Abstract
Timely initiation and termination of inflammatory response after corneal epithelial abrasion is critical for the recovery of vision. The cornea is innervated with rich sensory nerves with highly dense TRPV1 nociceptors. However, the roles of TRPV1+ sensory neurons in corneal inflammation after epithelial abrasion are not completely understood. Here, we found that depletion of TRPV1+ sensory nerves using resiniferatoxin (RTX) and blockade of TRPV1 using AMG-517 delayed corneal wound closure and enhanced the infiltration of neutrophils and γδ T cells to the wounded cornea after epithelial abrasion. Furthermore, depletion of TRPV1+ sensory nerves increased the number and TNF-α production of corneal CCR2+ macrophages and decreased the number of corneal CCR2– macrophages and IL-10 production. In addition, the TRPV1+ sensory nerves inhibited the recruitment of neutrophils and γδ T cells to the cornea via RAMP1 and SSTR5 signaling, decreased the responses of CCR2+ macrophages via RAMP1 signaling, and increased the responses of CCR2– macrophages via SSTR5 signaling. Collectively, our results suggest that the TRPV1+ sensory nerves suppress inflammation to support corneal wound healing via RAMP1 and SSTR5 signaling, revealing potential approaches for improving defective corneal wound healing in patients with sensory neuropathy.
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Introduction
The cornea, a transparent and avascular tissue in the anterior segment of the eyeball, provides almost 70% refraction of the optical axis1,2. Owing to external exposure, the cornea is susceptible to mechanical or chemical injury3,4. Modern laser refractive surgery further amplifies this problem5,6. The risk of microbial infections, keratohelcosis, and stromal turbidity increases if the wounded cornea does not completely heal in time7. Therefore, completely understanding the mechanisms of corneal wound healing and identifying more potential targets for the therapy of defective wound healing in the cornea are critical.
Healing of the injured cornea is a complicated process, which involves re-epithelialization, inflammation, and cell proliferation at the early stage and corneal stromal remodeling at the late stage1. Among these events, balanced inflammation is crucial for high-quality healing8,9,10,11,12,13. Immune cells involved in corneal wound repair play a distinct role in the wound healing process. After corneal injury, neutrophils are the first to migrate to the injured cornea from corneal limbal vessels as the first-line immune cells8. Infiltrating neutrophils clean the wound area by releasing enzymes and phagocytosing and promote the ingrowth of corneal nerves by releasing growth factors such as vascular endothelium growth factor9. Resident and infiltrating γδ T cells in the injured cornea recruit neutrophils to the inured cornea by producing IL-17A and directly stimulate the division and migration of corneal epithelial cells by producing IL-2214. Two different macrophage subsets (CCR2+ and CCR2–) stimulate inflammatory responses by releasing pro-inflammatory cytokines and inhibit the inflammatory response by producing immunosuppressive cytokines, respectively12. Infiltrating natural killer cells prevent the excessive accumulation and tissue-injuring activity of neutrophils after corneal injury11. The resident innate lymphoid type 2 cells in the corneal limbus promote corneal epithelial division and migration by producing amphiregulin, a type of epidermal growth factor15. Any event that disturbs the migration and activity of these immune cells affects the quality of corneal wound healing.
The cornea is densely innervated by three main functional classes of sensory neurons, broadly classified as polymodal nociceptors, pure mechano-nociceptors, and cold-sensing neurons16,17. After sensing different stimuli, such as mechanical, chemical, or thermal stimuli, these receptors initiate essential protective reflexes, such as increased blinking rate and tear secretion18,19. Thus, these sensory fibers play a crucial role in the maintenance of corneal homeostasis and the response to different stimulations. The transient receptor potential vanilloid 1 (TRPV1) positive nerve fibers comprise approximately 45% of the sensory nerves20. Recently, TRPV1 has been extensively studied for its use in the regulation of inflammation21,22,23,24. Activation of TRPV1+ sensory nerves can exert pro- and anti-inflammatory effects in vivo, depending on the type of neuropeptide released. For example, these nerve fibers have been shown to inhibit the recruitment of neutrophils and γδ T cells in bacterially infected lung tissue by secreting calcitonin gene-related peptide (CGRP)25 to increase IL-10 expression and reduce TNF-α expression in macrophages26,27. However, following lung injury, released substance P (SP) has been shown to stimulate IL-6, TNF-α, and MCP-1 production in lung epithelial cells28, while secreted SST suppresses the systemic immune responses29,30. In the Pseudomonas aeruginosa keratitis model, sensory nerves alter corneal inflammation progress through a CGRP-driven increase in neutrophil recruitment to the site of infection but inhibit its bactericidal activity31 and promote the transformation of macrophages from the M1 to M2 phenotype32. In the topical resiniferatoxin (RTX)-induced TRPV1+ sensory nerve denervation model33 and in the genetically TRPV1 deficient mouse model34, a significant delay in corneal wound repair was found. However, this delay was significantly reversed by topical application of neuropeptides CGRP, substance P (SP), and vasoactive intestinal peptide (VIP)33. Despite this knowledge, the underlying mechanisms of TRPV1 in mediating the post-traumatic corneal inflammatory response have not been well defined.
Considering the important role of the TRPV1+ sensory nerves in systemic and local inflammation, we hypothesized that TRPV1+ sensory nerves in the cornea might also play an important role in the corneal wound healing process. To address this issue, we investigated wound closure and inflammatory reaction after corneal abrasion in mice with RTX-mediated ablation of TRPV1+ sensory nerves and AMG-517-mediated pharmacological blockade of TRPV1. Furthermore, we analyzed the transcriptional profiles for neuropeptide receptors in neutrophils, γδ T cells, and macrophages, which are involved in inflammation in the wounded cornea. With topical administration of the agonists or antagonists for these neuropeptide receptors, we further validated the importance of the related signaling pathway in modulating inflammation after corneal epithelial abrasion. Overall, our findings reveal a previously unexpected, but critical, mechanistic role for TRPV1+ sensory nerves coordinating corneal inflammation after epithelial abrasion via neuropeptide receptors.
Results
Ablation of TRPV1+ sensory nerves impaired corneal wound closure
Immunostaining of cornea showed that corneal nerve terminal expressed TRPV1 (Fig. 1a). To determine the role of TRPV1+ sensory nerves in corneal wound healing, RTX was used to deplete TRPV1+ sensory nerves as described previously35,36. As expected, after subcutaneous injection with RTX for four weeks, both the expression of TRPV1 (Fig. 1b, d), the density of nerve fibers in the cornea (Fig. 1e, f, g) and the corneal sensitivity (Fig. 1h) decreased significantly. Compared with in vehicle˗treated animals, wound closure (Fig. 1i) and epithelial division (Fig. 1k, l) were significantly impaired following corneal abrasion in RTX˗treated animals. To investigate the alteration in the molecular signature between the RTX˗treated and vehicle˗treated corneas after corneal abrasion, the transcriptomic profiles were determined using RNA sequencing. The expression of genes involved in the metabolic process and the cell proliferation and migration decreased in RTX˗treated mice (Fig. 2a, b). Furthermore, Cytoscape network analysis of corneal gene transcription revealed that genes involved in epithelial cell proliferation and migration were mostly down-regulated, whereas those involved in the epithelial cell apoptosis were mostly up-regulated (Fig. 2c). Thus, the changes in corneal gene transcription indicated that RTX treatment delayed corneal wound healing.
Ablation of TRPV1+ sensory nerves increased inflammation after epithelial abrasion
To determine the influence of TRPV1+ sensory nerves on corneal inflammation after epithelial abrasion, we first analyzed the alteration in corneal genes involved in immune response. Data showed that the expression of genes involved in immunity and chemotaxis, especially those of Il6, Tnf, Cxcr1, and Cxcr2, increased in the corneas of RTX-treated mice (Fig. 3a). Cytoscape network analysis revealed that genes involved in the neutrophil chemotaxis, migration, activation, degranulation, mediated cytotoxicity, and the γδ T cell activation and differentiation were mostly up-regulated (Fig. 3b). Next, we investigated the influx of neutrophils and γδ T cells in the injured cornea. Immunostaining of the cornea showed that the number of infiltrating neutrophils within the region of the corneal wound margin at 6, 12, 18, 24, 30, and 36 h after epithelial abrasion and that of infiltrating γδ T cells at 24, 30, and 36 h after epithelial abrasion in RTX˗treated mice were significantly higher than those in vehicle˗treated mice (Fig. 3d, e). Flow cytometric analysis at 18 h after corneal abrasion further showed that ablation of TRPV1+ sensory nerves exacerbated corneal inflammation after corneal injury (Fig. 3g). These data suggest that RTX treatment exacerbated corneal inflammation after epithelial abrasion.
Blockade of TRPV1 function impaired corneal wound closure and exaggerated inflammation after epithelial abrasion
To further confirm the specific roles of TRPV1+ sensory nerves in modulating corneal wound healing and inflammation after epithelial abrasion, we topically applied AMG-517, a TRPV1 antagonist37,38, and inhibited the function of TRPV1+ sensory nerves. Consistent with the results of our previous studies, the wound in control mice closed 24 h after epithelial abrasion. However, corneal wounds in AMG-517-treated mice did not close until 30 h after epithelial abrasion (Fig. 4a). Similarly, the number of dividing epithelial cells in AMG-517-treated corneas was significantly lower than in vehicle-treated corneas (Fig. 4b). To evaluate the effects of blockade of TRPV1 function on injury-induced inflammation after abrasion, the number of infiltrating neutrophils and γδ T cells in the cornea was enumerated in vehicle-treated and AMG-517-treated corneas. After treatment with AMG-517, the number of neutrophils within the region of the corneal wound margin and γδ T cells within the perilimbal region significantly increased at 12, 18, 24, and 30 h after epithelial abrasion (Fig. 4c). In addition, flow cytometric analysis further confirmed that the number of neutrophils and γδ T cells in AMG-517-treated cornea was more than in the cornea of vehicle-treated mice at 18 h after epithelial abrasion (Fig. 4d).
TRPV1+ sensory nerves suppressed the recruitment of neutrophils and γδ T cells via RAMP1 and SSTR5 signals
Sensory nerves modulate the responses of immune cells, usually by releasing neuropeptides23,24. Immunostaining of cornea showed that nerve fibers expressed CGRP and SST (Fig. 5a). To determine whether the RTX-mediated ablation of TRPV1+ sensory nerves affected the production of neuropeptides in the cornea, we compared the gene expression of neuropeptides in corneal cells using quantitative polymerase chain reaction (qPCR) analysis, as mRNA localization and local protein synthesis in axons have been reported previously39,40. Both Cgrp and Sst levels decreased after RTX treatment 12 h post-epithelial abrasion (Fig. 5b). Neutrophils in the cornea expressed the CGRP receptor gene, Ramp1, and the SST receptor genes, Sstr1-5. Among these, Sstr5 was predominately expressed in neutrophils. However, the γδ T cells in the cornea expressed Ramp1 and Sstr5 (Fig. 5c). This suggests that the increase in the recruitment of neutrophils and γδ T cells to the RTX˗treated cornea may be due to the decrease in the activity of RAMP1-CGRP or SST-SSTR5 signaling in the cornea. To confirm this hypothesis, we first block the function of RAMP1 and SSTR5 and observed the alteration of neutrophils and γδ T cells. When the injured corneas of normal mice were topically treated with BIBN 4096, the RAMP1 antagonist, and BIM 23056, the SSTR5 antagonist, the number of both neutrophils and γδ T cells in the cornea increased (Fig. 5d, e). Second, eyedrops of CGRP or L˗817818, an SSTR5 agonist, were administered to the eyes of the RTX˗treated mice. The results showed that the number of neutrophils and γδ T cells (Fig. 5f, g), the expression of Il1β and Il18 in neutrophils (Fig. 5h), and the expression of Il17a and Tnfα in γδ T cells (Fig. 5i) in the cornea of RTX˗treated mice decreased after treatment with CGRP or L˗817818. Thus, these results revealed that the TRPV1+ sensory nerves inhibited the infiltration of neutrophils and γδ T cells to the cornea and the expression of pro-inflammatory cytokines in neutrophils and γδ T cells via RAMP1 and SSTR5 signaling.
TRPV1+ sensory nerves regulated the responses of CCR2– and CCR2+ corneal macrophages after epithelial abrasion via RAMP1 and SSTR5 signals
Macrophages modulate various types of inflammatory response and are controlled by sensory nerves41,42. Hence, we speculated that corneal macrophages may be regulated by TRPV1+ sensory nerves during corneal wound healing. Our previous study showed that corneal macrophages can be classified into CCR2+ and CCR2– subsets. The CCR2+ macrophages (M1 subtype) promoted inflammation in the injured cornea with secretion of TNF˗α and IL˗1β, whereas the CCR2– macrophages (M2 subtype) inhibited inflammation with the secretion of IL˗1012. In this study, Cytoscape network analysis of corneal gene transcription showed that genes involved in monocyte chemotaxis and macrophage differentiation in RTX-treated-corneas were mostly up-regulated. In the gene set related to macrophage activation, we found that the expression of M1 macrophage-related genes (Cd86, Cd80, Fpr2, and Tnf)43,44,45 increased, whereas the expression of M2 macrophage-related genes (Cxcl13, Sucnr1, Cd163, and Retnla)45,46,47,48 decreased (Fig. 6a). Flow cytometric analysis showed that in the cornea of RTX˗treated mice, the number of CCR2+ macrophages increased, and that of CCR2– macrophages decreased at 21 h after epithelial abrasion (Fig. 6e). In addition, the production of TNF˗α in CCR2+ macrophages increased, and that of IL˗10 in CCR2– macrophages decreased after RTX treatment 21 h post-epithelial abrasion (Fig. 6f). Using flow cytometric sorting and qPCR analysis, we found that corneal CCR2+ and CCR2– macrophages expressed Ramp1 and Sstr1–5. Among these, Ramp1 was predominantly expressed in CCR2+ macrophages, and Sstr5 in CCR2– macrophages (Fig. 6g). To investigate the roles of RAMP1 and SSTR5 in regulating the responses of corneal macrophages, we treated injured corneas of normal mice with drops of BIBN 4096, a RAMP1 antagonist, or BIM 23056, an SSTR5 antagonist. The number of CCR2+ macrophages increased, whereas that of the CCR2– macrophages did not change considerably after BIBN 4096 treatment (Fig. 6h). In contrast, the number of CCR2– macrophages decreased, whereas that of CCR2+ macrophages did not change significantly after BIM 23056 treatment (Fig. 6i). In addition, the production of TNF˗α in CCR2+ macrophages increased after BIBN 4096 treatment and that of IL˗10 in CCR2– macrophages decreased after BIM 23056 treatment (Fig. 6j). Furthermore, the number of CCR2+ macrophages in the cornea and the production of TNF˗α in these cells from RTX˗treated mice decreased after using CGRP locally (Fig. 6k). The number of CCR2– macrophages in the cornea and the amount of IL˗10 produced by these cells from RTX˗treated mice can be increased with local application of L˗817818 (Fig. 6l). Therefore, TRPV1+ sensory nerves suppress the response of CCR2+ macrophages via RAMP1 signaling and promote the response of CCR2– macrophages via SSTR5 signaling in the cornea.
CGRP and L-817,818 promoted corneal wound healing in RTX-treated mice
Both CGRP and L˗817,818 can decrease the inflammation after RTX-mediated depletion of TRPV1+ sensory nerves. To investigate whether CGRP and L˗817,818 promoted the healing of injured corneas in RTX˗treated mice, drops of CGRP and L˗817,818 were individually administered to these mice. The wound size of corneas in RTX˗treated mice decreased after treatment with CGRP (Fig. 7a) or L˗817,818 (Fig. 7c) 12, 18, and 24 h after epithelial abrasion. The number of dividing epithelial cells in RTX˗treated mice significantly increased after treatment with CGRP (Fig. 7b) or L˗817,818 (Fig. 7d) 18 h after epithelial abrasion. This indicated that activation of RAMP1 and SSTR5 can reverse the effect of RTX on corneal wound healing.
Discussion
In this study, we confirmed that the TRPV1+ sensory nerves are closely involved in the wound repair process of the cornea by balancing the inflammatory response, mainly via the RAMP1 and SSTR5 signals. We observed that (1) both ablation of TRPV1+ sensory nerves and blockade of TRPV1 increased inflammation in the cornea after epithelial abrasion; (2) activation of both RAMP1 and SSTR5 reduced the accumulation and pro-inflammatory cytokine expression of neutrophils and γδ T cells in the cornea of TRPV1+ sensory nerve˗ablated mice; (3) activation of RAMP1 reduced the CCR2+ macrophage distribution in the cornea and TNF˗α expression, whereas activation of SSTR5 increased the CCR2– macrophage distribution in the cornea and IL˗10 expression. These events act together to limit the excessive inflammatory response after corneal injury and promote the wound repair process in the cornea. Finally, we confirmed that topical administration of both CGRP and SSTR5 agonists improved the impaired corneal wound healing in the TRPV1+ sensory nerve˗ablated mice. The data obtained in this study further support the uniqueness of the cornea as an immune-privileged tissue and its corresponding mechanisms.
TRPV1+ sensory nerves in the cornea play a key role in maintaining corneal homeostasis and responding to different external stimuli16,17,18,19. In the present study, a comparative analysis of the corneal wound repair process and transcriptome after chemical TRPV1+ sensory nerve ablation and pharmacological intervention in TRPV1 signaling confirmed that the presence of TRPV1+ sensory nerves coordinated the re-epithelialization process after corneal epithelial abrasion, including epithelial division and migration. These results are consistent with previous findings in the corneas of TRPV1 genetically deficient and chemically TRPV1-ablated mice33,34. Similarly, the present study also found that chemical ablation of TRPV1+ nerves or pharmacological blockade of the TRPV1 signaling pathway significantly affected the extent of the inflammatory response following corneal injury, mainly in the form of increased recruitment of inflammatory cells (neutrophils, γδ T cells and CCR2+ macrophages) to the injured cornea and the expression of pro-inflammatory cytokine transcripts in the cornea. This is coherent with findings from other barrier site models of inflammation, such as pulmonary and cutaneous S. aureus infection25,49. Overall, these results suggest that TRPV1+ sensory nerves in the cornea play an important regulatory role, both qualitative and quantitative, in wound repair after corneal abrasions. Therefore, it is important to further explore the underlying molecular mechanisms, particularly in the inflammatory response.
Neutrophils are the first line of inflammatory cells recruited to the wounded cornea after corneal injury8,50,51. These cells contribute to its repair process by producing certain growth factors, such as VEGF, besides their role in killing contaminating microbes and cleaning the wound through the secretion of certain enzymes8,50,52. To explore the underlying mechanisms by which TRPV1+ nerves regulate neutrophil migration and function following corneal wounding, we first demonstrated that neutrophils trafficking to the injured cornea express the receptor SSTR5 corresponding to the neuropeptide SST. Second, topical administration of SSTR5 agonists reversed the increase in neutrophil infiltration induced by TRPV1+ nerve ablation of the cornea. However, neutrophil recruitment to the site of infection in both pulmonary and cutaneous models of infection is mainly via sensory neuropeptide CGRP receptor RAMP1-mediated signaling25,49 The reason for this discrepancy may be due to differences in the type, origin, and function of sensory nerve fibers at different barrier sites53,54,55 or different local microenvironments56,57.
Several studies have shown a close association between TRPV1+ neurons and γδ T cells at the barrier site25,54,58,59,60. When skin TRPV1+ neurons are stimulated by the TLR7 agonist imiquimod, they promote IL-23 production by dermal dendritic cells, which in turn stimulates dermal γδ T cells to secrete IL-17A, IL-17F, and IL-22, ultimately leading to the recruitment of more neutrophils to the skin and excessive keratinocyte proliferation58,59. Further studies have shown that cutaneous TRPV1+ neurons are activated by Candida albicans-derived β-glucan to suppress Candida albicans infection by releasing CGRP to drive IL-23 production by dendritic cells to promote IL-17 production by cutaneous γδ T cells, thereby activating downstream pathways60. However, mouse models from lethal S. aureus pneumonia found that TRPV1+ neurons down-regulated lung γδ T cells, leading to reduced recruitment of neutrophils, which are critical for bacterial clearance25. Removal of TRPV1+ neuroreceptors by RTX in mice increased the number of γδ T cells in the lung and significantly improved their survival25. γδ T cells are also abundant on the ocular surface and play an important regulatory role in maintaining ocular surface homeostasis and in response to foreign stimuli61. Following corneal injury, γδ T cells that reside and emigrate into the injured cornea attract neutrophils and platelets, primarily through the production of IL-17A9,14,62. Both neutrophils and platelets have the potential to promote corneal nerve growth through the release of growth factors, such as VEGF9,14,62. This study explored the interaction between TRPV1 and γδ T cells in a corneal abrasion model through three parallel experiments. First, we found that γδ T cells recruited to the traumatized cornea continuously expressed the neuropeptide CGRP receptor RAMP1 and the SST receptor SSTR5. Second, injured corneas in mice following RTX removal of TRPV1+ sensory nerves increased not only the number of locally recruited γδ T cells but also their expression of the pro-inflammatory cytokines Tnfα and Il17a. Consistent with this, local application of either CGRP or the SSTR5 agonist L-817,818 significantly reduced the number of γδ T cells recruited to injured corneas and their expression of the pro-inflammatory cytokines Tnf and Il17a in TRPV1+ sensory nerve-ablated mice. Thus, consistent with the findings in the lungs25, corneal stimulation of activated TRPV1+ sensory nerves modulate the inflammatory response process after corneal trauma by altering the migration of γδ T cells and their cytokine expression through the release of the neuropeptides CGRP and SST.
Our previous study indicated that the balance between CCR2– and CCR2+ macrophages regulated corneal inflammation via the autonomic nervous system during corneal wound healing12,63. Recent studies demonstrated that the macrophage reaction to different stimuli is also modulated by sensory nerve fibers via nociceptor-neuropeptide-macrophage interactions64. For instance, SP from sensory nerve fibers increased the number of M2 macrophages in arthritis65. CGRP up-regulated the expression of IL-10 in macrophages via cAMP/PKA signaling66,67,68, whereas it inhibited the expression of TNF-α in the peritoneal macrophages69. Vasoactive intestinal peptide (VIP) decreased the expression of TNF-α and IL-6 in macrophages via cAMP-dependent signaling70,71. The neuropeptide TAFA4 released by the activation of Gαi-interacting protein+ sensory neurons depresses the ultraviolet-induced skin inflammatory responses by promotion of embryonically derived TIM4+ macrophages to produce IL-1072. Similarly, our data showed that TRPV1+ nerve ablation with RTX significantly decreased the number of CCR2– macrophages and their expression of IL-10, whereas it increased the number of CCR2+ macrophages and their expression of TNF-α. Further analysis confirmed that corneal CCR2+ macrophages predominantly expressed the CGRP receptor Ramp1, whereas corneal CCR2– macrophages predominantly expressed Sstr5. Additionally, by topical administration of both agonist and antagonist for RAMP1 and SSTR5, respectively, we confirmed that the TRPV1+ sensory nerves inhibited the CCR2+ macrophage recruitment and TNF expression in the cornea via CGRP-RAMP1 signaling and promoted the production of IL-10 by CCR2– macrophages to dampen inflammation via SST-SSTR5 signaling. Thus, the integrated regulation of corneal macrophage responses by TRPV1+ sensory nerves suppresses the inflammatory response after corneal injury.
Of note, other resident or infiltrating immune cells, such as natural killer cells11, type 2 innate lymphoid cells (ILC2s)15, dendritic cells73,74, and mast cells75,76,77, also coordinate the corneal wound healing process through unique functions and mechanisms. These cells also co-localize with TRPV1+ sensory nerves and may express neuropeptide receptors for CGRP and SST. However, this study focused only on two subsets of macrophages, neutrophils, and γδ-T cells. Thus, the role of TRPV1+ sensory nerves affecting other types of immune cells through the above neuropeptide receptors in coordinating the whole process of wound repair needs to be further clarified. In addition, TRPV1+ sensory nerves also directly act on immune cells expressing corresponding receptors by releasing other neuropeptide mediators. Moreover, the TRPV1+ sensory nerve plays a different regulatory role by releasing other neuropeptides directly binding to corresponding receptors expressed on immune cells. Studies have shown that SP from TRPV1+ sensory nerves leads to degranulation of mast cells and the release of histamine and other cytokines by binding to Mas-related G protein-coupled receptor member B2 on mast cells78, whereas VIP activates ILC2s79 and type 2 T helper (Th2) cells through the VPAC2 receptor80. Finally, inflammatory mediators and even neuropeptides released from activated immune cells might sensitize TRPV1+ sensory nerve fibers via a feedback way using gating of ion channels23,81. Therefore, the crosstalk between all these factors still needs to be explored spatially and temporally by more research.
Collectively, our results confirmed that TRPV1+ sensory nerves suppressed corneal inflammation and promoted re˗epithelialization after epithelial abrasion by inhibiting neutrophil and γδ T cell infiltration, inhibiting CCR2+ macrophage response, and promoting CCR2– macrophage response via the RAMP1 and SSTR5 signaling pathways (Fig. 8). It is well known that corneal nerve density and corneal sensitivity are low in patients with diabetes. The corneas of these patients always show delayed wound healing and enhanced inflammation after injury. Our observations regarding the roles of TRPV1+ sensory nerves in modulating corneal inflammation via RAMP1 and SSTR5 signaling may reveal potential targets for improving corneal wound healing in diabetics.
Materials and methods
Animals
C57BL/6 J mice without any eye diseases were purchased from the Medical Experimental Animal Center (Foshan, Guangdong, China). Animals were maintained in a 12 h light/12 h dark cycle and fed a standard laboratory diet and water ad libitum. All animal protocols in this study were approved by the Jinan University Laboratory Animal Committee on Animal Welfare. All animals were treated in accordance with the Association for Research in Vision and Ophthalmology Statement for the Use of Animals in Ophthalmic and Vision Research. The animals were anesthetized via inhalation of 2% isoflurane and euthanized using an overdose of CO2 and cervical dislocation.
Depletion of TRPV1+ sensory nerves
RTX, a specific high-affinity agonist of TRPV1, was used to deplete TRPV1+ sensory nerves as described previously35,36. Female C57BL/6 mice aged four weeks were subcutaneously injected thrice with RTX (Tocris Bioscience, USA; no. 1137), and the dosage was increased over three consecutive days (30 μg/kg, 70 μg/kg, 100 μg/kg). To evaluate the effect of sensory nerve depletion, TRPV1 expression, corneal nerve density and sensitivity were measured 4 weeks after RTX treatment.
Corneal nerve imaging and density measurement
Corneal nerve imaging and density measurement were performed as described previously9,82,83. Briefly, the cornea with complete limbus was in situ removed from euthanized animals, fixed in 2% formaldehyde, washed with phosphate buffered saline (PBS), permeabilized with 0.1% Triton X˗100, blocked in 2% bovine serum albumin (BSA) in PBS, and incubated with neuron-specific beta˗III tubulin Alexa Fluor 488˗conjugated antibody (Sigma˗Aldrich, USA; no. AB15708A4). Images of each corneal zone were captured using a DeltaVision Elite high-resolution microscope imaging system (GE Healthcare, USA) under a 40× objective. The length of the corneal nerve fibers was analyzed using the Imaris software (Bitplane, Switzerland). Briefly, the image of corneal nerve fibers was loaded into the Imaris software. β˗III˗tubulin˗positive nerve fibers were detected, and their total length was calculated automatically. The nerve branch number or nerve length within 40× objective field of view of each corneal zone were represented as the relative nerve density of the specified corneal region.
Measurement of corneal sensitivity
Corneal sensitivity was analyzed using a Cochet-Bonnet esthesiometer (Luneau SAS, France; no. 8630-1490-29), as published previously83,84. Briefly, at different time points after epithelial abrasion, unanesthetized mice were held by the scruff of the neck and presented with a monofilament at lengths ranging from 6.0 to 0.5 cm in 0.5 cm increments to elicit a blink response. At each length, the monofilament touched the cornea four times, making perpendicular contact with the surface before considering a response to be negative (no blink response). The lack of a blink reflex at a monofilament length of 0.5 cm was recorded as “0.” All the measurements were performed by the same examiner, who was blinded to the animal groups.
Corneal wound healing model
Mouse corneas were mechanically abraded as described previously8,9,10,11,12,13. Briefly, the animals were anesthetized using an intraperitoneal injection of sodium phenobarbital (25–50 mg/kg). The central corneal epithelium was marked with a 2 mm trephine, and this labeled region was removed using a golf club spud (Accutome, Malvern, PA, USA).
Pharmacological agonism and antagonism
AMG-517 was used to block the function of TRPV1. Mouse eyes were pretreated for three days with AMG-517 (3 μl, 1 μg/μl; Selleck, USA; no. 659730-32-2) (three times each day) before corneal epithelial abrasion. Subsequently, the same concentration of AMG-517 was administered to the eyes after corneal epithelial abrasion every 6 h. To determine the roles of the CGRP receptor (RAMP1) and SSTR5 in modulating the recruitment of neutrophils and γδ T cells, as well as the responses of corneal CCR2– and CCR2+ macrophages, CGRP (3 μl, 0.5 μg/μl; R&D Systems; no. 1161) or the agonist of SSTR5, L˗817,818 (3 μl, 0.25 μg/μl; R&D Systems; no. 1980), was administered to the eyes of RTX-treated mice at −6, 0, 6, 12, 18, and 24 h after corneal epithelial abrasion. The antagonist of RAMP1, BIBN 4096 (3 μl, 2 μg/μl; Tocris Bioscience, USA; no. 4561), or the antagonist of SSTR5, BIM 23056 (3 μl, 2 μg/μl; R&D Systems; no. 1844), was administered to the eyes of normal mice at −6, 0, 6, 12, 18, and 24 h after corneal epithelial abrasion.
Immunostaining
The procedure was performed as described previously8,9,10,11,12,13. In brief, mouse eyes were fixed in 2% formaldehyde solution for one hour and dissected with corneal scissors under the dissecting microscope to obtain corneas with complete limbi. Corneas were washed thrice in PBS, blocked in 2% BSA for 15 min, and permeabilized in 0.1% Triton˗X 100 for 15 min. Next, corneal tissues were incubated overnight with anti˗β˗III tubulin antibody conjugated with Alexa Fluor 488 (1:100; Sigma˗Aldrich; no. AB15708A4), anti˗mouse TRPV1 antibody (1:100; ABclonal; no. A8564), anti˗mouse CGRP antibody (1:100; ABclonal; no. A5542), anti˗mouse SST antibody (1:100; ABclonal; no. A20617), anti˗mouse Ly6G antibody conjugated with fluorescein isothiocyanate (FITC) (1:100; BD Biosciences, USA; no. 551460), or anti˗mouse GL3 antibody conjugated with phycoerythrin (PE) (1:100; BD Biosciences; no. 553178) at 4 °C. Corneas incubated with anti-TRPV1/CGRP/SST antibodies were washed three times with PBS and then incubated with Alexa Fluor 594-conjugated secondary antibody anti-rabbit IgG (1:100; ABclonal; No. AS039) at 4 °C overnight. Then, the corneas were washed thrice in PBS, placed on a glass slide, and cut radially in four directions with surgical blades while flattening them. A fluorescent mounting medium containing 1 μM 4′,6˗diamidino˗2-phenylindole (DAPI) (Sigma˗Aldrich, USA; no. 28718˗90˗3) was placed on the corneas. Images of the corneas were analyzed using the DeltaVision microscopy imaging system (Applied Precision, Issaquah, WA, USA).
RNA sequencing
RNA sequencing from corneal bulk RNA was carried out as previously described85,86. In brief, total corneal RNA purity and concentration were determined. After RNA integrity was verified, construction and sequencing of the cDNA library were performed by the Beijing Genomics Institute (BGI) using the BGISEQ-500 platform. Each sample produced more than 20 M clean reads, which were mapped to the mm10 reference genome version using Spliced Transcripts Alignment to a Reference (STAR2.5.3a).
Flow cytometric analysis
Corneas with complete limbi were cut into pieces and digested in 4 mg/ml collagenase I (Sigma˗Aldrich, no. C0130) for 30 min. The digested suspension of corneal tissues was washed twice in PBS and passed through a 75 μm filter to obtain single cells. Then, corneal cells were blocked using flow cytometry staining buffer (eBioscience, USA; no. 00˗4222˗57) containing anti˗mouse CD16/32 antibody at room temperature for 10 min. To analyze neutrophils and γδ T cells, corneal cells were incubated with the following antibodies (1:100): anti˗mouse CD45 antibody conjugated with allophycocyanin (APC) (BD Biosciences; no. 559864), anti˗mouse CD11b antibody conjugated with Percp Cy5.5 (BD Biosciences; no. 550993), anti˗mouse Ly6G antibody conjugated with FITC (BD Biosciences; no. 551460), and anti˗mouse GL3 antibody conjugated with PE (BD Biosciences; no. 553178) at room temperature for 30 min. To analyze macrophages, corneal cells were incubated with the following antibodies (1:100): anti˗mouse CD45 antibody conjugated with FITC (BD Biosciences; no. 553080), anti˗mouse CD64 antibody conjugated with Brilliant violet 421 (Biolegend, USA; no. 139309), and anti˗mouse CCR2 antibody conjugated with PE (R&D Systems; no. FAB5538P) at room temperature for 30 min. To detect the production of TNF˗α and IL˗10 by the macrophages, the above stained corneal cells were fixed in 4% paraformaldehyde for 40 min and permeabilized in 0.01% Triton X˗100 for 8 min. These cells were washed in PBS and incubated with anti˗mouse TNF˗α antibody conjugated with APC (1:100; Biolegend; no. 506308) or IL˗10 antibody conjugated with APC (1:100; Biolegend; no. 505010) at room temperature for 30 min. Finally, these stained corneal cells were analyzed using BD FACSCanto.
Transcript amplification from neutrophils, γδ T cells, and corneal macrophages
Single corneal cells were incubated with the following antibodies: anti˗mouse CD45 antibody conjugated with APC, anti˗mouse CD11b antibody conjugated with Percp Cy5.5, anti˗mouse Ly6G antibody conjugated with FITC, and anti˗mouse GL3 antibody conjugated with PE, or anti˗mouse CD45 antibody conjugated with FITC, anti-mouse CD64 antibody conjugated with Brilliant violet 421, and anti˗mouse CCR2 antibody conjugated with PE at room temperature for 30 min. After washing with PBS, these cells were analyzed using the BD FACSAria to obtain CD45+CD11b+Ly6G+ neutrophils, CD45+CD11b─GL3+ γδ T cells, and CD45+CD64+CCR2– and CD45+CD64+CCR2+ macrophages. The mRNA of the sorted neutrophils, γδ T cells, and CCR2─ or CCR2+ macrophages was amplified and converted into DNA using a REPLI˗gWTA single cell kit (Qiagen, no. 150063).
qPCR
Corneas with complete limbi were placed in buffer RZ (Tiangen; no. RK145) and smashed using a TissueRuptor (Qiagen, Germantown, MD). The total RNA of corneal tissues was extracted using the RNAsimple total RNA kit (Tiangen; no. DP419). cDNA was obtained from total RNA of corneal tissues using a ReverTra Ace qPCR RT kit (Toyobo, Japan; no. FSQ˗101). The expression of target genes in corneal cDNA or amplified DNA of neutrophils, γδ T cells, and macrophages were analyzed using the THUNDERBIRD SYBR qPCR mix (Toyobo; no. QPS˗201). The primers used in this study are shown in the Table 1.
Statistical analysis
Data are presented as mean ± standard deviation (SD). For comparisons between groups, one˗way analysis of variance was performed. Statistical significance was set at P < 0.05.
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Acknowledgements
This work was supported by the National Natural Science Foundation of China through Grants 82171014 (to Z.L.), 32100715 (to J.L.), and 81770962 (to Z.L.), the Science and Technology Program of Guangzhou of China through Grant 202102020002 (to J.L.), and the PhD Start-up Fund of the Natural Science Foundation of Guangdong Province of China through Grant 2018A030310605 (to J.L.).
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Z.L. and J.L. conceived and designed the study. S.H. analyzed immunostaining and performed qPCR. R.Y., X.C., F.L., X.S., and P.X. helped with treatment of the animals, including the establishment of corneal injured model and drug treatment. J.L. performed flow cytometry analysis. Y.H., Y.X., and T.F. conducted the statistical analysis. J.L. drafted the first version of the paper. Z.L. critically reviewed and revised the paper for intellectual content. All authors critiqued the manuscript and approved its submission.
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Liu, J., Huang, S., Yu, R. et al. TRPV1+ sensory nerves modulate corneal inflammation after epithelial abrasion via RAMP1 and SSTR5 signaling. Mucosal Immunol 15, 867–881 (2022). https://doi.org/10.1038/s41385-022-00533-8
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DOI: https://doi.org/10.1038/s41385-022-00533-8