NMP4 regulates the innate immune response to influenza A virus infection.

Severe influenza A virus infection typically triggers excessive and detrimental lung inflammation with massive cell infiltration and hyper-production of cytokines and chemokines. We identified a novel function for nuclear matrix protein 4 (NMP4), a zinc-finger-containing transcription factor playing roles in bone formation and spermatogenesis, in regulating antiviral immune response and immunopathology. Nmp4-deficient mice are protected from H1N1 influenza infection, losing only 5% body weight compared to a 20% weight loss in wild type mice. While having no effects on viral clearance or CD8/CD4 T cell or humoral responses, deficiency of Nmp4 in either lung structural cells or hematopoietic cells significantly reduces the recruitment of monocytes and neutrophils to the lungs. Consistent with fewer innate cells in the airways, influenza-infected Nmp4-deficient mice have significantly decreased expression of chemokine genes Ccl2, Ccl7 and Cxcl1 as well as pro-inflammatory cytokine genes Il1b and Il6. Furthermore, NMP4 binds to the promoters and/or conserved non-coding sequences of the chemokine genes and regulates their expression in mouse lung epithelial cells and macrophages. Our data suggest that NMP4 functions to promote monocyte- and neutrophil-attracting chemokine expression upon influenza A infection, resulting in exaggerated innate inflammation and lung tissue damage.

Introduction

Respiratory illnesses caused by pan class="Species">influenza virus infection are one of the most common health threats in the world. Seasonal influenza results in about 3–5 million illnesses and 290,000 to 650,000 deaths every year. In the United States alone, at least 140,000 hospitalizations are estimated annually since 2010, representing a major impact on public health and economic burden.

Among the four types of viruses (A, B, C, D), influenza A viruses (IAV) account for most pandemics. The primary target of IAV is the airway and alveolar epithelial cells that cover the whole mucosal surface to provide the first line of defense against the inhaled pathogens[1]. In addition to acting as a physical barrier, airway epithelial cells actively regulate both innate and adaptive immunity through the production of pro-inflammatory cytokines and chemokines that recruit and activate innate immune cells such as monocytes/macrophages and neutrophils to the lungs[2-4]. The subsequently activated adaptive immunity contributes to virus clearance and long-term protection[5-8]. While adequate pan class="Species">influenza-induced inflammation is indispensable for the priming adaptive immune responses and control of virus proliferation, a growing number of studies suggest that exaggerated inflammation is associated with lung damage and death[9]. Indeed, patients with severe disease have extensive inflammatory infiltrates and increased cytokine production[10]. Mice deficient in some cytokines or their receptors show reduced morbidity and delayed mortality[11, 12]. Therefore, maintaining a balance between eliminating the virus and controlling excessive inflammation is critical.

Nuclear matrix protein 4 (pan class="Gene">NMP4), also known as CAS-interacting zinc finger protein (CIZ) or Zinc finger protein 384 (ZNF384), was initially characterized as a parathyroid hormone (PTH)-responsive nuclear matrix architectural transcription factor that regulates gene activity by bending DNA[13-15]. Nmp4-deficient mice challenged with anabolic stimuli such as PTH and BMP2 showed enhanced and accelerated bone formation[13, 16–19]. In addition, Nmp4-deficiency resulted in sporadic infertility of male mice due to increased occurrence of spermatogenic apoptosis[20]. Though expressed in a broad spectrum of tissues, its roles in the immune system are barely studied. Recently, Nmp4 has been identified as a fusion partner with several genes to be associated with a subgroup of B-cell precursor acute lymphoblastic leukemia in childhood, with a frequency of approximately 3–4%[21-24]. Nmp4-deficiency reduced the severity of serum-induced arthritis[25]. NMP4 protein directly binds to pro-inflammatory cytokine IL-1β promoter and activates its transcription, suggesting that Nmp4 plays a role in regulating tissue inflammation[25].

In this study, we demonstrated that Nmp4-deficient pan class="Species">mice were protected against H1N1 influenza A virus infection with significantly reduced body weight loss. The Nmp4-deficient mice had comparable viral clearance and adaptive immune responses to IAV infection but significantly fewer monocytes and neutrophil infiltration, and lower pro-inflammatory cytokine and chemokine production compared with wild type mice. NMP4 in both lung structural cells and hematopoietic cells contributes to monocytes and neutrophil recruitment after influenza infection. We further demonstrated that NMP4 bound to the promoter and/or conserved non-coding sequences of chemokines Ccl2, Ccl7 and Cxcl1 to regulate their expression in mouse lung epithelial cells and bone marrow derived macrophages. Taken together, our data suggest that Nmp4 participates in airway mucosal innate immune responses to influenza A viruses through regulation of chemokine expression in lung epithelial cells and macrophages.

Results

Nmp4−/− mice showed reduced body weight loss after influenza infection.

NMP4 is a zinc finger containing transcription factor and has been shown to bind to the promoter of the pan class="Gene">Il1b gene to regulate its expression[25]. RNA-Seq analysis of the transcriptome in mesenchymal stem/progenitor cells[26] revealed that Nmp4-deficiency significantly altered expression of genes of several pathways involved in immune responses (Fig. S1A). Notably, the expressions of several chemokines were significantly changed (Fig. S1B). We, therefore, hypothesize that NMP4 plays a role in host defense against pathogens.

To characterize the role of NMP4 on anti-viral immune responses, we pan class="Disease">infected wild type (WT) and Nmp4-deficient mice with a sublethal dose of influenza virus strain A/Puerto Rico/8/1934 (PR8) and recorded their body weight loss. Nmp4 knockout mice showed less morbidity and lost only 5% of original body weight compared to 20% of weight loss in WT mice (Fig. 1A). Surprisingly, quantitative RT-PCR (qRT-PCR) analysis of viral nucleoprotein (NP, Fig 1B) and polymerase (PA, Fig. S2A) RNA showed no difference in viral load in the lungs of Nmp4-deficient and WT mice at both 4 and 7 days post-infection (dpi), although Nmp4-deficient mice had slightly but significantly lower viral load at 10 dpi (Fig. 1B). Similar results were obtained by measuring the infectious virions in the bronchoalveolar lavage (BAL) fluid collected from mice (Fig. 1C and Fig. S2B). These data suggested that the reduced susceptibility of Nmp4-deficient to IAV infection was not due to a difference in viral clearance.

Figure 1.

Nmp4 deficiency reduces disease severity after H1N1 (PR8) influenza virus infection in mice.

(A) Body weight changes of mice after infection (n = 10 – 12 mice). (B) Realtime PCR quantification of influenza virus NP gene expression (relative to reference gene B2m) in the lung tissues at specified time points. (C) Viral titer in bronchoalveolar lavage fluid (n = 10 – 12 mice). Data represent mean ± SEM from one of four independent experiments. *: p < 0.05; **: p < 0.01; ***: p < 0.001 by two-way ANOVA with Bonferroni post-test (A&C) or two-tailed t-test (B).

Nmp4 is not required for adaptive immune responses to IAV infection

The adaptive immune responses are critical to protecting the host from influenza pan class="Disease">virus infection as Rag-deficient mice failed to clear the virus resulting in sustained airway damage and death[27]. To understand the mechanisms of enhanced protection in Nmp4-deficient mice, we first examined the adaptive immune responses to influenza infection. T cell responses normally peak at 6–9 days post-infection then resolve, whereas serum and mucosal antibody titers are sustained for a longer time[28]. BAL fluid, lungs, lung-draining mediastinal lymph nodes (dLN) and spleens were collected from virus-infected mice at 7 and 10 dpi and stained with virus-specific tetramers to elucidate CD8 and CD4 T cell responses both locally and globally. Three of the five lung lobes were digested with collagen and DNAse, disassociated with C tubes on a gentleMACS Dissociator (Miltenyi). The cells were stained with fluorescence-conjugated antibodies immediately and analyzed with flow cytometry (Fig. 2A). No significant differences were observed in the percentage of PA-tetramer positive CD8 T cells at 7 or 10 dpi (Fig. 2B). Similarly, total CD4 T cells in different tissues were also comparable between wild type and Nmp4-deficient mice (Fig. 2C).

Figure 2.

Nmp4 deficiency does not affect adaptive immune response to influenza infection in mice.

(A) Gating strategy to identify CD4, CD8, and virus-specific (PA Class I tetramer) CD8 T cells in influenza infected lung. (B) Flow cytometric analysis of PA+ CD8 T cells in specified tissues at 7 and 10 dpi. (C) Flow cytometric analysis of total CD4 T cells in specified tissues at 7 dpi. (D) Flow cytometric analysis of IFN-γ expression by CD8 and CD4 T cells in the lung. (E) Flow cytometric analysis of TNF-α expression by CD8 and CD4 T cells in the lung. (F) Flow cytometric analysis of IFN-γ and TNF-α expression by virus-specific PA+ CD8 T cells in the lung. (G) Gamma interferon mRNA (Ifng) expression in the lung tissue was detected by qRT-PCR (n = 10 – 12 mice). Ifng mRNA expression was normalized to B2m expression. (H) Interferon gamma concentration in bronchoalveolar lavage fluid (BALF) obtained at 7 dpi. Data represent mean ± SEM from one of two independent experiments. n = 10 mice for B and C. For D - F, plots were gated on live cells negative for Zombie dyes to minimize the interference of cells died during PAM and ionomycin re-stimulation. BAL: Bronchoalveolar lavage; dLN: Lung draining lymph nodes; Spl: Spleen.

Since CD8 and pan class="Gene">CD4 T cells contribute to viral control by producing effective cytokines, such as IFN-γ[6, 8], we wondered whether Nmp4 deficiency could possibly change the functionality of T cells in the infected lung. Mononuclear cells in lung single cell suspensions at day 10 post-viral infection were further isolated by Ficoll gradient centrifugation, and re-stimulated with phorbol 12-myristate 13 acetate (PMA) and ionomycin followed by the intracellular cytokine staining to examine IFNγ and TNFα production in lung infiltrating CD8 and CD4 T cells. Percentages of IFN-γ+ (Fig. 2D) and TNF-α+ (Fig. 2E) CD8 and CD4 T cells were similar in Nmp4-deficient and WT mice. We further examined cytokine production by virus-specific CD8 T cell in the lung using PA MHC class I tetramer provided by NIH Tetramer Core Facility at Emory University. No differences in IFN-γ and TNF-α production by PA+ CD8 T cells were observed (Fig. 2F). We further examined gamma interferon mRNA (Ifng) expression in the lungs of mice after IAV infection by quantitative RT-PCR. Ifng mRNA expression in both WT and Nmp4−/− mice was upregulated at 7 dpi as adaptive immune responses reached a peak, yet no differences in expression levels were detected between these mice (Fig. 2G). ELISA quantification of IFN-γ in bronchoalveolar lavage fluid (BALF) also showed no difference.

Next, we assessed virus-specific antibodies in sera from virus-infected pan class="Species">mice ELISA. WT and Nmp4 deficient mice exhibited the similar amount of virus-specific IgG (Fig. 3A) and IgM (Fig. 3B) antibodies against the virus at both 7 and 10 dpi, indicating Nmp4-deficiency does not change B cell function and humoral immunity upon influenza virus infection. Taken together, our data suggest that NMP4 is not required for adaptive immune responses to influenza infection.

Figure 3.

Nmp4 deficiency does not affect humoral immune response to influenza infection in mice.

(A) ELISA quantification of serum influenza virus-specific IgG at 7 and 10 dpi. (B) ELISA quantification of serum influenza virus-specific IgM at 7 and 10 dpi. Data represent mean ± SEM (n = 10 – 12 mice) from one of two independent experiments. ns: not significant by one way ANOVA with Bonferroni post-test.

Reduced pro-inflammatory cytokine expression in lungs of Nmp4 deficient mice.

During influenza infection, signals of pan class="Disease">infection recognized by pattern recognition receptors (PRRs) lead to the production of pro-inflammatory cytokines and chemokines[4, 29]. An increasing number of studies suggested that pro-inflammatory cytokines and chemokines not only contribute to protective anti-viral immunity but also associate with tissue pathology and disease severity. Excessive cytokine production, termed cytokine storm, characterized by higher levels of pro-inflammatory cytokines and chemokines, is observed in patients hospitalized with severe influenza infections[10]. For example, IL-1β was induced by influenza infection and blockade of IL-1β receptor alleviated H1N1 induced inflammation[30]. Similarly, IL-6 was associated with flu driven pathology[10], even though studies also demonstrated the protective roles of IL-6 in promoting anti-viral immune responses[31, 32].

We first examined pro-inflammatory cytokine expression in the lungs of IAV infected pan class="Gene">Nmp4-deficient and WT mice. We found that Il1b but not Il1a mRNA expression in the lungs of Nmp4−/− mice was significantly lower at 4 days post-infection comparing to that in the WT mice (Fig. 4A). Similarly, reduced Il6 mRNA expression in the lung tissue and IL-6 in BALF of Nmp4−/− mice were also observed at 4 dpi (Fig. 4B). Expression of other cytokines known to be involved in anti-viral immunity[11, 33–35] including tumor necrosis factor (Tnf, Fig. 4C) and type I interferons (Ifna1 and Ifnb, Fig. 4D) was not affected by Nmp4 deficiency.

Figure 4.

Effects of Nmp4 deficiency on expression of cytokines in the lung tissues after influenza virus infection.

(A) qRT-PCR detection of Il1b and Il1a in lung tissues. (B) qRT-PCR detection of Il6 in lung tissues and ELISA measurement of IL-6 in BALF. (C) qRT-PCR detection of Tnf in lung tissues. (D) qRT-PCR detection of Ifna1 and Ifnb in lung tissues. Data represent mean ± SEM (n = 10 – 12 mice) from one of two independent experiments. *: p < 0.05; ***: p < 0.001 by two-way ANOVA with Bonferroni post-hoc test.

Nmp4 is required for innate immune responses to influenza infection.

Previous studies demonstrated that macrophages and neutrophils migrate rapidly to the airways upon influenza infection 2 and contribute to both anti-viral immunity and immunopathology[4, 29]. To determine the effects of pan class="Gene">Nmp4 deficiency on innate immune responses, we examined the kinetics of monocytes/macrophages and neutrophils infiltrating into the lungs at increasing time points after infection. Total lung cellularity of Nmp4−/− mice is significantly lower than that of WT mice at 4 and 7 dpi (Fig. 5A). Lung single cell suspensions were stained and analyzed by flow cytometry to phenotype the lung infiltrating myeloid cells (Supplementary Fig. S3). Both lung monocyte and neutrophil counts were significantly decreased in Nmp4 deficient mice compared with WT mice at 4 dpi (Fig. 5B&C), with a trend of reduction of neutrophils at 7 dpi although this did not reach significance. Similarly, a trend towards fewer monocytes and significantly fewer neutrophils were also found in bronchoalveolar lavage fluid (BALF) of Nmp4 deficient mice (data not shown).

Figure 5.

Nmp4 deficient mice showed reduced innate immune response to influenza virus infection.

(A) Total viable cells in lung tissues after collagenase digestion. (B) Flow cytometric analysis of inflammatory monocytes/macrophages in lung tissues. (C) Flow cytometric analysis of neutrophils in lung tissues. (D) Flow cytometric analysis of eosinophils in lung tissues. (E) Flow cytometric analysis of monocytes and neutrophils in bone marrow. (F) Flow cytometric analysis of monocytes and neutrophils in blood. (G) Realtime PCR detection of Ccl2 expression in the lung tissue and ELISA measurement of CCL2 concentration in BALF. (H) Realtime PCR detection of Cxcl1 expression in the lung tissue and ELISA measurement of CXCL1 concentration in BALF. (I) Realtime PCR detection of Ccl7 expression in the lung tissue. Data represent mean ± SEM from one of four (A-D) or two (E-I) independent experiments. n = 10 – 12 mice for A-D & G, and n = 4 mice for E-F. *: p < 0.05; **: p < 0.01; ***: p < 0.001 by two-way ANOVA with Bonferroni post-test (A-G) or two tailed t-test (H & I).

To exclude the possibility that Nmp4 pan class="Disease">deficiency impaired innate cell development, we analyzed monocytes and neutrophils in the bone marrow. The percentages and cell counts of monocytes and neutrophils in the bone marrow were similar between Nmp4−/− and WT mice (Fig. 5E). Furthermore, percentages of monocytes and neutrophils in the blood were also comparable between these mice (Fig. 5F), suggesting the mobilization of these innate cells from bone marrow to blood was not affected by Nmp4 deficiency.

Chemokines guide the migration of immune cells into the lung after infection. Consistent with reduced monocyte and neutrophil infiltration, we found that expression of several chemokines pan class="Gene">Ccl2, Cxcl1 and Ccl7 – known to attract monocytes and neutrophils – was attenuated in the lungs of Nmp4−/− mice at 4 dpi (Fig. 5G–H) at mRNA level. CCL2 and CXCL1 protein concentrations in BALF at 4 dpi were also significantly different (Fig. 5G & H).

Nmp4 in both lung structural cells and hematopoietic cells contributes to monocyte and neutrophil recruitment

Since both lung epithelial cells and hematopoietic cells can secrete chemokines, we wondered which cell type is responsible for reduced innate immune responses after influenza infection. We generated bone marrow chimera pan class="Species">mice by i.v. transfer of congenic marked bone marrow cells into lethally irradiated recipient mice. Bone marrow reconstitution was confirmed by flow cytometric analysis of peripheral blood mononuclear cells (PBMC) (supplementary Fig. S4). Four days after influenza infection, total viable lungs cells in WT to KO group (where WT bone marrow cells were injected into irradiated Nmp4 deficient recipients) were significantly reduced compared to the WT to WT group (Fig. 6A). Although not significant, KO to WT group also showed reduced total viable lung cell counts. Total viable lung cells were further reduced when both lung structural cells and hematopoietic cells deficient for Nmp4 (KO to KO group) (Fig. 6A). Similar results were also seen when we gated on infiltrating monocytes (Fig. 6B) and neutrophils (Fig. 6C) that cell counts were significantly reduced when Nmp4 was deficient in either lung structural cells or hematopoietic cells comparing to WT to WT group, and were further reduced when Nmp4 was deficient in both lung structural cells and hematopoietic cells. Therefore Nmp4 is required in both compartment to regulate anti-influenza innate immune responses in the lung.

Figure 6.

NMP4 in both bone marrow derived cells and lung structural cells regulates Innate immune response to influenza infection.

(A) Total viable cells in lung tissues 4 days after influenza infection. (B) Flow cytometric analysis of inflammatory monocytes/macrophages in lung tissues. (C) Flow cytometric analysis of neutrophils in lung tissues. Data represent mean ± SEM from one of two independent experiments. n = 4 – 5 mice. *: p < 0.05; **: p < 0.01; ***: p < 0.001; ****: p < 0.0001 by one-way ANOVA with Bonferroni post-test.

Nmp4 regulates chemokine expression in mouse lung epithelial cells and bone marrow derived macrophages

Influenza virus primarily targets the respiratory epithelial cells including airway epithelial cells and pneumocytes. pan class="Species">Influenza virus-infected epithelial cells release various chemokines to trigger the recruitment of an array of innate immune cells[29]. Infiltrating monocytes/macrophages also express chemokines to recruit additional monocytes. We first examined NMP4 expression in the mouse lung by immunohistochemistry with a polyclonal rabbit antibody and demonstrated nuclear staining in airway epithelial cells, pneumocytes and macrophages in wild type mice but not Nmp4 deficient mice (supplementary Fig. S5).

We next studied how Nmp4 regulates innate cell attracting chemokine expression in lung epithelial cells and macrophages. We designed three guiding RNAs (gRNA1 – gRNA3) targeting the coding sequences of pan class="Gene">NMP4 N-terminus and cloned into the LentiCRISPR lentiviral vector[36] to edit the Nmp4 gene in MLE-12 cells. MEL-12 cells transduced with the lentivirus expressing one of the gRNA, or mixture of the lentiviruses were cultured for 5 days in the presence of 20 μg/ml puromycin. Expression of NMP4 was examined by Western blot and cells transduced with one of three lentiviruses or their mixture showed reduced expression of NMP4 compared with control cells (Fig. 7A). Although puromycin selection yielded polyclonal lentivirus-transduced cells so that targeted gene would not be edited in 100% cells, gRNA1 showed the highest efficiency in knockdown of NMP4 expression. Therefore, gRNA1 lentivirus-transduced cells were chosen for the following studies. We used ChiP assay to test the binding of NMP4 to the promoters and conserved noncoding sequences (CNS) of Ccl2, Cxcl1 and Ccl7 genes that are down-regulated in influenza infected lungs of Nmp4 deficient mice (Fig. 5G–I). The cells were also stimulated with poly I:C for 6 hours to test the effects of Nmp4 knockdown/knockout on the mRNA expression of these chemokines using realtime PCR. In MLE-12 cells, we found that NMP4 bound to both Ccl2 and Cxcl1 gene loci (Fig. 7B, top and middle panels). Correlating to the NMP4 binding pattern, poly I:C stimulation up-regulated Ccl2 and Cxcl1 mRNA expression and Nmp4 knockdown significantly reduced their expression (Fig. 7C). In bone marrow derived macrophages (BMDM), however, NMP4 did not bind to these two gene loci (Fig. 7D, top and middle panels). While poly I:C induced Ccl2 mRNA expression independent of Nmp4 (Fig. 7E, top panel), it did not induce Cxcl1 expression in BMDM (Fig. 7E, middle panel). Different from Ccl2 and Cxcl1 induction and regulation, Ccl7 expression in MLE-12 was not induced by poly I:C treatment and Nmp4 knockdown showed minimal effect on its expression (Fig. 7C, bottom panel), while NMP4 had strong binding to the Ccl7 promoter region in BMDM (Fig. 7D, bottom panel) and poly I:C treatment induced high Ccl7 mRNA expression that was significantly reduce in Nmp4 deficient BMDM (Fig. 7E, bottom panel).

Figure 7.

NMP4 regulates chemokine expression in mouse airway epithelial cells and bone marrow derived macrophages (BMDM)

(A) Western blot to verify Nmp4 knockdown in mouse lung epithelial cell line (MLE-12) transduced with lentiCRISPR lentivirus containing Nmp4 targeting gRNA and selected with puromycin. (B) ChIP analysis of NMP4 binding to Ccl2, Cxcl1 and Ccl7 loci in MLE-12 cells. (C) Realtime PCR assessment of effects of Nmp4 knockdown on Ccl2, Cxcl1 and Ccl7 expression in MLE-12 cells stimulated with poly I:C for 6 hours. (D) ChIP analysis of NMP4 binding to Ccl2, Cxcl1 and Ccl7 loci in BMDM. (E) Realtime PCR assessment of effects of Nmp4 deficiency on Ccl2, Cxcl1 and Ccl7 expression in BMDM stimulated with poly I:C for 6 hours. (F) Alignment of mouse and human CCL2 gene locus showing gene structure and conserved non-coding sequence. The 2.7 kb fragment was cloned to the pGL4Luc-RLuc dual luciferase reporter vector. (G) Luciferase reporter assay to assess the effect of NMP4 knockdown on Ccl2 promoter activity in MLE-12 cells. Data represent mean ± SEM. n = 4 for ChIP (B&D) and luciferease assay (G); n = 6 for realtime PCR analysis of chemokine expression (C&E). *: p < 0.05; **: p < 0.05 by one-way ANOVA with Bonferroni post-test. Prom: promoter region; CNS: conserved non-coding sequence; CNS−6 and CNS−9.5: conserved non-coding sequences 6 kb and 9.5 kb upstream of Cxcl1 transcription start site; UTR: untranslated region.

To further confirm the regulation of Ccl2 gene activity by pan class="Gene">NMP4, we cloned a 2.7 kb genomic fragment containing the CNS and promoter of the Ccl2 gene into a pGL4Luc-RLuc dual luciferase reporter vector (Fig. 7F) and performed luciferase assay in MLE-12 cells (Fig. 7G). While poly I:C treatment significantly induced Ccl2 CNS+promoter driven luciferase activity, gRNA1 mediated Nmp4 knockdown significantly reduced luciferase activity (Fig. 7G). Similar effects on Ccl2 and Cxcl1 mRNA expression and luciferase activity were also observed in siRNA mediated Nmp4 knockdown MLE-12 cells (supplementary Fig. S6). We also performed Ccl2 luciferase assay in BMDM. Consistent with the NMP4 independent expression of Ccl2 in BMDM (Fig. 7E, top panel), Ccl2 CNS+promoter driven luciferase activity was not reduced in Nmp4−/− BMDM (data not shown). Taken together, our in vitro data indicate that NMP4 is able to bind to Ccl2, Cxcl1 and Ccl7 regulatory elements in mouse lung epithelial cells and/or BMDM to regulate chemokine expression in the lung.

Discussion

An overactive immune response causing severe tissue damage is an important contributor to death during exposure to highly virulent strains of pan class="Species">influenza A such as the 1918 H1N1 virus or highly pathogenic avian H5N1 viruses. Mice infected with the highly pathogenic 1918 pandemic H1N1 virus exhibit significantly higher numbers of monocytes/macrophages and neutrophils in the lungs compared to mice infected with low pathogenic viruses[2]. In this study, we demonstrated that mice deficient in the Nmp4 gene that encodes a zinc figure transcription factor protected mice from H1N1 influenza virus-induced morbidity by recruiting significantly fewer monocytes/macrophages and neutrophils without significant impact on adaptive immune responses and viral clearance. Expression of monocyte and neutrophil attracting chemokines Ccl2, Ccl7, and Cxcl1 was significantly reduced in the virus-infected airways of Nmp4-deficient mice. We further demonstrated that NMP4 in both lung structural cells and hematopoietic cells contributes to monocytes and neutrophil recruitment upon influenza infection. Mechanistically, NMP4 may directly bind to the Ccl2, Cxcl1 and Ccl7 gene loci to regulate the expression of these chemokines in lung epithelial cells and/or macrophages. Our data identify a novel function of NMP4 regulating chemokine expression in airway epithelial cells and macrophages to coordinate antiviral innate immune responses after influenza A virus infection.

Several papers reported that PR8 infection strongly induces the release of pan class="Gene">MCP1 (encoded by Ccl2 gene) followed by monocyte recruitment and that CCL2 receptor-deficient mice displayed abrogated immunopathology[12, 37–39]. In parallel, the CCL2 receptor CCR2-dependent recruitment of inflammatory macrophages contributes substantially to lung damage[40], and administration of a CCL2 blocking antibody can decrease mortality and morbidity following influenza A virus infection[41]. Upon influenza virus infection, airway epithelial cells induce CCL2 expression starting at 1 dpi and inflammatory monocytes/macrophages isolated at 3 dpi also produce CCL2[41]. Nmp4 deficiency does not suppress Ccl2 expression in bone marrow-derived macrophages (Fig. 7E) but the knockdown of Nmp4 expression significantly reduces poly I:C-induced Ccl2 expression in lung epithelial cells (Fig. 7C), strongly suggesting that regulation of influenza virus induced Ccl2 expression by NMP4 is mainly in airway epithelial cells. Similar to our notion that reduced Ccl2 expression in airway epithelial cells is protective to influenza A virus infection, a recent paper also demonstrated that airway epithelial cell-specific A20 knockout mice had decreased CCL2 production and were protected from Influenza A virus infection[42].

Neutrophils are the first immune cells recruited to the site of injury or pan class="Disease">infection. While crucial players in controlling bacterial and fungal infections, less is known for neutrophil function in antiviral immune responses or viral pathogenesis. In a ferret model, the migration of neutrophils into the lung occurs within hours of influenza infection[43]. Depletion of neutrophils prior to infection with influenza A virus leads to increased mortality in mice, suggesting a protective role for neutrophils[44]. Massive infiltration of neutrophils into the lungs during influenza virus infection can result in acute lung inflammation that can be abrogated by Ab-mediated blockade of CXCL1 receptor CXCR2[45]. Similar to the case of inflammatory monocytes/macrophages discussed above, we also found that Nmp4 deficient mice had reduced Cxcl1 expression / CXCL1 production (Fig. 5H) and neutrophil load (Fig. 5C) in the airways upon influenza A virus infection. Knockdown of Nmp4 expression in mouse lung epithelial cells significantly inhibited poly I:C-induced Cxcl1 expression (Fig. 7C, middle panel) that would result in reduced neutrophil influx immediately following IAV infection[43].

Our analysis with bone marrow chimera mice demonstrated that pan class="Species">influenza induced recruitment of monocytes and neutrophils relied on Nmp4 activity in both lung structural cells and hematopoietic cells, Nmp4 deficiency in either compartment resulted in fewer monocytes and neutrophils recruited into the infected lung (Fig. 6). Lung epithelial cells are the primary target of influenza virus infection and source of pro-inflammatory cytokines and chemokines that recruit and activate monocytes[29]. Cytokines and chemokines released from recruited and activated monocytes will further augment inflammation and cell infiltration[29]. Consistent with these results, we found that expression of monocyte-attracting Ccl2 and neutrophil-attracting Cxcl1 in lung epithelial cells are Nmp4 dependent (Fig 7C, top and middle panels). In addition, bone marrow derived macrophages (BMDM) are also significant source of Ccl2 albeit independent of Nmp4 (Fig 7E, top panel) and another monocyte-attracting chemokine Ccl7 is highly induced by poly I:C in BMDM. Reduced Ccl2 expression by Nmp4 deficient epithelial cells leads to reduced monocytes and neutrophil recruitment, and fewer monocytes results in lower Ccl2 and Ccl7 expression further limiting the inflammatory infiltration. To complement to our in vitro studies presented in this manuscript, we are currently crossing our newly generated Nmp4 flox mice to perform detailed analysis to define the role of NMP4 in regulating chemokine and cytokine expression in different cell types during influenza infection.

In conclusion, our studies demonstrate that Nmp4 pan class="Disease">deficiency has no effects on adaptive immune responses but dampens the expression of monocyte- and neutrophil-attracting chemokine Ccl2, Cxcl1 and Ccl7 expression in lung epithelial cells and/or macrophages after influenza infection. The reduction in chemokine production in lung epithelial cells limits the initial infiltration of inflammatory monocytes/macrophages and neutrophils, which in turn will further reduce inflammation and inflammatory cytokine production, thus protect the mice from influenza-induced cytokine storm and tissue damage.

Materials and Methods

Mice and influenza virus infection

Nmp4−/− pan class="Species">mice under C57BL/6J background and their WT littermates were maintained in our colony at Indiana University Bioresearch Facility, Indiana University School of Dentistry. The mouse-adapted influenza virus strain A/PR/8/34 (H1N1) was prepared as described and provided by Dr. Sun’s lab at Mayo Clinic[46]. Mice were infected intranasally with 335 Pfu of PR8 in serum-free DMEM medium (Gibco) after anesthetized with Ketamine/Xylazine.

Preparation of lung cells

Mouse lungs were perfused with 5 ml pan class="Chemical">PBS injected through right ventricle of heart until the lung turned white. Lung lobes were cut into small pieces and incubated in 5 mL HEPES buffer with 0.5mg/mL collagenase type 4 (Worthington) for 45 minutes at 37°C. After digestion, lung tissues were transferred to C-tubes and further dissociated using the gentleMACS Dissciator (Miltenyi Biotec). Tissue samples then were passed through 70 μm cell strainer and washed with HEPES buffer. The red blood cells in lungs were lysed in ACK lysing buffer and resuspended in FACS buffer for flow cytometric analysis.

For intracellular cytokine staining of, lung single cells as prepared above were re-suspended in 4 mL HEPES buffer and 2 mL Ficoll-Paque™ PLUS (GE Healthcare) were gently underlaid. After centrifuing at 1800–2000 rpm for 15 minutes, lung cells at the interface were harvested, washed with pan class="Chemical">HEPES buffer and pelleted in IMDM (Gibco) complete medium containing 10% FBS and 2% penicillin-streptomycin. These cells included both lymphocytes and myeloid cells. They were re-stimulated with PMA and ionomycin for 5 hours and Golgi inhibitor monesin (Biolegend) was added for the last 3 hours, followed by flow cytometry analysis.

cDNA synthesis and real-time PCR

mRNA from culture cells and lung homogenates were isolated with TRIzol reagent (Invitrogen) or RNeasy Mini pan class="Gene">Kit (QIAGEN) following the manufacturer’s instructions. cDNA was synthesized using High Capacity cDNA Reverse Transcriptase Kit (Applied Biosystems). Quantitative real-time PCR was performed with Fast SYBR Green Master Mix (Applied Biosystems) on the 7500 Fast Real-time PCR System (Applied Biosystems). Delta CT values were calculated for each transcript in which β2m mRNA expression was used for normalization.

Virus titer

Madin-Darby canine kidney cells (MDCK) cells were seed in 96-well plate and allowed the cells to grow 80% confluent. Cells were treated with dilutions of BAL fluid from pan class="Disease">virus-infected mice. To generate the standard curve, dilutions of influenza virus stock with known titer were used. After 6-hour incubation at 37°C in a humidified atmosphere with 5% CO2, infection supernatant in each well was removed and cells were washed with sterile PBS twice. Expression of viral gene NP and PA was detected by RT-qPCR. Virus titer was calculated based upon the standard curves of NP or PA expression vs viral titer diluted from virus stock solution (Fig. S2B).

ChIP analysis

Mouse lung epithelial (pan class="CellLine">MLE-12) cells were seeded into the 10cm dish and grew to 80% confluent at a density of 8×106. Cells were cross-linked for 10 min with 1% formaldehyde and lysed by sonication. Cross-linked cells were precleared with herring sperm DNA, bovine serum albumin, and protein A/G plus agarose beads (Santa Cruz Biotechnology). Cell extracts were incubated with 6 μg antibody against NMP4 (Sigma HPA004051) or normal IgG rabbit antibody overnight at 4°C. The immunocomplexes were precipitated with protein A/G agarose at 4°C for 2 hours, washed and eluted. Cross-links were reversed at 65°C overnight. ChIPed DNA was extracted with phenol-chloroform, re-suspended in H2O, and analyzed by quantitative PCR.

Flow cytometry analysis

Cells isolated from the BALF and single cell suspension of lungs were stained with fluorochrome-conjugated antibodies CD45, pan class="Gene">CD11b, Ly6G, F4/80, CD11c, CD4, CD8 (Biolegend), SiglecF (BD Biosciences) or MHC-I tetramers, MHC-II tetramer (NIH Tetramer Core at Emory University). Cells were incubated with fluorochrome-conjugated antibodies for 30 minutes at room temperature prior to washing and fixing with 1% formaldehyde. For intracellular cytokine staining, splenocytes were re-stimulated with PMA and ionomycin for 5 hours and Golgi inhibitor monesin (Biolegend) was added for the last 3 hours. After re-stimulation, cells were stained with surface marker including viability dye, washed, fixed and permeabilized and stained with intracellular antibody IFN- γ (Biolegend) for 1 hour. Stained cells were analyzed on an Attune Flow Cytometer (Thermo Fisher).

CRISPR/Cas9 mediated NMP4 knockdown in MLE-12 cells

To knockdown NMP4 expression in pan class="CellLine">MLE-12 cells, we identified three gRNAs targeting the N-terminus of NMP4 as following: 5’- ATGAGTCCTGTAGATGGTAC-3’, 5’- TCAATTCTAACCCGTACTTC-3’ and 5’- ACGTAAGGGTCATTCATCTC-3’. DNA oligomers corresponding to these gRNAs were synthesized by IDT and annealed DNA oligomers were inserted to the downstream of U6 promoter of LentiCRISPRv2 plasmid (Addgene, plasmid # 52961) as described[36]. Lentivirus were generated by co-transfection the LentiCRISPRv2, PAX2, and PMDG.2 plasmids into HEK 293 T cells using lipofectamine 3000 reagent (Invitrogen). Lentivirus was harvested 36 to 48 hours after transfection and filtered through 0.45 μm filter for immediate use or store at 4 °C for at most 24 hours.

Mouse lung epithelial cells (pan class="CellLine">MLE-12) were culture in 6-well plate in HITES media until 90% confluency. Culture media were replaced with 1 to 2 mL fresh HITES media and 1mL DMEM medium containing lentivirus collected above. Cells were infected with lentivirus by centrifuged at 2000rpm for 45 mins with the presence of 8 μg/mL polybrene (Sigma-Aldrich). After spin, cells were incubated in 37 °C, 5% CO2 overnight. The next morning, target cells were changed back to fresh HITES media for expansion for at least 6 hours. To select infected cells, 2 μg/mL puromycin was added to the media for 3–5 days when non-infected MLE-12 cells that treated with same concentration of puromycin were all dead.

Western blot confirmation of NMP4 knockdown

MLE-12 cells were washed with pan class="Disease">cold PBS and lysed in 200 μl RIPA buffer containing protein inhibitors. Cells were then scraped in to 1.5 mL microfuge tube and sonicate for 10 seconds. Lysates were spined at 10,000 rpm for 10 mins and the supernatants were transferred to clean tubes. Protein concentration was determined by Pierce™ Detergent Compatible Bradford assay kit (Thermo Fisher Scientific) following the manufacturer’s instructions.

Sample buffer (4X) containing DTT was added into each sample (final 1X) and heated at 100 °C for 8–10 mins. 20–30 μg samples in 20–30 μL were loaded to the Mini-Protein TGX gels (Bio-pan class="Gene">Rad) and run at 200V for about 1~ 1.5 hours. After running, proteins were transfer to nitrocellulose membrane through the half-wet system at 200–400 mA for 30 mins. The membrane was blotted with rabbit anti-mouse NMP4 antibody (1:1000 dilution) or mouse anti-actin IgG (1: 500 dilution) overnight at 4°C and imaged with ChemiDoc MP Imaging System (BioRad).

Generation of bone marrow derived macrophages

For the generation of bone marrow-derived macrophages (BMDM), bone marrow cells were cultured in complete DMEM medium with 10% FBS, 2% pan class="Chemical">penicillin-streptomycin, 2 mM L-glutamine, 0.1 mM 2-Mercaptoethanol and 40 ng/mL M-CSF for 7 days.

Luciferase reporter assay

A 2.7kb fragment containing the conserved non-coding sequence (CNS) and promoter of Ccl2 gene were amplified from pan class="Species">mouse genomic DNA using the following primers. 5’-GCTAGCCTCGAGTGATGTTCTATCAGTCCTCACCCCATTAC-3’, 5’- GAGGCCAGATCTCTCTGAGGCAGCCTTTTATTGTTAGCCAG-3’. The amplified fragment was digested with restriction enzymes XhoI and BglII and cloned into pGL4Luc-Rluc dual luciferase plasmid (Addgene, plasmid #64034).

MLE-12 cells, control cells or pan class="Gene">NMP4 knockdown cells, were culture in 24-well plate until 80% confluency and then transfected with pGL4Luc-Rluc vector or reporter plasmid using TransIT-2020 reagent (Mirus). After 24 hours of incubation in transfection complex, cells were stimulated with poly (I:C) (5μg/mL) for 6 hours and cell extracts were obtained through passive lysis buffer. Luciferase activities were measured using dual luciferase reporter assay system (Promega) according to the manufacturer’s instructions. Firefly values were then normalized to Renilla values.

Statistical analysis

Statistical analysis was performed using Prism software (GraphPad Software) by either unpaired two-tail Student t-test or two-way ANOVA with Bonferroni multiple comparisons. P values of <0.05 were considered significant, with values of < 0.01 considered highly significant.