon located in exon 2 is common to CGRPα and calcitonin and was replaced with an AscI site to facilitate cloning of an axonal tracer and a conditional cell ablation construct: AscI-LoxP-EGFPf-3x pA-LoxP-DTR-pA-Frt-PGK-NeoR-Frt-AscI. EGFPf = farnesylated enhanced GFP [26]. DTR = human diphtheria toxin receptor [58]. NeoR = neomycin resistance. The LoxP sites were oriented so that the first ATG encountered was in GFP or, after Cre recombinase-mediated excision, DTR. Correct targeting was confirmed in 5.8% of all embryonic stem cell clones by Southern blotting using flanking 5′ and 3′ probes and a NeoR internal probe. High percentage chimeras were crossed to C57BL/6 females to establish germline transmission and then crossed to ACTFLPe mice (B6.Cg-Tg(ACTFLPe)9205Dym/J, Jackson Laboratory) to remove the Frt-flanked selection cassette (removal confirmed by PCR). Next, mice were backcrossed to C57BL/6 to remove the ACTFLPe allele (removal confirmed by PCR) and then backcrossed to C57BL/6 mice for 8 generations to establish the CGRPα-GFP knock-in line. As a technical note, we were only able to detect GFP expression in DRG neurons after removal of the PGK-NeoR selection cassette.

Calcium Imaging

Adult (4–6 week old) male CGRPα-GFP+/− mice were decapitated, DRG were dissected then neurons were dissociated using collagenase (1 mg/mL; Worthington, CLS1) and dispase (5 mg/mL; Gibco, 17105-041) in DH10 media (1[ratio]1 Ham's DMEM/F12, 10% FBS and 1% penicillin/streptomycin) [63], [64]. Medium was supplemented with 25 ng/mL of glial-derived neurotrophic factor (GDNF; Upstate, GF030). The neurons were plated onto coverslips coated with 0.1 mg/mL poly-D-lysine and 5 µg/mL laminin. After 24 h, neurons were washed 2× with Hank's balanced salt solution (HBSS) and incubated for 1 h with 2 µM Fura2-AM in the dark at room temperature. Next, the cells were washed 3× with HBSS and maintained at room temperature for 30 min prior to imaging. After a 60 s baseline, agonists (1 µM capsaicin, 100 µM mustard oil, 200 µM menthol, 4 µM icilin, 100 µM ATP, 100 µM histamine, 1 mM chloroquine or acidic pH 5–6 HBSS) were perfused onto the neurons. Following activation, cells were perfused with HBSS to remove the agonist, which was followed by addition of 100 mM KCl to determine the total number of neurons present. Images were acquired on a Nikon Eclipse Ti microscope (Nikon, Melville, NY). GFP+ neurons were identified by eye, and then a 500 ms exposure was used to image the cells. CGRPα-GFP+ neurons of all sizes were included in the analysis. Following addition of agonist, only neurons with responses greater than 15% of baseline were scored as responders.


Mice were sacrificed by overdosing with pentobarbital. The thyroid, brain, bladder, hindpaw skin, lumbar DRG, lumbar spinal cord and small intestine were dissected and immersion-fixed in 4% paraformaldehyde (5 h, 24 h, 5 h, 3 h, 4 h, 8 h and 2 h, respectively) and were cryopreserved in 30% sucrose at 4°C. Tissue was embedded in TissueTek and cryosectioned (20 µm for small intestine and DRG; 40 µm for thyroid, bladder and spinal cord; 50 µm for brain and skin). Sections were either immunostained free-floating or thaw mounted onto SuperFrost Plus slides and stored at −20°C until needed.

Tissue was rehydrated in PBS, rinsed with TBST (0.05 M Tris, 2.7% NaCl, 0.3% Triton-X 100, pH 7.6), then blocked with 10% neat donkey serum (NDS) in TBST for 1 h at room temperature. Sections were incubated overnight at 4°C with primary antibodies. The following reagents were used: Isolectin Griffonia simplicifolia IB4, Alexa 568 conjugate (1[ratio]100, Invitrogen, I21412), chicken anti-GFP (1[ratio]600; Aves Labs, GFP-1020), rabbit anti-GFP (1[ratio]600; Invitrogen, A11122), rabbit anti-CGRP (1[ratio]750; Peninsula, T-4032), sheep anti-CGRP (1[ratio]250; Enzo Life Sciences, CA1137), mouse anti-NeuN (1[ratio]200; Millipore, MAB377), chicken anti-PAP (1[ratio]4,000; Aves Labs), rat anti-TRPM8 (1[ratio]100; a generous gift from Masatoshi Takeichi) [65], rabbit anti-PGP9.5 (1[ratio]500; Ultraclone), rabbit anti-NF200 (1[ratio]500; Sigma, N4142) and goat anti-HB-EGF (1[ratio]1,000; R&D Systems, AF-259-NA), which labels DTR. Tissue was rinsed and then blocked for 1 h in 10% NDS in TBST. Sections were incubated for 2 h in 10% NDS in TBST with Alexa fluor-conjugated secondary antibodies (Invitrogen). DRAQ5 (1[ratio]10; Cell Signaling, 4084) was used to label nuclei. PAP, TRPV1 and DTR immunostaining was performed using amplification, as described previously [66]. All fluorescent images were obtained using a Zeiss LSM 510 confocal microscope (Zeiss, Thornwood, NY).

For diaminobenzidine (DAB) staining, brain sections were processed as described above with chicken anti-GFP (1[ratio]5,000). On day 2, the sections were washed in TBST and then blocked for 30 min. Sections were incubated for 2 h in biotinylated donkey anti-chicken IgG (1[ratio]500), which was followed by washes in TBST. Sections were incubated with the Vectastain ABC complex in TBST for 2 h and washed. Sections were treated with a DAB solution (0.02% DAB, 0.01% H2O2 and 0.005% nickel ammonium sulfate in TBST) for 15 min. Following TBST washes and a PBS rinse, the sections were immersed in 0.2% gelatin in water, mounted onto Superfrost Plus slides and then air-dried for 4 days. Lastly, the sections were dehydrated with graded ethanols, cleared with xylene and coverslipped with DPX.

Supporting Information

Table S1

Percentage of CGRPα-GFP+/− DRG neurons of a given size class (small, medium, large diameter) that respond to the indicated agonists.


Table S2

Percentage of GFP-negative DRG neurons of a given size class (small, medium, large diameter) that respond to the indicated agonists.



We thank JrGang Cheng at the University of North Carolina (UNC) BAC Core for generating the CGRPα targeting arms, the UNC Animal Models Core for embryonic stem cell work and producing chimeras, Sarah Shoemaker for mouse colony management and small intestine immunohistochemistry, Brendan Fitzpatrick for technical support, Kenji Kohno for providing DTR (pTRECK1) plasmid and Masatoshi Takeichi for providing TRPM8 antibody.


Competing Interests: The authors have declared that no competing interests exist.

Funding: This work was supported by grants to MJZ from The Searle Scholars Program, The Klingenstein Foundation, The Rita Allen Foundation and NINDS (R01NS060725, R01NS067688). Confocal imaging was performed at the UNC Confocal and Multiphoton Imaging Core. The BAC Core and Imaging Core are funded by grants from NINDS (P30NS045892) and NICHD. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


1. Basbaum AI, Bautista DM, Scherrer G, Julius D. Cellular and molecular mechanisms of pain. Cell. 2009;139:267–284. [PMC free article] [PubMed]
2. Gold MS, Gebhart GF. Nociceptor sensitization in pain pathogenesis. Nat Med. 2010;16:1248–1257. [PubMed]
3. Zylka MJ, Sowa NA, Taylor-Blake B, Twomey MA, Herrala A, et al. Prostatic acid phosphatase is an ectonucleotidase and suppresses pain by generating adenosine. Neuron. 2008;60:111–122. [PMC free article] [PubMed]
4. Silverman JD, Kruger L. Selective neuronal glycoconjugate expression in sensory and autonomic ganglia: relation of lectin reactivity to peptide and enzyme markers. J Neurocytol. 1990;19:789–801. [PubMed]
5. Cavanaugh DJ, Lee H, Lo L, Shields SD, Zylka MJ, et al. Distinct subsets of unmyelinated primary sensory fibers mediate behavioral responses to noxious thermal and mechanical stimuli. Proc Natl Acad Sci U S A. 2009;106:9075–9080. [PubMed]
6. Rau KK, McIlwrath SL, Wang H, Lawson JJ, Jankowski MP, et al. Mrgprd enhances excitability in specific populations of cutaneous murine polymodal nociceptors. J Neurosci. 2009;29:8612–8619. [PMC free article] [PubMed]
7. Lawson SN, Crepps B, Perl ER. Calcitonin gene-related peptide immunoreactivity and afferent receptive properties of dorsal root ganglion neurones in guinea-pigs. J Physiol. 2002;540:989–1002. [PubMed]
8. McCarthy PW, Lawson SN. Cell type and conduction velocity of rat primary sensory neurons with calcitonin gene-related peptide-like immunoreactivity. Neuroscience. 1990;34:623–632. [PubMed]
9. Cavanaugh DJ, Chesler AT, Braz JM, Shah NM, Julius D, et al. Restriction of transient receptor potential vanilloid-1 to the peptidergic subset of primary afferent neurons follows its developmental downregulation in nonpeptidergic neurons. J Neurosci. 2011;31:10119–10127. [PMC free article] [PubMed]
10. Mishra SK, Hoon MA. Ablation of TrpV1 neurons reveals their selective role in thermal pain sensation. Mol Cell Neurosci. 2010;43:157–163. [PMC free article] [PubMed]
11. Karai L, Brown DC, Mannes AJ, Connelly ST, Brown J, et al. Deletion of vanilloid receptor 1-expressing primary afferent neurons for pain control. J Clin Invest. 2004;113:1344–1352. [PMC free article] [PubMed]
12. Imamachi N, Park GH, Lee H, Anderson DJ, Simon MI, et al. TRPV1-expressing primary afferents generate behavioral responses to pruritogens via multiple mechanisms. Proc Natl Acad Sci U S A. 2009;106:11330–11335. [PubMed]
13. Lawson JJ, McIlwrath SL, Woodbury CJ, Davis BM, Koerber HR. TRPV1 unlike TRPV2 is restricted to a subset of mechanically insensitive cutaneous nociceptors responding to heat. J Pain. 2008;9:298–308. [PMC free article] [PubMed]
14. Emeson RB, Hedjran F, Yeakley JM, Guise JW, Rosenfeld MG. Alternative production of calcitonin and CGRP mRNA is regulated at the calcitonin-specific splice acceptor. Nature. 1989;341:76–80. [PubMed]
15. Silverman JD, Kruger L. Calcitonin-gene-related-peptide-immunoreactive innervation of the rat head with emphasis on specialized sensory structures. J Comp Neurol. 1989;280:303–330. [PubMed]
16. Mulderry PK, Ghatei MA, Spokes RA, Jones PM, Pierson AM, et al. Differential expression of alpha-CGRP and beta-CGRP by primary sensory neurons and enteric autonomic neurons of the rat. Neuroscience. 1988;25:195–205. [PubMed]
17. Schutz B, Mauer D, Salmon AM, Changeux JP, Zimmer A. Analysis of the cellular expression pattern of beta-CGRP in alpha-CGRP-deficient mice. J Comp Neurol. 2004;476:32–43. [PubMed]
18. Rice FL, Albers KM, Davis BM, Silos-Santiago I, Wilkinson GA, et al. Differential dependency of unmyelinated and A delta epidermal and upper dermal innervation on neurotrophins, trk receptors, and p75LNGFR. Dev Biol. 1998;198:57–81. [PubMed]
19. Benemei S, Nicoletti P, Capone JG, De Cesaris F, Geppetti P. Migraine. Handb Exp Pharmacol. 2009:75–89. [PubMed]
20. Biella G, Panara C, Pecile A, Sotgiu ML. Facilitatory role of calcitonin gene-related peptide (CGRP) on excitation induced by substance P (SP) and noxious stimuli in rat spinal dorsal horn neurons. An iontophoretic study in vivo. Brain Res. 1991;559:352–356. [PubMed]
21. Saria A, Gamse R, Petermann J, Fischer JA, Theodorsson-Norheim E, et al. Simultaneous release of several tachykinins and calcitonin gene-related peptide from rat spinal cord slices. Neurosci Lett. 1986;63:310–314. [PubMed]
22. Mogil JS, Miermeister F, Seifert F, Strasburg K, Zimmermann K, et al. Variable sensitivity to noxious heat is mediated by differential expression of the CGRP gene. Proc Natl Acad Sci U S A. 2005;102:12938–12943. [PubMed]
23. Salmon AM, Damaj I, Sekine S, Picciotto MR, Marubio L, et al. Modulation of morphine analgesia in alphaCGRP mutant mice. Neuroreport. 1999;10:849–854. [PubMed]
24. Salmon AM, Damaj MI, Marubio LM, Epping-Jordan MP, Merlo-Pich E, et al. Altered neuroadaptation in opiate dependence and neurogenic inflammatory nociception in alpha CGRP-deficient mice. Nat Neurosci. 2001;4:357–358. [PubMed]
25. Zhang L, Hoff AO, Wimalawansa SJ, Cote GJ, Gagel RF, et al. Arthritic calcitonin/alpha calcitonin gene-related peptide knockout mice have reduced nociceptive hypersensitivity. Pain. 2001;89:265–273. [PubMed]
26. Zylka MJ, Rice FL, Anderson DJ. Topographically distinct epidermal nociceptive circuits revealed by axonal tracers targeted to Mrgprd. Neuron. 2005;45:17–25. [PubMed]
27. Caterina MJ, Schumacher MA, Tominaga M, Rosen TA, Levine JD, et al. The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature. 1997;389:816–824. [PubMed]
28. Xiao B, Dubin AE, Bursulaya B, Viswanath V, Jegla TJ, et al. Identification of transmembrane domain 5 as a critical molecular determinant of menthol sensitivity in mammalian TRPA1 channels. J Neurosci. 2008;28:9640–9651. [PMC free article] [PubMed]
29. Karashima Y, Damann N, Prenen J, Talavera K, Segal A, et al. Bimodal action of menthol on the transient receptor potential channel TRPA1. J Neurosci. 2007;27:9874–9884. [PubMed]
30. Wrigley PJ, Jeong HJ, Vaughan CW. Primary afferents with TRPM8 and TRPA1 profiles target distinct subpopulations of rat superficial dorsal horn neurones. Br J Pharmacol. 2009;157:371–380. [PMC free article] [PubMed]
31. Liu Q, Tang Z, Surdenikova L, Kim S, Patel KN, et al. Sensory neuron-specific GPCR Mrgprs are itch receptors mediating chloroquine-induced pruritus. Cell. 2009;139:1353–1365. [PMC free article] [PubMed]
32. Peier AM, Moqrich A, Hergarden AC, Reeve AJ, Andersson DA, et al. A TRP channel that senses cold stimuli and menthol. Cell. 2002;108:705–715. [PubMed]
33. McKemy DD, Neuhausser WM, Julius D. Identification of a cold receptor reveals a general role for TRP channels in thermosensation. Nature. 2002;416:52–58. [PubMed]
34. Zwick M, Davis BM, Woodbury CJ, Burkett JN, Koerber HR, et al. Glial cell line-derived neurotrophic factor is a survival factor for isolectin B4-positive, but not vanilloid receptor 1-positive, neurons in the mouse. J Neurosci. 2002;22:4057–4065. [PubMed]
35. Conrath M, Taquet H, Pohl M, Carayon A. Immunocytochemical evidence for calcitonin gene-related peptide-like neurons in the dorsal horn and lateral spinal nucleus of the rat cervical spinal cord. J Chem Neuroanat. 1989;2:335–347. [PubMed]
36. Tie-Jun SS, Xu Z, Hokfelt T. The expression of calcitonin gene-related peptide in dorsal horn neurons of the mouse lumbar spinal cord. Neuroreport. 2001;12:739–743. [PubMed]
37. Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, et al. Genome-wide atlas of gene expression in the adult mouse brain. Nature. 2007;445:168–176. [PubMed]
38. Neumann S, Braz JM, Skinner K, Llewellyn-Smith IJ, Basbaum AI. Innocuous, not noxious, input activates PKCgamma interneurons of the spinal dorsal horn via myelinated afferent fibers. J Neurosci. 2008;28:7936–7944. [PubMed]
39. Polgár E, Fowler JH, McGill MM, Todd AJ. The types of neuron which contain protein kinase C gamma in rat spinal cord. Brain Res. 1999;833:71–80. [PubMed]
40. Noguchi K, Senba E, Morita Y, Sato M, Tohyama M. Alpha-CGRP and beta-CGRP mRNAs are differentially regulated in the rat spinal cord and dorsal root ganglion. Brain Res Mol Brain Res. 1990;7:299–304. [PubMed]
41. Navarro X, Verdu E, Wendelscafer-Crabb G, Kennedy WR. Innervation of cutaneous structures in the mouse hind paw: a confocal microscopy immunohistochemical study. J Neurosci Res. 1995;41:111–120. [PubMed]
42. Kruger L, Silverman JD, Mantyh PW, Sternini C, Brecha NC. Peripheral patterns of calcitonin-gene-related peptide general somatic sensory innervation: cutaneous and deep terminations. J Comp Neurol. 1989;280:291–302. [PubMed]
43. Ishida-Yamamoto A, Senba E, Tohyama M. Distribution and fine structure of calcitonin gene-related peptide-like immunoreactive nerve fibers in the rat skin. Brain Res. 1989;491:93–101. [PubMed]
44. Tan LL, Bornstein JC, Anderson CR. Distinct chemical classes of medium-sized transient receptor potential channel vanilloid 1-immunoreactive dorsal root ganglion neurons innervate the adult mouse jejunum and colon. Neuroscience. 2008;156:334–343. [PubMed]
45. Ohtani R, Kaneko T, Kline LW, Labedz T, Tang Y, et al. Localization of calcitonin gene-related peptide in the small intestine of various vertebrate species. Cell Tissue Res. 1989;258:35–42. [PubMed]
46. Robine S, Huet C, Moll R, Sahuquillo-Merino C, Coudrier E, et al. Can villin be used to identify malignant and undifferentiated normal digestive epithelial cells? Proc Natl Acad Sci U S A. 1985;82:8488–8492. [PubMed]
47. Kawai Y, Takami K, Shiosaka S, Emson PC, Hillyard CJ, et al. Topographic localization of calcitonin gene-related peptide in the rat brain: an immunohistochemical analysis. Neuroscience. 1985;15:747–763. [PubMed]
48. Kresse A, Jacobowitz DM, Skofitsch G. Detailed mapping of CGRP mRNA expression in the rat central nervous system: comparison with previous immunocytochemical findings. Brain Res Bull. 1995;36:261–274. [PubMed]
49. Hokfelt T, Arvidsson U, Ceccatelli S, Cortes R, Cullheim S, et al. Calcitonin gene-related peptide in the brain, spinal cord, and some peripheral systems. Ann N Y Acad Sci. 1992;657:119–134. [PubMed]
50. Kruger L, Mantyh PW, Sternini C, Brecha NC, Mantyh CR. Calcitonin gene-related peptide (CGRP) in the rat central nervous system: patterns of immunoreactivity and receptor binding sites. Brain Res. 1988;463:223–244. [PubMed]
51. Gong S, Zheng C, Doughty ML, Losos K, Didkovsky N, et al. A gene expression atlas of the central nervous system based on bacterial artificial chromosomes. Nature. 2003;425:917–925. [PubMed]
52. Davidson S, Giesler GJ. The multiple pathways for itch and their interactions with pain. Trends Neurosci. 2010;33:550–558. [PMC free article] [PubMed]
53. Dhaka A, Earley TJ, Watson J, Patapoutian A. Visualizing cold spots: TRPM8-expressing sensory neurons and their projections. J Neurosci. 2008;28:566–575. [PubMed]
54. Takashima Y, Daniels RL, Knowlton W, Teng J, Liman ER, et al. Diversity in the neural circuitry of cold sensing revealed by genetic axonal labeling of transient receptor potential melastatin 8 neurons. J Neurosci. 2007;27:14147–14157. [PMC free article] [PubMed]
55. Baillie LD, Hagen V, Gardner KM, Mulligan SJ. Functional imaging within individual pain fibres ex vivo with optical microscopy. J Neurosci Methods. 2011;198:274–279. [PubMed]
56. Brown AG, Iggo A. A quantitative study of cutaneous receptors and afferent fibres in the cat and rabbit. J Physiol. 1967;193:707–733. [PubMed]
57. Woodbury CJ, Ritter AM, Koerber HR. Central anatomy of individual rapidly adapting low-threshold mechanoreceptors innervating the “hairy" skin of newborn mice: early maturation of hair follicle afferents. J Comp Neurol. 2001;436:304–323. [PubMed]
58. Saito M, Iwawaki T, Taya C, Yonekawa H, Noda M, et al. Diphtheria toxin receptor-mediated conditional and targeted cell ablation in transgenic mice. Nat Biotechnol. 2001;19:746–750. [PubMed]
59. Hasegawa H, Abbott S, Han BX, Qi Y, Wang F. Analyzing somatosensory axon projections with the sensory neuron-specific Advillin gene. J Neurosci. 2007;27:14404–14414. [PubMed]
60. Zurborg S, Piszczek A, Martinez C, Hublitz P, Al Banchaabouchi M, et al. Generation and characterization of an Advillin-Cre driver mouse line. Mol Pain. 2011;7:66. [PMC free article] [PubMed]
61. Stirling LC, Forlani G, Baker MD, Wood JN, Matthews EA, et al. Nociceptor-specific gene deletion using heterozygous NaV1.8-Cre recombinase mice. Pain. 2005;113:27–36. [PubMed]
62. Agarwal N, Offermanns S, Kuner R. Conditional gene deletion in primary nociceptive neurons of trigeminal ganglia and dorsal root ganglia. Genesis. 2004;38:122–129. [PubMed]
63. Campagnola L, Wang H, Zylka MJ. Fiber-coupled light-emitting diode for localized photostimulation of neurons expressing channelrhodopsin-2. J Neurosci Methods. 2008;169:27–33. [PubMed]
64. Wang H, Zylka MJ. Mrgprd-expressing polymodal nociceptive neurons innervate most known classes of substantia gelatinosa neurons. J Neurosci. 2009;29:13202–13209. [PMC free article] [PubMed]
65. Suzuki SC, Furue H, Koga K, Jiang N, Nohmi M, et al. Cadherin-8 is required for the first relay synapses to receive functional inputs from primary sensory afferents for cold sensation. J Neurosci. 2007;27:3466–3476. [PubMed]
66. Taylor-Blake B, Zylka MJ. Prostatic acid phosphatase is expressed in peptidergic and nonpeptidergic nociceptive neurons of mice and rats. PLoS One. 2010;5:e8674. [PMC free article] [PubMed]

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