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Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system in which histamine (HA) and its receptors have been implicated in disease pathogenesis. HA exerts its effects through four different G protein-coupled receptors designated H1–H4. We previously examined the effects of traditional single HA receptor (HR) knockouts (KOs) in experimental allergic encephalomyelitis (EAE), the autoimmune model of MS. Our results revealed that H1R and H2R are propathogenic, while H3R and H4R are antipathogenic. This suggests that combinatorial targeting of HRs may be an effective disease-modifying therapy (DMT) in MS. To test this hypothesis, we generated H1H2RKO and H3H4RKO mice and studied them for susceptibility to EAE. Compared with wild-type (WT) mice, H1H2RKO mice developed a less severe clinical disease course, whereas the disease course of H3H4RKO mice was more severe. H1H2RKO mice also developed less neuropathology and disrupted blood brain barrier permeability compared with WT and H3H4RKO mice. Additionally, splenocytes from immunized H1H2RKO mice produced less interferon(IFN)-γ and interleukin(IL)-17. These findings support the concept that combined pharmacological targeting of HRs may be an appropriate ancillary DMT in MS and other immunopathologic diseases.
Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system (CNS) characterized by focal demyelination, axonal loss, and gliosis . Although the etiology of MS remains ill-defined, susceptibility likely results from a combination of factors, including genetic/epigenetic, environmental, immunological, hormonal, and infectious agents. Experimental allergic encephalomyelitis (EAE) is the autoimmune model of MS, in which disease pathogenesis is associated with major histocompatibility complex (MHC) class II-restricted CD4+T cells capable of secreting either interferon(IFN)-γ (Th1) or interleukin(IL)-17 (Th17) .
Histamine (HA, 2-(4-imidazole) ethylamine) is a biogenic monoamine that mediates a variety of physiological processes including neurotransmission, gastrointestinal and circulatory functions, secretion of pituitary hormones, cell proliferation, and hematopoiesis . In addition, HA is a potent mediator of inflammation and regulator of innate and adaptive immune responses . HA is synthesized by decarboxylation of L-histidine by the rate-limiting enzyme histidine decarboxylase (HDC). Mast cells and basophils are the major sources of stored HA in the body . However, induced or nascent secretion of HA can occur in other cell types including dendritic cells, T cells, neutrophils, macrophages, and immature myeloid cells [6–13]. HA exerts its effects by binding to four different G protein-coupled receptors designated H1–H4. H1R and H2R couple to second messenger signaling pathways via stimulatory G proteins (Gαq/11 and Gs, respectively), whereas H3R and H4R couple via inhibitory G proteins (Gi/o) [14–16]. HA has a diverse effect on many cell types due to differential expression of HRs and signaling through distinct intracellular signaling pathways. H1R and H2R are expressed more widely, while H4R expression is mostly restricted to hematopoietically derived cells. Recently, it has been shown that H4R is also expressed functionally in the CNS . H3R is primarily expressed within the CNS presynaptically, where it is an inhibitory auto- and heteroreceptor .
The role of HA in the pathogenesis of MS and EAE has been well documented . HA and agents causing its release from mast cells alter the permeability of the blood brain barrier (BBB) [20, 21]. The use of first-generation antihistamines, which can readily cross the BBB, is associated with a decrease in MS risk . Patients with relapsing-remitting or relapsing-progressive MS given the H1R antagonist hydroxyzine were reported to remain stable and improved neurologically . In addition, microarray analysis on the chronic plaques of MS patients revealed increased levels of H1R transcripts .
In EAE, higher levels of HA within the cerebrospinal fluid (CSF) correlate with the onset of disease and mast cell granule stabilizers and H1R-specific antagonists reduce EAE severity [25–27]. Importantly, in EAE, Th1 and Th2 clones reactive to proteolipid protein 139–151 have increased levels of H1R and H2R transcripts, respectively. In addition, mice treated with the H1R antagonist pyrilamine or the H2R agonist dimaprit showed reduced clinical severity and pathology [28, 29]. We have previously demonstrated that Bordetella pertussis toxin-induced HA sensitization (Bphs ) is a shared autoimmune disease susceptibility gene in EAE and experimental allergic orchitis, and positional candidate gene cloning identified Bphs to be Hrh1 27]. In addition, gene targeting studies from our lab and other groups demonstrated that HA, H1R, H2R, H3R, and H4R play important roles in EAE susceptibility and pathogenesis, either by regulating encephalitogenic T-cell responses, cytokine production by antigen-presenting cells (APCs), BBB permeability, or T regulatory (Treg)-cell activity [27, 30–34].
The current therapeutic mainstays for MS include IFN-β and glatiramer acetate; however, in most instances, these drugs are of limited efficacy . Consequently, research efforts have been increasingly directed toward identifying new therapeutic modalities and disease-modifying therapies (DMTs). Previously, using individual H1R-H4RKO mice, we showed that H1R and H2R are propathogenic, whereas H3R and H4R are antipathogenic. This suggests that combinatorial pharmacological targeting of HRs may be an effective DMT in MS. To test this hypothesis, we generated H1H2RKO and H3H4RKO mice on the C57BL/6J (B6) background and studied them for susceptibility to EAE elicited by immunization with myelin oligodendrocyte glycoprotein peptide 35–55 (MOG35–55). The results of our study show that compared to B6 mice, H1H2RKO mice exhibit decreased susceptibility to EAE, whereas H3H4RKO mice develop more severe disease. The findings of our study support the concept that combined pharmacological targeting of HRs may be an appropriate DMT in the treatment of MS and other immunopathologic diseases, particularly given the recent development of highly selective agonists and antagonists for H3R and H4R .
EAE was induced in B6, H1H2RKO, and H3H4RKO mice by immunization using a 2× MOG35–55-CFA protocol [37, 38]. The severity of the clinical disease courses differed significantly among the three strains (F =28.5; p< 0.0001) (Fig. 1A), with H1H2RKO mice exhibiting significantly less severe disease than both B6 (F = 17.3; p < 0.0001) and H3H4RKO (F = 57.3; p < 0.0001) mice. In contrast, the severity of the clinical disease course of H3H4RKO mice was significantly greater than B6 (F = 8.2; p< 0.0001) and H1H2RKO (F = 57.3; p < 0.0001) mice. Analysis of EAE-associated clinical quantitative trait variables  revealed that the percentage of animals affected, cumulative disease score, and days affected were significantly greater in H3H4RKO compared with B6 mice. In contrast, percentage of animals affected, cumulative disease score, and days affected were significantly less in H1H2RKO compared with B6 mice (Table 1).
Furthermore, histopathological analysis of the CNS revealed augmented inflammatory responses and pathology in the brains of H3H4RKO mice compared with H1H2RKO and B6 mice (Fig. 1B) with no significant difference in spinal cord pathology (Fig. 1C). Disruption of BBB permeability is another parameter used to assess the neuroinflammatory response in EAE and susceptibility to disease. At day 10 (d10) postimmunization, we found that B6 and H3H4RKO mice had increased BBB permeability during the acute early phase of the disease compared with that of H1H2RKO mice (Fig. 1D). These results indicate that the combined effect of disrupting H1R and H2R signaling is antipathogenic in EAE, whereas the combined effect of disrupting H3R and H4R signaling is propathogenic.
HA and HRs have been shown to be important in regulating hematopoiesis [39–41]. We examined the frequency of different cell types in the primary and secondary lymphoid tissues of naïve B6, H1H2RKO, and H3H4RKO mice. There was no significant difference in the total number of cells in the thymus, lymph node, or spleen among the three strains (Fig. 2A). We also analyzed the frequency of CD4+, CD8+, Foxp3+ Treg, B cell (CD19+), CD11b+, CD11b+Gr1+, NKT (CD1d tetramer+), and NK (NKp46+) cells in primary and secondary lymphoid tissues and found no significant differences in the frequency of these cell types (Fig. 2B, C, D, and E), with the only exception being the lymph node B-cell frequency, which was significantly decreased in H3H4RKO compared with H1H2RKO mice (Fig. 2C). These results strongly suggest that the differences in EAE susceptibility observed between H1H2RKO and H3H4RKO mice are not due to differences in the frequency of immune cells in the primary and secondary lymphoid tissues.
Although the exact pathogenic mechanisms underlying MS and EAE are not known, it is thought to be highly dependent on CD4+ T cells capable of producing IFN-γ and/or IL-17 . HA and HRs play a role in T-cell polarization, proliferation, and cytokine production . Therefore, to elucidate the immune mechanisms associated with differential EAE susceptibility observed in B6, H1H2RKO, and H3H4RKO mice, we compared their MOG35–55-specific T-cell responses on d10 post immunization. In ex vivo proliferation assays, splenocytes and draining lymph node (DLN) cells from all three strains responded equivalently in a dose-dependent fashion to MOG35–55 (Fig. 3A). Splenic and DLN cells from H1H2RKO mice restimulated ex vivo with MOG35–55 produced significantly less IFN-γ (Fig. 3B) and IL-17 (Fig. 3C) compared with restimulated cells from H3H4RKO mice. In addition, H3H4RKO mice produced significantly more IFN-γ and IL-17 compared with B6 mice. IL-4 was undetectable among the three strains. These results suggest that the differences in EAE susceptibility observed in H3H4RKO mice can, in part, be attributed to increased encephalitogenic Th1 and Th17 effector T-cell responses.
Previously, we showed that H1R regulates IFN-γ and IL-4 production by activated CD4+ T cells and Th1/Th2 effector T-cell responses . In the current study, we observed in ex vivo recall assays that splenic and DLN cells from H1H2RKO mice produce significantly less IFN-γ and IL-17 and undetectable levels of IL-4. Therefore, to address whether the lack of the two different classes of HRs have an intrinsic effect on cytokine production or differentiation of CD4+ T cells, we stimulated purified CD4+ T cells from the spleen and lymph nodes of naïve B6, H1H2RKO, and H3H4RKO mice with plate bound anti-CD3 and soluble anti-CD28 mAbs and screened the culture supernatants for IL-17, IFN-γ, IL-4, and IL-2 production by enzyme-linked immunosorbent assay (ELISA) at 24, 48, and 72 h. IL-17 was undetectable among the three strains. Interestingly, across the time points examined, CD4+T cells from H3H4RKO mice produced significantly more IFN-γ compared with cells from H1H2RKO and B6 mice (Fig. 4A). In addition, IL-4 production by stimulated H1H2RKO CD4+ T cells was significantly greater than that of CD4+ T cells from H3H4RKO and B6 mice, which was undetectable (Fig. 4B). Among the strains, we observed no significant difference in the production of IL-2 by CD4+T cells (Fig. 4C). These results indicate that CD4+ T cells from H3H4RKO have an inherent bias toward IFN-γ production, while H1H2RKO are predisposed to produce IL-4. Therefore, the lack of H1R-H2R and H3R-H4R predisposes CD4+T cells to differentiate into either Th2 or Th1 cells, respectively, and may account for the altered cytokine production and differences in disease severity seen among the strains of mice.
The severity of EAE observed in H1H2RKO and H3H4RKO parallels that of the respective individual receptor knockout (KO) mice in that clinical EAE is less severe in both H1RKO and H2RKO mice and more severe in H3RKO and H4RKO mice. Similarly, EAE pathology was significantly less in H1R, H2R and H1H2RKO mice, whereas it was significantly greater in H3RKO, H4RKO, and H3H4RKO mice. The basis of this effect may be due to a compensatory upregulation of the remaining HRs in single HRKO, H1H2RKO, and H3H4RKO mice. With respect to T cells, we showed that HR expression is rapidly downregulated upon T-cell receptor activation, and HR signaling associated with CD4+ T-cell differentiation and effector functions occurs during initial activation . Therefore, we compared HR expression in naïve CD4+ T cells of single HRKO, H1H2RKO and H3H4RKO mice by quantitative real-time polymerase chain reaction (qRT-PCR). H3R expression was undetectable in naïve CD4+ T cells from all single HRKO and H1H2RKO mice. Interestingly, in the absence of single HRs, the expression of the remaining HRs was increased above B6 levels in naïve CD4+ T cells (Fig. 5A). Moreover, H4R expression was increased in H1RKO, H2RKO, and H1H2RKO mice with H1RKO<H2RKO<H1H2RKOs (Fig. 5B). Compared with B6 CD4+ T cells, H1R expression was significantly increased in H3RKO, H4RKO, and H3H4RKO mice with H3RKO< H4RKO< H3H4RKOs (Fig. 5C). Similarly, compared with B6 cells H2R expression was significantly increased in H3RKO, H4RKO, and H3H4RKO mice with H3RKO = H4RKO< H3H4RKOs (Fig. 5D). To address whether compensation by the upregulated HRs in H1H2RKO and H3H4RKO CD4+ T cells affects the expression of HDC or the production of HA, anti-CD3, and soluble anti-CD28 mAb stimulated CD4+ T cells were analyzed for HDC expression (Fig. 5E) by qRT-PCR and screened for HA production by enzyme immunoassay (EIA) (Fig. 5F) at 24, 48, and 72 h. Surprisingly, we did not detect a significant strain effect or (strain × time) interaction for HA production or HDC expression. These data therefore do not support the existence of a compensatory loop with respect to HA production and HDC expression by H1H2RKO and H3H4RKO CD4+ T cells. However, the HR expression studies clearly indicate that disease severity in H1H2RKO and H3H4RKO mice is associated with compensatory upregulation of the corresponding receptors.
Here, we have assessed the overall contribution to EAE susceptibility imposed by H1R and H2R (couple via stimulatory G proteins) and the H3R and H4R (couple via inhibitory G proteins). The results of our study demonstrate that H3H4RKO mice develop a significantly more severe clinical disease course compared with B6 and H1H2RKO mice in association with greater pathology in the brain but not the spinal cord. In contrast, despite a significant difference in the severity of the clinical disease courses between B6 and H1H2RKO, a significant difference in pathology was not detected in either the brain or spinal cord, suggesting as in H3RKO mice , H1R and/or H2R may also play a significant role in central functions related to the severity of clinical signs. Increased susceptibility to EAE in H3H4RKO mice is associated with significantly higher production of IFN-γ and IL-17 in MOG35–55 specific ex vivo recall assays. In contrast, H1H2RKO mice exhibit decreased susceptibility to EAE and decreased BBB permeability. We have also shown that CD4+ T cells from H1H2RKO mice, upon in vitro activation, have an intrinsic immune deviation toward the Th2 phenotype, while activated T cells from H3H4RKO mice have an intrinsic immune bias toward Th1 type cells.
The results of our current study indicate that HA signaling through H1R and H2R augments EAE susceptibility by influencing antigen-specific T-cell effector responses, immune deviation, and BBB permeability. It is well known that HA and HRs modulate the innate and adaptive immune systems . Previously, we have shown that H1RKO mice develop less severe EAE that was associated with an immune deviation of the CD4+ T-cell population from an encephalitogenic Th1 response to a protective Th2 response [27, 31]. In addition, mice deficient for H2R are significantly less susceptible to acute early phase EAE and T cells from immunized H2RKO mice exhibit blunted Th1 effector cell responses . Similar to H1R, HA acting through H2R determines T-cell effector functions and their polarization. T cells from H2RKO mice stimulated in vitro with anti-CD3 and anti-CD28 mAbs produce higher intracellular levels of IFN-γ, IL-4, and IL-13 . Although the mechanism by which H1R and H2R regulates T-cell effector function is poorly understood, possible mechanisms include multiple signaling through HRs, receptor density on a particular cell type, the use of different second messenger molecule/pathways or direct/indirect effect on T cells, APCs, or both. Therefore, while H1R and H2R signaling clearly influences CD4+ T-cell differentiation and effector functions, HR signaling may also contribute to EAE pathogenesis by acting in other cells types associated with disease and remains the subject of future studies.
Pathophysiology associated with MS is thought to be initiated by peripheral autoreactive T cells that cross the BBB and elicit neuroinflammation or autoimmune responses that are secondary to the events initiated by the CNS tissue . Unlike other HRs, H3R is expressed primarily on nonhematopoietic cells. It is predominantly expressed presynaptically and regulates the release of HA and other neurotransmitters. H3RKO mice develop significantly more severe acute early phase disease, neuropathology, and increased BBB barrier permeability compared with B6 mice. T cells from H3RKO mice restimulated ex vivo with MOG35–55 had greater expression of MIP-2, IP-10, and CXCR3 with no significant difference in the Th1, Th2, or Th17 cytokine production . H4R expression is confined mainly on hematopoietic cells and its activation can result in actin polymerization, upregulation of adhesion molecules, and chemotaxis of many immune cells [44–46]. However, recently H4R has been shown to be functionally expressed in the CNS . H4RKO mice develop more severe MOG35–55 induced EAE, augmented neuroinflammation, and increased BBB permeability compared with B6 mice. Similar to H3RKO mice, H4RKO mice had no effect on the production of Th1, Th2, or Th17 cytokines in ex vivo recall assays .
Based on the phenotypes observed in the single HRKO animals, it was surprising for us to find no difference in the production of IFN-γ by H1H2RKO CD4 T cells in ex vivo recall assays, nor a difference in BBB permeability in H3H4RKO mice. Importantly, however, H1H2RKO mice had a significant decrease in BBB permeability while H3H4RKO mice had significantly increased production of IFN-γ and IL-17 compared with B6 mice. The observed phenotypes in H1RKO and H2RKO mice parallels the phenotypes seen in H3H4RKO mice while the H3RKO and H4RKO phenotypes mimic those of H1H2RKO mice. The basis of this yin-yang effect is unknown but may be due to differential cross-regulation of HR expression. Here, we show that in the absence of a single HR, the expression of the remaining HRs is increased above B6 levels in CD4+ T cells. In addition, we demonstrate that in the absence of both H1R and H2R, there is a compensatory upregulation of H4R expression, and in the absence of both H3R and H4R there was upregulation of the H1R or H2R. Importantly, the compensatory upregulation of single HRs in H1H2RKO and H3H4RKO mice may explain the opposing results obtained using pharmacological approaches, where agonists of H1R and H2R inhibited proliferation and cytokine production by antigen-specific T cells and the H2R agonist dimaprit reduced the severity of EAE [29, 47]. In contrast, we can exclude an effect of a T-cell HDC-HA compensatory loop on the HRKO EAE phenotypes since HR expression does not affect HDC expression or HA production by activated CD4+ T cells from B6, H1H2RKO, and H3H4RKO mice.
HA has a long history as a DMT in MS and is purported to improve electrical conductance through demyelinated axons, actively/passively enhance myelin repair and remyelination, and increase the oxygenation of affected CNS tissues by influencing cerebrovascular blood flow and perfusion [48, 49]. HA signaling through its receptors is highly complex and diverse because of the number of receptors, the relative proportion of the receptor subtypes on a given cell type, differences in receptor affinity, and due to the concentration of HA in the local microenvironment.
In this study, we used a dual-gene KO approach to understand the role of HRs coupled to second messenger signaling pathways via stimulatory and inhibitory G proteins as potential targets for effective DMT in MS. Previous epidemiological and clinical studies indicate that the use of H1R-specific blockers is associated with decreased MS risk or stabilization of the disease in MS patients [22, 23]. HA, acting through H2R, can regulate MHC class II expression on immunoreactive cells and the receptor antagonist ranitidine has been used as a long-term therapy in controlling autoimmune psoriasis . Our results presented here indicate that administering antagonists of both H1R and H2R simultaneously may be protective in CNS disease due to the upregulation of the antipathogenic H3R and H4R. Results of the present study indicate that the absence of H3R or H4R signaling has a negative effect on EAE susceptibility and encephalitogenic T-cell activity, suggesting that agonists for this class of receptors may have a beneficial effect in the treatment of CNS autoimmune diseases by overriding HA signaling through the propathogenic H1R and H2R. Therefore, the combined pharmacological targeting of each HR may prove to be an appropriate ancillary DMT in the treatment of MS.
There is an increasing need for new DMT in the treatment of MS and other immunopathologic diseases. Although the lack of specific and highly selective agonists or antagonists for H3R and H4R have precluded their targeting in the clinical treatment of disease, research in recent years has progressed to the point where their use in the clinic is highly likely. Our results, using HR KO mice that couple to two distinct classes of G proteins (stimulatory vs. inhibitory), support the concept of pharmacological targeting of all four HRs along with mainstream drugs like IFN-β or glatiramer acetate as an effective DMT in MS.
C57BL/6J (B6) mice were purchased from the Jackson Laboratory (Bar Harbor, ME). B6.129P-Hrh1tm1Wat (H1RKO) , B6.129P-Hrh2tm1Wat (H2RKO) , B6.129P2-Hrh3tm1Twl (H3RKO) , and B6.129P-Hrh4tm1Thr (H4RKO) mice (generated by Lexicon Genetics, Woodlands Park, TX)  were maintained at the University of Vermont (Burlington, VT). All strains were backcrossed to the C57BL/6J background for at least 10 generations. Individual HRKO mice were interbred and the resulting F1 mice were intercrossed together to generate H1H2RKO and H3H4RKO mice. The experimental procedures used in this study were approved by the Animal Care and Use Committee of the University of Vermont.
Mice were immunized for the induction of EAE using a 2× immunization protocol. The animals were injected subcutaneously in the posterior right and left flank with a sonicated phosphate-buffered saline (PBS)/oil emulsion containing 100 µg of MOG35–55 and CFA (Sigma-Aldrich, St. Louis, MO) supplemented with 200 µg of Mycobacterium tuberculosis H37Ra (Difco Laboratories, Detroit, MI). One week later, all mice received an identical injection of MOG35–55-CFA . Mice were ranked scored daily for clinical quantitative trait variables beginning at day 5 after injection as follows: 0, no clinical expression of disease; 1, flaccid tail without hind limb weakness; 2, hind limb weakness; 3, complete hind limb paralysis and floppy tail; 4, hind leg paralysis accompanied by a floppy tail and urinary or fecal incontinence; 5, moribund. Assessments of clinical quantitative trait variables were performed as previously described .
Histopathological evaluations were done as previously described . Briefly, brains and spinal cords were dissected on 30th day postimmunization, from calvaria and vertebral columns, respectively, and fixed by immersion in 10% phosphate-buffered formalin (pH 7.2). After fixation, trimmed and representative transverse section-embedded in paraffin and mounted on glass slides. Sections were stained with hematoxylin and eosin for routine evaluation and Luxol fast blue-periodic acid-Schiff reagent for demyelination. Representative areas of the brain and spinal cords were selected for histopathological evaluation. The following components of the lesions were assessed: (i) severity and extent of the lesion; (ii) extent and degree of myelin loss and tissue injury (swollen axon sheaths, swollen axons, and reactive gliosis); (iii) severity of the acute inflammatory response (predominantly neutrophils); and (iv) severity of the chronic inflammatory response (lymphocytes/macrophages). Lesions in the brain and spinal cord (SC) were evaluated separately and assigned a numerical score based on a subjective scale ranging from 0 to 5. A score of 0 indicates no lesions; 1 indicates minimal; 2, mild; 3, moderate; 4, marked; and 5, severe lesions.
BBB permeability was assessed as previously described . Briefly, a 50 µg/g dose of FITC-labeled BSA (Sigma, St. Louis, MO) was injected i.v. into B6, H1H2RKO, and H3H4RKO mice on d10 post immunization. CSF and blood were collected after 4 h. Both CSF and plasma samples, prepared by centrifugation at 3000 rpm for 15 min, were diluted in PBS, and the fluorescence intensity was measured with a microplate fluorescence reader (Flx-800-I, Bio-Tek Instruments Inc., Winooski, VT) using the software KC-4, with an excitation wavelength of 485 nm and an emission wavelength of 528 nm. The BBB permeability index is expressed as the ratio of the fluorescence intensity of the CSF (ICSF) divided by the fluorescence intensity of the plasma (IBlood).
For ex vivo cytokine assays, spleen and DLNs were obtained from d10 immunized mice. Single-cell suspensions at 1 × 106 cells/mL in RPMI 1640 medium (Cellgro Mediatech, Manassas, VA) plus 10% FBS (HyClone) were stimulated with 50 µg of MOG35–55. Cell culture supernatants were recovered at 72 h and assayed for IFN-γ, IL-4, and IL-17 by ELISA.
Mice were immunized for EAE induction, and spleen and DLNs were harvested on d10. Single-cell suspensions were prepared, and 5 × 105 cells/well in RPMI 1640 (10% FBS) were plated on standard 96-well U-bottom tissue culture plates and stimulated with 0, 1, 2, 10, and 50 µg of MOG35–55 for 72 h at 37°C. During the last 18 h of culture, 1 µCi of [3H] thymidine (PerkinElmer) was added. Cells were harvested onto glass fiber filters and thymidine uptake was determined with a liquid scintillation counter.
From the DLNs and spleen, CD4+ T cells were isolated by negative selection as previously described (Qiagen, Valencia, CA) . In culture, purified CD4+ T cells (1×106 cells/mL) were stimulated with anti-CD3 (5 µg/mL) and anti-CD28 (1 µg/mL) mAbs (BD Biosciences-Pharmingen, San Jose, CA) for different time points (24, 48, and 72 h) and supernatants were analyzed for IFN-γ, IL-2, IL-4, and IL-17 production by ELISA using anti-IFN-γ, anti-IL-2, anti-IL-4, and anti-IL-17 mAbs and their respective biotinylated mAbs (BD Biosciences-Pharmingen, San Jose, CA).
Single-cell suspensions of thymocytes, lymph node cells, and splenocytes were prepared and the red blood cells were lysed with ammonium chloride. Total numbers of cells were counted using the Advia 120 hematology analyzer (Bayer/Siemens, Tarrytown, NY). For flow cytometric analysis, the cells were washed twice and incubated for 30 min on ice with the desired fluorochrome-conjugated mAbs or isotype control immunoglobulin at 0.5 µg/106 cells. For the identification and phenotypic analysis of TR cells (CD4+CD8−TCRβ+Foxp3+), the following surface antimouse mAb were used: anti-CD4 (MCD0417, Caltag), anti-CD8, and anti-CD25 (53–6.7, PC61; BD Pharmingen, San Jose, CA); anti-TCRβ, and anti-Foxp3 staining set (H57-5987 and FJK-16s; eBioscience, San Diego, CA), according to the manufacturer’s instructions. Viable cells were selected for flow cytometric analysis (LSR II, BD) based on forward and side scatter properties and analysis was performed using FlowJo software (TreeStar Software, Inc.).
Total RNA was extracted from naïve and anti-CD3 + anti-CD28 mAbs stimulated CD4+ T cells from naïve wild-type (WT) and H1–4RKO, H1H2RKO, and H3H4RKO mice using RNeasy isolation reagent (Qiagen Science, MD), and reverse transcribed using Superscript III reverse transcriptase (Invitrogen, Carlsbad, CA). The generated cDNA was used in qRT-PCR using the SYBR green method. The sequences of primers used were as follows:
Hrh1—forward, 5′ TTGAACCGAGAGCGGA 3′; reverse, 5′ TGCCCTTAGGAACGAAT, Hrh2—forward, 5′ TGGCACGGTTCATTCC3′; reverse, GCAGTAGCGGTCCAAG3′, Hrh3—forward, 5′ TGCCTCCTCAGTCTTCAACA 3′; reverse, 5’CCTTCTACCGTGACCAC3′, Hrh4—forward, 5′ TGAGGAGAATTGCTTCACGA 3′; reverse, 5′ TGCATGTGGAGGGGTTTTAT 3′, and for Hdc TaqMan® primers and probes were from Applied Biosystems. β2-microglobulin was used as a reference gene and the relative expression levels were calculated using the comparative threshold cycle (CT) method.
HA concentrations were assessed using an EIA HA kit according to the manufacturer’s instructions (Cayman Chemicals, Ann Arbor, MI). Briefly, 50 µL of derivatization buffer was added to 200 µL undiluted supernatants followed by the addition of 20 µL derivatization reagent. The samples, controls, and standards were added in duplicate to the plate, 100 µL of HA AChE tracer was added to each well, and the plate was incubated at 4°C for 24 h. The wells were washed and 200 µL Ellman’s Reagent was added and incubated for 30 min in the dark at room temperature while shaking. The plate read at 405 nm when the maximum binding control wells reached an absorbance of 0.2–0.8.
Statistical analyses were performed using GraphPad Prism 5 software (GraphPad software Inc., San Diego, CA). Significance of differences was determined as described in the Figure legends.
We thank Dr. Dimitry N. Kremenstov and all the members of the Teuscher lab for helpful discussions; the staff at the University of Vermont DNA sequencing facility for assistance with qRT-PCR. We also thank Dr. Robin L Thurmond, Dr. Timothy W Lovenberg, and Johnson and Johnson Pharmaceutical Research and Development, LLC, San Diego, CA, USA for providing us with H3RKO and H4RKO mice. This work was supported by National Institute of Health Grants NS061014, AI041747, NS060901, NS036526, and NS069628 (to C. T).
Conflict of interest: The authors declare no financial or commercial conflict of interest.