The Inhibition of the Inducible Nitric Oxide Synthase Enhances the DPSC Mineralization under LPS-Induced Inflammation

Nitric oxide (NO) is a key messenger in physiological and pathological processes in mammals. An excessive NO production is associated with pathological conditions underlying the inflammation response as a trigger. Among others, dental pulp inflammation results from the invasion of dentin by pathogenic bacteria. Vital functions of pulp mesenchymal stem cells (DPSCs, dental pulp stem cells), such as mineralization, might be affected by the inducible NOS (iNOS) upregulation. In this context, the iNOS selective inhibition can be considered an innovative therapeutic strategy to counteract inflammation and to promote the regeneration of the dentin-pulp complex. The present work aims at evaluating two acetamidines structurally related to the selective iNOS inhibitor 1400W, namely CM544 and FAB1020, in a model of LPS-stimulated primary DPSCs. Our data reveal that CM544 and even more FAB1020 are promising anti-inflammatory compounds, decreasing IL-6 secretion by enhancing CD73 expression-levels, a protein involved in innate immunity processes and thus confirming an immunomodulatory role of DPSCs. In parallel, cell mineralization potential is retained in the presence of compounds as well as VEGF secretion, and thus their angiogenetic potential. Data presented lay the ground for further investigation on the anti-inflammatory potential of acetamidines selectively targeting iNOS in a clinical context.


Introduction
The free radical nitric oxide (NO) is a ubiquitous molecular messenger which plays a key role in various physiological as well as pathological processes in mammals, bacteria, and plants. Low NO levels are generally associated with its homeostatic actions, which include immune function, control of the vascular tone and platelet aggregation, modulation of neurotransmission and memory [1]. Conversely, an excessive production of NO has been shown to be involved in immunological disorders, pain, neurological diseases, atherosclerosis, and cancer [2]. NO is endogenously synthesized by Nitric Oxide Synthases (NOSs), a family of three isoenzymes, the constitutively expressed neuronal NOS (nNOS), endothelial NOS (eNOS) and the inducible iNOS. In contrast to the constitutive NOS isoforms, the inducible produces high NO levels for sustained time periods and its activity is calcium independent. NO produced by iNOS proved to be crucial in nonspecific host defense and innate immunity, being cytotoxic against pathogen as well as tumor cells [3]. However, iNOS can promote a prolonged release of reactive nitrogen species (RNS), responsible for the damage of a wide variety of biomolecules, causing NO-related inflammatory and autoimmune diseases [4].
Dental pulp inflammation (pulpitis) results from the activation and interaction of host immune processes in response to physiochemical stimuli or both Gram-positive and Gramnegative bacteria and their toxins. The invasion of dentin by pathogenic bacteria, releasing dendritic cells and macrophages [5]. The TLR-binding starts the NF-κB (nu κB)-dependent signaling cascade which is regulated by reactive oxygen (R such as hydrogen peroxide or NO produced by the iNOS [6,7]. The product RNS species serves to induce killing or stasis of the invading microorganism cessive stimulation of NO synthesis triggered by iNOS may also lead to cy wards the host tissues, mediating the pathological effects of cytokines and pr tory enzymes [8]. Resident mesenchymal stem cells inside the dental pulp, i.e stem cells (DPSCs), are vulnerable to bacterial product-triggered infections by secreting inflammatory mediators and with dysregulated mineralizatio been recently reported that both these processes might be prone to a distur redox homeostasis, and oxidative and nitrosative stress can influence vital human dental pulp cells and their mineralization potential [10].
Based on its critical role in DPSCs, the modulation of iNOS has been p valuable strategy to prevent the irreversible damage to the dental pulp tissu mote the regeneration of dentin-pulp complex [11,12]. However, only few been published to date, which mainly investigated the effects of unselect iNOS inhibitors. Moreover, inside the dental pulp tissue, endogenous NO mainly by immunocompetent cells and dental pulp cells, and mediates not matory/immune activities, but also signaling cascades that regulate tissue r construction, indicating its involvement in both tissue destruction and regen Basically, controlled, low levels of NO derived from the constitutive NOSs eNOS, are essential under dental pulp physiological conditions, given the ro NO in angiogenesis, tissue regeneration and perfusion [7,13]. As a consequ sential not to inhibit the constitutive NOS when targeting the iNOS.
Different NOS inhibitors have been published in the last thirty years [1 of them have passed clinical trials. Therefore, there is still a need for safe mo appropriate tailored selectivity toward the inducible isoform. In this researc have previously disclosed the acetamidines CM544 and FAB1020, which a pounds structurally related to the iNOS inhibitor 1400W (Figure 1) [15,16]. T etamidines inhibit the iNOS with high potency and selectivity of action with constitutive NOSs, and, remarkably, they showed an ameliorated biological ticancer, neuroprotective and immunomodulatory agents, in comparison wit 19]. The lipophilicity of CM544 and FAB1020 also appears somewhat increa spect to the very polar and poorly cell-permeable 1400W (Table 1).    Considering the close link between inflammation and the induction of regenerative processes in the dental pulp, as well as the lack of pre-clinical data on the potential therapeutic role that selective iNOS inhibitors might play in in vitro models of pulpitis, this work aims at studying the effects played by the two promising compounds CM544 and FAB1020 in LPS-stimulated DPSCs compared to the well-known iNOS inhibitor 1400W in terms of cytotoxicity and cell responses towards inflammation. Moreover, the capability of these molecules in recovering the mineralization process and enhancing angiogenesis under inflammatory conditions was investigated.

Results and Discussion
Dental pulp cells interact with immunogenic components such as LPS (lipopolysaccharide) from deep infiltrating carious lesions, and pulp inflammation occurs. Under inflammation, the secretion of cytokines triggered by bacterial products may influence the mineralization potential of mesenchymal stem cells inside the dental pulp (DPSCs). In particular, the LPS-stimulated iNOS induction might have detrimental effects in terms of vital functions of pulp cells such as mineralization, neurogenesis, angiogenesis and neurovascular inductive activity [20], and lead to oxidative/nitrosative stress-induced cell apoptosis [6]. In this light, a selective iNOS inhibition might be beneficial to counteract inflammation in DPSCs. With this aim, a cell model of LPS-stimulated DPSCs was established and the effects of two newly synthetized selective iNOS inhibitors selected from previous investigations [17,18] were evaluated in terms of cytotoxicity, mineralization occurrence, inflammation markers and VEGF secretion. The concentrations used in the present study were chosen based on previously obtained results on human monocytes and pulp cells. In that context, all the concentrations tested were ineffective on DPSCs after 24 and 72 h, whereas doses higher than 50 µM caused cytotoxicity to human monocytes. For this reason and because compounds were here used for up to 21 days, we decided to use concentrations not higher than 50 µM [18].
To test the biocompatibility of the newly synthetized iNOS inhibitors on DPSCs, inflamed or not, a cytotoxicity assay was performed after early (3 days) and longer exposure times (21 days) and results were compared to those obtained from a 1400W exposure. After 3 days, DPSCs assessed as control (DM) weakly secrete LDH under osteogenic conditions independently from LPS (around 20% of the lysed positive control). Likewise, when the 1400W is added to cultures, LDH values are comparable to those of the control sample. In LPS-stimulated DPSCs in the presence of CM544, a significant LDH decrease is registered already at 12.5 µM and it is even more amplified at 50 µM. When the FAB1020 inhibitor is added to cultures, the LDH is slightly secreted both when the LPS is present or not. After 21 days of exposure, the LDH released in LPS-stimulated cells is doubled (64.9%) with respect to the DM alone (29.3%). The 1400W and CM544 inhibitors seem to be cytotoxic in a dose-dependent manner when cells are not stimulated with LPS, the LDH leakage assessed at 41.9% and 49.2% for both compounds at the maximum concentration of 50 µM. On the contrary, they can counteract the LPS-induced cytotoxicity, but this effect is independent of the concentration (about 48% for both compounds at all the concentration tested). On the other hand, FAB1020 significantly decreases cytotoxicity both when the LPS is present or not. More in details, a dose-dependent decrease of secreted LDH is registered up to values comparable with the DM control at 50 µM (26%) without LPS. Contrariwise, when DPSCs are LPS-stimulated, values of LDH are comparable with those in the presence of 1400W and CM544 (Figure 2). Once the biological activity of the selected iNOS inhibitors had been assessed, to investigate the occurrence of the extracellular matrix mineralization, the Alizarin Red staining was performed in all the experimental conditions after 21 days of exposure ( Figures  3A and 4A). In parallel, the expression of the stemness-related marker CD90 was assessed by immunophenotyping ( Figures 3B and 4B). The dental pulp contains mesenchymal stem cells (MSCs) which express associated markers. Remarkable expression-levels of CD90, CD73, CD105 and CD29 represent the minimal criteria for defining a multipotent mesenchymal stromal cell [21]. It has been already reported that a DPSC exposure to compounds able to act on the antioxidant molecular machinery can modulate CD marker expression and can be crucial in the MSC fate decision in terms of cell stemness loss in favor of modulation of osteogenic gene expression and mineralization occurrence [10]. In particular, the decreased expression of the GPI-anchored cell surface protein CD90 has been linked to the enhancement of the MSC osteogenic differentiation in vitro [22,23]. In our experimental model, under osteogenic conditions and in the absence of LPS ( Figure 3A), a strong increase in clusters of calcium and phosphate salts can be observed in all the experimental conditions, mainly in the presence of CM544 and even more in the presence of FAB1020 (white arrows). In parallel, expression-levels of CD90 after 3 days of culture ( Figure 3B) decrease in a dose-dependent manner in the presence of 1400W (MFI at 50 µM = 289) with respect to the DM sample (MFI = 328). The addition of CM544 to cultures already enhances the CD90 fall at 12.5 µM (MFI = 268). In the presence of FAB1020, the MFIs related to CD90 A lysed sample was set as positive lysed control (100%, not shown). DM = differentiation medium. a = p < 0.01; b = p < 0.001; c = p ≤ 0.0001 between samples and DM. d = p < 0.01; e = p < 0.001; f = p ≤ 0.0001 between samples and DM + LPS. g = p < 0.01; h = p < 0.001; i = p ≤ 0.0001 between samples and 1400W in the same experimental conditions. l = p < 0.01; n = p ≤ 0.0001 between samples and CM544 in the same experimental conditions.
Once the biological activity of the selected iNOS inhibitors had been assessed, to investigate the occurrence of the extracellular matrix mineralization, the Alizarin Red staining was performed in all the experimental conditions after 21 days of exposure ( Figures 3A and 4A). In parallel, the expression of the stemness-related marker CD90 was assessed by immunophenotyping ( Figures 3B and 4B). The dental pulp contains mesenchymal stem cells (MSCs) which express associated markers. Remarkable expression-levels of CD90, CD73, CD105 and CD29 represent the minimal criteria for defining a multipotent mesenchymal stromal cell [21]. It has been already reported that a DPSC exposure to compounds able to act on the antioxidant molecular machinery can modulate CD marker expression and can be crucial in the MSC fate decision in terms of cell stemness loss in favor of modulation of osteogenic gene expression and mineralization occurrence [10]. In particular, the decreased expression of the GPI-anchored cell surface protein CD90 has been linked to the enhancement of the MSC osteogenic differentiation in vitro [22,23]. In our experimental model, under osteogenic conditions and in the absence of LPS ( Figure 3A), a strong increase in clusters of calcium and phosphate salts can be observed in all the experimental conditions, mainly in the presence of CM544 and even more in the presence of FAB1020 (white arrows). In parallel, expression-levels of CD90 after 3 days of culture ( Figure 3B) decrease in a dose-dependent manner in the presence of 1400W (MFI at 50 µM = 289) with respect to the DM sample (MFI = 328). The addition of CM544 to cultures already enhances the CD90 fall at 12.5 µM (MFI = 268). In the presence of FAB1020, the MFIs related to CD90 are very low, independently of the inhibitor concentration, being all assessed around 200.
In the presence of a low concentration of LPS, DPSCs retain their capacity to mineralize, as shown in Figure 4A. As for their non-inflamed counterpart, clusters of calcium and phosphate salts can be observed in all the experimental conditions, mainly in the presence of CM544 and FAB1020. Expression-levels of CD90 ( Figure 4B) are also decreased dosedependently in the presence of CM544 and independently from the concentrations when the FAB1020 is present. It is therefore plausible to assume that the observations reported for LPS-stimulated DPSCs in the presence of several antioxidants [10], or rather the stimulation with a low LPS concentration, does not affect the mineralization capacity of pulp cells, are strongly validated. It has already been reported that low concentrations of NO stimulate odontogenic differentiation [24], and LPS is known to be an enhancer in NO production through NfκB activation [25]. In parallel, an exaggerated NFκB activation through massive NO generation produced through the iNOS upregulation has been reported to weaken MSC differentiation [26]. In the presence of the 1400W inhibitor, despite its selective effect on the iNOS enzyme, to less extent in the extracellular cell matrix (ECM) mineralization can be detected with respect to CM544 and FAB1020, independently from LPS. This could be related to the higher polarity of 1400W with respect to the other two compounds, as reported in Table 1, which might impair its cell permeation and thus imply a prolonged lag-time before the onset of the biological effect, as previously observed [16].
FOR PEER REVIEW 5 of 12 stimulation with a low LPS concentration, does not affect the mineralization capacity of pulp cells, are strongly validated. It has already been reported that low concentrations of NO stimulate odontogenic differentiation [24], and LPS is known to be an enhancer in NO production through NfκB activation [25]. In parallel, an exaggerated NFκB activation through massive NO generation produced through the iNOS upregulation has been reported to weaken MSC differentiation [26]. In the presence of the 1400W inhibitor, despite its selective effect on the iNOS enzyme, to less extent in the extracellular cell matrix (ECM) mineralization can be detected with respect to CM544 and FAB1020, independently from LPS. This could be related to the higher polarity of 1400W with respect to the other two compounds, as reported in Table 1, which might impair its cell permeation and thus imply a prolonged lag-time before the onset of the biological effect, as previously observed [16].   In assessing the effects of the three selective iNOS inhibitors on the DPSC min zation capacity after long exposure times (21 days), markers of inflammation were m ured earlier (3 days), to investigate whether the biological effects assessed in terms of eralization might be related to the anti-inflammatory response triggered by the sel compounds. Firstly, the IL-6 secretion was analyzed ( Figure 5A), as this interleuk gaining increasing interest owing to its dual role, both in inflammation and in od genic differentiation, highlighting the possibility of an MSC-mediated immunoregul [27]. Moreover, expression-levels of the ecto-5′nucleotidase (CD73) were measured ure 5B). Beyond its widely reported role in MSC osteoblastic/odontoblastic differenti [28], the enzymatic activity of CD73 plays a strategic role in calibrating the duration, nitude and chemical nature of purinergic signals delivered to immune cells throug conversion of ADP/ATP to AMP and AMP to adenosine, respectively [29]. It was rep that the CD73-triggered signal stimulates a shift from an ATP-driven pro-inflamm environment to an anti-inflammatory niche induced by adenosine [30]. As expected, a exposure dramatically increases the secretion of IL-6 (35.6 pg/mL) from DPSCs wit spect to the DM alone (0.3 pg/mL) in our experimental model ( Figure 5A). When inc ing concentrations of 1400W were administered, a strong dose-dependent decrease In assessing the effects of the three selective iNOS inhibitors on the DPSC mineralization capacity after long exposure times (21 days), markers of inflammation were measured earlier (3 days), to investigate whether the biological effects assessed in terms of mineralization might be related to the anti-inflammatory response triggered by the selected compounds. Firstly, the IL-6 secretion was analyzed ( Figure 5A), as this interleukin is gaining increasing interest owing to its dual role, both in inflammation and in odontogenic differentiation, highlighting the possibility of an MSC-mediated immunoregulation [27]. Moreover, expression-levels of the ecto-5 nucleotidase (CD73) were measured ( Figure 5B). Beyond its widely reported role in MSC osteoblastic/odontoblastic differentiation [28], the enzymatic activity of CD73 plays a strategic role in calibrating the duration, magnitude and chemical nature of purinergic signals delivered to immune cells through the conversion of ADP/ATP to AMP and AMP to adenosine, respectively [29]. It was reported that the CD73triggered signal stimulates a shift from an ATP-driven pro-inflammatory environment to an anti-inflammatory niche induced by adenosine [30]. As expected, a LPS exposure dramatically increases the secretion of IL-6 (35.6 pg/mL) from DPSCs with respect to the DM alone (0.3 pg/mL) in our experimental model ( Figure 5A). When increasing concentrations of 1400W were administered, a strong dose-dependent decrease of IL-6 secretion is registered (10.1 pg/mL at 50 µM). Notably, in the presence of CM544 and FAB1020, IL-6 secretion is already slightly detected at 12.5 µM (10.1 pg/mL and 8.2 pg/mL, respectively). In parallel, CD73 is upregulated in all the experimental conditions with respect to DM (MFI = 143.6) and LPS alone (MFI = 115.2). In more detail, in the presence of 1400W and LPS, MFIs related to CD73 are significantly higher than those of the control sample (MFI at 25 µM = 167.1) but to a lesser extent than in the presence of CM544 and FAB1020 (MFIs at 25 µM = 272.4 and 291.2, respectively). It is therefore plausible to speculate that the decrease in IL-6 secretion under LPS-induced pro-inflammatory conditions might be triggered by the CD73, its expression-levels being increased when the IL-6 is weakly secreted. Moreover, this intriguing observation seems to confirm the proposed role in immunomodulation for DPSCs and in general for MSCs. R PEER REVIEW 7 of 12 speculate that the decrease in IL-6 secretion under LPS-induced pro-inflammatory conditions might be triggered by the CD73, its expression-levels being increased when the IL-6 is weakly secreted. Moreover, this intriguing observation seems to confirm the proposed role in immunomodulation for DPSCs and in general for MSCs. DPSCs exist in the vessel microenvironment in vivo and have a close association with endothelial cells. It has been reported that these cells have a mutual effect on each other, because MSC-induced promotion of tooth regeneration is highly associated with increased angiogenesis, which promotes cell migration and growth factor delivery to the injured site [31,32]. Against this background the secretion of VEGF was measured in all the experimental conditions ( Figure 6). In vivo transplantation studies have shown that silencing VEGFR-2 hampers odontoblastic differentiation of DPSCs [33]. Hardly detectable, and thus insignificant, fluctuations can be observed in the presence of 1400W and CM544 with respect to the control samples, independently from LPS. On the contrary, FAB1020 slightly but significantly increases VEGF secretion, mainly in the presence of LPS. These findings are in line with the well-known role of NO in both physiological and pathological angiogenesis [34] and with the fact that a correct modulation of NO production, due to a regulated balance among the three-isoform activity, is necessary for physiological osteogenesis [35]. . c = p ≤ 0.0001 between samples and DM. f = p ≤ 0.0001 between samples and DM + LPS. g = p < 0.01; h = p < 0.001; i = p ≤ 0.0001 between samples and 1400W in the same experimental conditions. l = p < 0.01; n = p ≤ 0.0001 between samples and CM544 in the same experimental conditions. DPSCs exist in the vessel microenvironment in vivo and have a close association with endothelial cells. It has been reported that these cells have a mutual effect on each other, because MSC-induced promotion of tooth regeneration is highly associated with increased angiogenesis, which promotes cell migration and growth factor delivery to the injured site [31,32]. Against this background the secretion of VEGF was measured in all the experimental conditions ( Figure 6). In vivo transplantation studies have shown that silencing VEGFR-2 hampers odontoblastic differentiation of DPSCs [33]. Hardly detectable, and thus insignificant, fluctuations can be observed in the presence of 1400W and CM544 with respect to the control samples, independently from LPS. On the contrary, FAB1020 slightly but significantly increases VEGF secretion, mainly in the presence of LPS. These findings are in line with the well-known role of NO in both physiological and pathological angiogenesis [34] and with the fact that a correct modulation of NO production, due to a regulated balance among the three-isoform activity, is necessary for physiological osteogenesis [35].

Synthesis of iNOS Inhibitors
The two selective iNOS inhibitors CM544 and FAB1020 were synthesized, pu and characterized as previously reported [15,16]. 1400W was purchased from (Darmstadt, Germany). Compounds were stored at −20 °C.

Establishment of Pro-Inflammatory Conditions and Cell Exposures to Inhibitors
DPSCs from routine culture were seeded as passage 6 in complete α-MEM an bated for 48 h at 37 °C and 5% CO2. After that, cells were stimulated by Lipopolys ride (LPS from E. coli, Merck, Darmstadt, Germany) 0.1 µg/mL to establish an in environment. In parallel, DPSCs were exposed to the iNOS inhibitors 1400W or C (stock solutions 50 mM in deionized water) or FAB1020 (stock solution 50 mM in D at 12.5, 25 and 50 µM, with or without LPS. All the exposures were performed odontogenic conditions by diluting the LPS and compounds in complete α-MEM s mented with 10 nM dexamethasone, 10 mM β-glycerophosphate and 50 µg/mL a acid (all from Merck, Darmstadt, Germany) as described elsewhere [10]. Fresh ex media were provided every 72 h.

Lactate Dehydrogenase (LDH) Release
Cells from routine culture were seeded (7 × 10 3 /well; 96-well plates) in 200 µL tine culture medium (complete α-MEM) and incubated for 48 h at 37 °C and 5% CO cells were treated as described previously in this section for up to 21 days. To qu cytotoxicity after 3 and 21 days, supernatants were harvested, kept on ice, and the

Synthesis of iNOS Inhibitors
The two selective iNOS inhibitors CM544 and FAB1020 were synthesized, purified, and characterized as previously reported [15,16]. 1400W was purchased from Merck (Darmstadt, Germany). Compounds were stored at −20 • C.

Establishment of Pro-Inflammatory Conditions and Cell Exposures to Inhibitors
DPSCs from routine culture were seeded as passage 6 in complete α-MEM and incubated for 48 h at 37 • C and 5% CO 2 . After that, cells were stimulated by Lipopolysaccharide (LPS from E. coli, Merck, Darmstadt, Germany) 0.1 µg/mL to establish an inflamed environment. In parallel, DPSCs were exposed to the iNOS inhibitors 1400W or CM544 (stock solutions 50 mM in deionized water) or FAB1020 (stock solution 50 mM in DMSO) at 12.5, 25 and 50 µM, with or without LPS. All the exposures were performed under odontogenic conditions by diluting the LPS and compounds in complete α-MEM supplemented with 10 nM dexamethasone, 10 mM β-glycerophosphate and 50 µg/mL ascorbic acid (all from Merck, Darmstadt, Germany) as described elsewhere [10]. Fresh exposure media were provided every 72 h.

Lactate Dehydrogenase (LDH) Release
Cells from routine culture were seeded (7 × 10 3 /well; 96-well plates) in 200 µL of routine culture medium (complete α-MEM) and incubated for 48 h at 37 • C and 5% CO 2 . Next, cells were treated as described previously in this section for up to 21 days. To quantify cytotoxicity after 3 and 21 days, supernatants were harvested, kept on ice, and the CytoTox 96 ® Non-Radioactive Assay (Promega Corporation, Fitchburg, WI, USA) was performed as already reported [36]. The assay quantitatively measures LDH, a stable cytosolic enzyme that is released upon cell lysis. The maximum LDH release control (positive control) was obtained by adding a lysis solution in a well containing untreated DPSCs and processing the obtained supernatant as for the other experimental conditions. The optical density (O.D.) was measured at 490 and 690 nm by means of a multiscan GO microplate spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA) and the obtained O.D. were normalized with that related to the positive control (lysed cells). Assessment of cytotoxicity was calculated according to the formula: %LDH released = [(A − B)/(C − B)] × 100, with A = LDH activity of sample, B = LDH activity of untreated cells and C = LDH activity of the positive lysed control.

Interleukin-6 Release
Absolute amounts of IL-6 (pg/mL) were quantified in cell culture supernatants from the same wells used for the LDH assay after 3 days of exposure using a commercial ELISA kit (Enzo Life Sciences Inc, Lausen, Switzerland) as reported previously [18]. Cytokine concentrations were calculated from standard curves using the Prism5 software 5.0 (GraphPad, San Diego, CA, USA). Individual values obtained from independent experiments (n = 4) were summarized as means and standard deviations.

Immunophenotype In Vitro by Flow Cytometry
The expression of surface markers in DPSCs was analyzed by flow cytometry. Cells from routine cultures were seeded (5 × 10 4 /well) in 3 mL of complete α-MEM medium in 6-well plates and then they were let to adhere for 48 h. After exposures for 3 days, cells were harvested and incubated with fluorochrome-conjugated antibodies (1:50 dilutions), namely anti-human cluster of differentiation (CD)90-FITC (BD Biosciences, San Diego, CA, USA) and CD73-PE (R & D Systems, Minneapolis, MN, USA) monoclonal antibodies as reported previously [23]. Relative fluorescence emissions of gated cells by forward and side scatter properties (FSC/SSC) were analyzed with the CytExpert software 2.3 (Beckman Coulter, CA, USA) and expressed as mean fluorescence intensities (MFIs). Individual values obtained from independent experiments (n = 6) were summarized as means and standard deviations.

Extracellular Matrix Mineralization (Alizarin Red Staining)
Cells from routine culture were seeded (5 × 10 4 /well) in 3 mL of complete α-MEM medium in 6-well plates and then let to adhere for 48 h. Then, the cultures were treated as described above. The exposure of cultures was stopped after 21 days by discarding the exposure media. Then, the calcium precipitation was detected after Alizarin red staining of cell cultures following an established procedure [37].

ELISA Analysis of VEGF Secretion
After 21 days of treatment, cell supernatants were collected from the 6-well plate used for the alizarin red staining. The VEGF ELISA kit (Enzo Life Sciences, Farmingdale, NY, USA) was used to perform a quantitative determination (pg/mL) of human VEGF released in the medium following the manufacturer's instructions. VEGF values were obtained by using a standard curve generated with specific standards, provided by the manufacturer. Individual values obtained from independent experiments (n = 4) were summarized as means and standard deviations.

Statistics
Statistical analysis was performed using the GraphPad 5.0 software (GraphPad Software, San Diego, CA, USA), by means of a t-test and ordinary one-way ANOVA, followed by post hoc Tukey's multiple comparisons tests. Values of p < 0.05 were considered statistically significant.

Conclusions
The present work investigates the effects of two newly synthetized selective iNOS inhibitors, namely CM544 and FAB1020, in a cell model of human DPSCs stimulated by LPS to induce an inflamed environment. Our results were compared to those obtained in the presence of 1400W, a known selective iNOS inhibitor. The investigation context is intriguing, considering the close link between inflammation and the induction of regenerative processes in the dental pulp. In parallel, this investigation is innovative, due to the lack of pre-clinical data on the potential therapeutic role that selective iNOS inhibitors might play in in vitro models of pulpitis. Our results reveal that CM544, and even more FAB1020, are effective in decreasing the inflammatory response in DPSCs, by impairing IL-6 secretion and upregulating the MSC marker CD73, an ecto-5 nucleotidase which also has several key functions in cell responses towards inflammation, associated with the shift from an ATP-driven pro-inflammatory environment to an anti-inflammatory niche induced by adenosine. In parallel, the ECM mineralization is retained and further increased in the presence of the two inhibitors, with respect to 1400 W. Data reported confirm the effectiveness of CM544 and FAB1020 and their ameliorated biological profile with respect to 1400 W. Moreover, by exposing cells to these compounds, knowledge of the biology of DPSCs has been improved, confirming their active role not only in odontogenesis but also in immunomodulation and cell responses towards inflammation. This study lays the ground for future investigations about the role of NO in the dental pulp complex and in cells at the dentin-pulp interface. Moreover, the function of MSCs in the dental pulp as cells modulating immunity under pathogenic stimuli or stressor exposition is worthy of investigation in detail. Based on their effectiveness in the present experimental model, the iNOS selective inhibitors here tested could be studied in cell models of regeneration or in a tissue engineering context.