Abstract Inducible nitric oxide synthase (iNOS) is a major source of nitric oxide during inflammation whose activity is thought to be controlled primarily at the expression level. The B1 kinin receptor (B1R) post-translationally activates iNOS beyond its basal activity via extracellular signal regulated kinase (ERK)-mediated phosphorylation of Ser 745. Here we identified the signalling pathway causing iNOS activation in cytokine-treated endothelial cells or HEK293 cells transfected with iNOS and B1R. To allow kinetic measurements of nitric oxide release, we used a sensitive porphyrinic microsensor (response time = 10 msec.; 1 nM detection limit).
B1Rs signalled through G i coupling as ERK and iNOS activation were inhibited by pertussis toxin. Furthermore, transfection of constitutively active mutant G i Q204L but not G q Q209L resulted in high basal iNOS-derived nitric oxide. G-β subunits were also necessary as transfection with the β-adrenergic receptor kinase C-terminus inhibited the response.
B1R-dependent iNOS activation was also inhibited by Src family kinase inhibitor PP2 and trans-fection with dominant negative Src. Other ERK-MAP kinase members were involved as the response was inhibited by dominant negative H-Ras, Raf kinase inhibitor, ERK activation inhibitor and MEK inhibitor PD98059. In contrast, PI3 kinase inhibitor LY94002, calcium chelator 1,2-bis-(o-Aminophenoxy)-ethane-N,N,N′,N′-tetraacetic acid, tetraacetoxymethyl ester (BAPTA-AM), protein kinase C inhibitor calphostin C and protein kinase C activator PMA had no effect. Angiotensin converting enzyme inhibitor enalaprilat also directly activated B1Rs to generate high output nitric oxide via the same pathway. These studies reveal a new mechanism for generating receptor-regulated high output nitric oxide in inflamed endothelium that may play an important role in the development of vascular inflammation. • • Introduction Nitric oxide regulates diverse physiological and pathological responses in the cardiovascular system [].
A novel pathway for receptor-mediated post-translational activation of inducible nitric oxide synthase. B1Rs signalled through G i coupling as ERK. Epigenetic regulation of nitric oxide synthase 2, inducible (Nos2) by NLRC4 inflammasomes involves PARP1 cleavage. Carina de Lima Buzzo;, Tiago Medina;, Laura M. A novel pathway for inducible nitric-oxide synthase activation through inflammasomes. The Journal of biological chemistry 285,. In this study, the anti-inflammatory effects and mechanisms of baicalin on LPS-induced NLRP3 inflammatory pathway were investigated. Baicalin, anti-inflammation, NLRP3 inflammasome, piglet peripheral blood mononuclear cell, reactive oxygen species. And inducible nitric oxide synthase (iNOS), and the syn- thesis of. Jan 30, 2017 Nos2 nitric oxide synthase 2, inducible. Nlrc4 inflammasomes and illustrated a novel. Activation of inducible nitric-oxide synthase and. A novel pathway for receptor-mediated post-translational activation of inducible nitric. Inducible nitric oxide synthase. Oxide through the B1R-Gαi-MAPK pathway.
Three distinct isoforms of nitric oxide synthase (NOS) produce nitric oxide from the precursor amino acid L-Arg. The constitutively expressed endothelial and neuronal NOS (eNOS and nNOS) have low basal activity that is enhanced by receptor stimulation leading to increased intracellular calcium, phosphorylation at key residues and/or altered interactions with regulatory proteins []. In contrast, inducible NOS (iNOS) is not constitutively expressed in most cells and the regulation of its activity is considered to be primarily at the level of transcription and expression in response to cytokines and inflammatory mediators []. Furthermore, iNOS contains tightly bound Ca ++/calmodulin that does not dissociate in resting cells, and it is constitutively active once synthesized [].
This has lead to the prevailing view that iNOS generates unregulated high output nitric oxide (given sufficient substrate and cofactors) until the protein is degraded []. Recent studies have suggested some mechanisms for post-translational regulation of iNOS that affect basal activity or protein expression. For example, iNOS dimerization and activity are inhibited by S-nitrosylation [] and interaction with kalirin or NAP110 [] but enhanced by interaction with hsp90 []. INOS activity is also reduced by sequestration in aggresomes [], and its degradation is enhanced by interaction with caveolin-1[].
The phosphorylation sites that are important in regulating eNOS activity [] are not conserved in iNOS and its regulation by phosphorylation has not been well studied. Recently it was reported that co-transfection of iNOS and activated Src results in increased phosphorylation of iNOS at Tyr 151 and decreased activity [] and phosphorylation of iNOS at Y 1055 by Src results in increased iNOS half-life []. We found that activation of kinin B1 receptors (B1Rs) by peptide agonist or angiotensin converting enzyme (ACE) inhibitors led to generation of iNOS-derived high output nitric oxide in cytokine-pretreated human lung microvascular endothelial cells (HLMVEC) [], suggesting a novel mode of acute post-translational regulation of iNOS that fundamentally differs from known mechanisms. Indeed, we discovered that B1R stimulation activated the extracellular signal-regulated kinase (ERK) which phosphorylated iNOS on Ser 745, leading to a 2.5 to 5-fold further increase in nitric oxide production over basal activity []. More recently, platelets were found to constitutively express iNOS and platelet agonists at low doses ( e.g. Thrombin) acutely stimulated iNOS-mediated nitric oxide production to enhance platelet secretion and aggregation []. These findings indicate a novel mode of acute activation of iNOS via G protein coupled receptor (GPCR)-mediated signalling pathways that are still to be delineated.
We undertook the present study to investigate the upstream signal transduction pathway and mitogen activated protein kinase (MAPK) components activated by B1R stimulation that leads to post-translational activation of iNOS-dependent high-output nitric oxide. Here we show that B1R-mediated activation of iNOS requires G i and β -dependent activation of Src, Raf, Ras, MAPK/ERK kinase (MEK) and ERK. This newly described signalling pathway for high output nitric oxide production may play an important role in the development of vascular inflammation. Materials and methods Materials Reagents were obtained from Sigma (St. Louis, MO, USA) unless otherwise stated. Low-glucose Dulbecco's modified Eagle's medium (DMEM) without phenol red and custom-made L-Arg-free DMEM were from Invitrogen (Carlsbad, CA, USA).
5-Iodo-3-[(3,5-dibromo-4-hydroxyphenyl)methylene]-2-indolinone (Raf kinase inhibitor), Ste-MPKKKPTPIQLNP-NH2 (ERK activation inhibitor peptide I), 2′-Amino-3′-methoxyflavone (PD 98059), 4-amino-5-(4-chlorophenyl)-7-( t-butyl)pyrazolo[3,4- d]pyrimidine (PP2), SH-6, and myr-SIRKALNILGYPDYD-OH (m-SIRK) were obtained from Calbiochem (San Diego, CA, USA). Enalaprilat, the active form of the ACE inhibitor enalapril, was from Merck. Human iNOS cDNA in pcDNA3 was a gift from Dr.
Timothy Billiar, Univ. Of Pittsburgh. Human B1R cDNA was a gift from Dr. Fredrik Leeb-Lundberg, Univ.
Of Lund, Sweden. Adenoviral vector (type 5) encoding the C-terminus of β-adrenergic receptor kinase 1 (Adv-ct-βARK) or empty vector control (Adv-EV) were generous gifts from Dr. Koch (Jefferson Medical College, Philadelphia, PA, USA). Dominant-negative (DN) Src (Y527F, K295M) in vector pSM was a gift from Dr. Silvio Gutkind (National Institute of Dental Research, National Institutes of Health, Bethesda, MD, USA), G i Q205L, G q Q209L and DN-H-Ras (S17N), were from Missouri University of Science and Technology cDNA Resource Center (Rolla, MO, USA). Antibodies to ERK and phospho-ERK were from New England Biolabs (Ipswich, MA, USA).
Antibodies to human iNOS, G q and eNOS were from BD Transduction Laboratories (San Jose, CA, USA) and anti-G i antibody was from Calbiochem (San Diego, CA, USA). Antibodies for β-actin and GAPDH were from Ambion (Austin, TX, USA). Cell culture and transfections HLMVEC (Cambrex, East Rutherford, NJ, USA) were cultured in EBM-2 medium with growth factors from EGM-2 Bullet kits (CC-3162, Lonza, Rockland, ME, USA) and 10% fetal bovine serum (FBS). HLMVEC were used from passages 5 to 8 (at 85–100% confluence), and were pre-treated with 5 ng/ml interleukin-1β (IL-1β) and 100 U/ml interferon- (IFN- ) for 16 to 18 hrs to induce expression of B1Rs and iNOS. HEK293 cells were maintained in DMEM containing 10% FBS, 100 μg/ml streptomycin and 100 U/ml penicillin.
Transfections of HLMVEC with B1R, iNOS, G i Q204L, G q Q209L, DN-H-RAS, or DN-Src were done using an Amaxa Nucleofector (Amaxa, Walkersville, MD, USA) with the manufacturer's optimized buffer kit and protocol (S005) for HLMVEC. HEK293 cells were transfected with iNOS, B1R, G i Q204L mutant, G q Q209L mutant, DN-H-Ras or empty plasmids with Effectene transfection reagent per manufacturer's instructions. After 24 hrs, cells were washed and maintained in DMEM/F-12 with 0.5% FBS overnight and then changed to the medium indicated for experiments. HLMVEC or HEK cells were infected with the adenovirus empty vector control (Adv-EV) or Adv-ct-βARK for 36 hrs in medium containing 10% FBS and then serum-deprived for 12 hrs before experiments []. Measurement of nitric oxide production For direct measurement of nitric oxide generation in real time, a porphyrinic microsensor was used as described []. The microsensor is highly sensitive for nitric oxide, and its response time is rapid, providing the ability to make kinetic measurements of nitric oxide generation.
The porphyrinic sensor was positioned with a micromanipulator close to the cell culture surface (20 ± 1 μm). To measure L-Arg-dependent basal iNOS-mediated nitric oxide generation, cells were incubated for 2 hrs in L-Arg-free media and then 1 mM L-Arg was added and the response (current versus time) recorded continuously. To initiate B1R-dependent iNOS activation and nitric oxide production, cells were incubated in L-Arg-containing media and then 100 nM des-Arg 10-kallidin (DAKD) or 100 nM ACE inhibitor enalaprilat were added to initiate the response. Current generated was proportional to the nitric oxide released, and a computer-based Gamry VP600 potentiostat was used to monitor nitric oxide concentration over time.
Each electrode was calibrated with a nitric oxide standard. The concentration of nitric oxide achieved 20 min. After addition of agonist or substrate was used to quantitate the results. Immunoblotting Cells were washed with ice-cold PBS, collected and lysed for 30 min.
On ice in lysis buffer (25 mM Tris pH 7.5, 150 mM NaCl, 5 mM ethylenedi-aminetetraacetic acid, 10% glycerol, 1% NP-40, 1%[v/v] protease inhibitor cocktail [Sigma] and 1 mM phenylmethylsulfonyl fluoride (PMSF)) and then centrifuged at 16,000 × g for 15 min. The resulting super-natant was resolved by SDS-PAGE on 8–16% gradient gels (ISC BioExpress) transferred to polyvinylidenefluoride (PVDF) membranes and detected with appropriate primary antibodies followed by horseradish per-oxidase-labelled second antibody (Pierce, Rockford, IL, USA) and enhanced chemiluminescence (SuperSignal West Femto Maximum Sensitivity Substrate, Thermo Scientific, Waltham, MA, USA). Detection of ERK activation HLMVEC or HEK293 cells were serum-starved in DMEM/F12 for 3 hrs to decrease basal ERK phosphorylation and allow more sensitive detection of B1R-dependent activation.
Cells were then treated with 100 nM DAKD as indicated, washed twice with ice-cold PBS containing 100 μM sodium orthovanadate, collected by centrifugation and then lysed as above with lysis buffer also containing 20 mM p-nitrophenylphosphate, 25 mM NaF, 20 mM β-glycerolphosphate and 1 mM sodium orthovanadate to inhibit phosphatases. Samples were centrifuged (16,000 × g, 4°C, 15 min.) and the supernatants used. For detection of ERK, aliquots were added to an equal volume of 2 SDS-PAGE sample buffer, boiled for 5 min. And subjected to Western blotting with antibody to total or phospho-ERK (New England Biolabs). Statistical analysis Data are expressed as the mean ± S.E. Statistical analysis was performed with the two-way anova and Newman–Keuls test for multiple comparisons.
The value of P. • • B1R agonist stimulates iNOS-dependent high output nitric oxide in cytokine-treated HLMVEC. ( A) Control HLMVEC were pre-incubated for 2 hrs in L-Arg-free medium ( top) or maintained in medium containing 1 mM Arg ( bottom) and then 1 mM Arg ( top) or 100 nM DAKD ( bottom) was added and real-time nitric oxide was measured with a porphyrinic microsensor for 80 min. ( B) HLMVEC were treated with cytokines for 16 hrs to induce iNOS and B1R expression. Cells were either pre-incubated for 2 hrs in L-Arg-free medium ( dashed lines) or maintained in medium containing 1 mM Arg ( solid lines).
Where indicated, cells were also pre-incubated for 20 min. With either B1R antagonist DALKD (1 μM) or iNOS inhibitor 1400 W (4 μM).
To stimulate basal or B1R-dependent nitric oxide production, 1 mM Arg or 100 nM DAKD was added and real-time nitric oxide was measured with a porphyrinic microsensor for 80 min. ( C) HLMVEC were pretreated with cytokines and pre-incubated in L-Arg-free medium for 2 hrs.
Some cells were pre-treated for 20 min. With 25 μM BAPTA-AM, 1 μM DALKD or 4 μM 1400 W min. As indicated. 1 mM L-Arg was added first to activate basal iNOS-mediated nitric oxide, followed 5 min.
Later by 100 nM DAKD to stimulate B1R-dependent activation of iNOS (except tracing labelled ‘L-Arg alone’). ( D) Immunoblotting of iNOS in lysates of control or cytokine-treated HLMVEC. Data are representative of three experiments.
Cytokines up-regulate the expression of iNOS and B1Rs []. HLMVEC were treated with IL-1β (5 ng/ml) and IFN- (100 U/ml) for 16–18 hrs and then in L-Arg-free medium for 2 hrs to reduce basal iNOS activity. In these cytokine-treated HLMVEC, 1 mM L-Arg produced a much higher basal output of nitric oxide (200 ± 15 nM; n= 10) than in control cells. This was due to iNOS as it was inhibited by the specific inhibitor 1400 W (), consistent with an increase in iNOS expression in cytokine-treated HLMVEC (). B1R agonist DAKD, added to cells pre-incubated in L-Arg-containing medium, caused a greater increase in nitric oxide output (maximum = 355 ± 25 nM; n= 10) compared with Arg-stimulated basal activity (). This activity was inhibited by the specific B1R antagonist des-Arg 10-Leu 9-kallidin (DALKD) (). Cells stimulated with DAKD in the absence of L-Arg did not produce detectable nitric oxide (), consistent with reports showing iNOS activity is dependent on extracellular Arg [].
To further demonstrate the receptor-mediated acute activation of iNOS, cytokine-treated HLMVEC were depleted of Arg for 2 hrs, then 1 mM L-Arg was added to generate basal iNOS activity (). Addition of 100 nM DAKD 5 min.
After adding L-Arg resulted in an increase in the rate of nitric oxide release that was blocked by B1R antagonist DALKD (). The intracellular Ca ++-chelating agent BAPTA-AM had no effect on L-Arg or B1R-mediated nitric oxide production (), consistent with the independence of iNOS activity on increased intracellular Ca ++[].
Pre-treatment of HLMVEC with iNOS specific inhibitor 1400 W inhibited basal and receptor-stimulated nitric oxide output whereas B1R antagonist DALKD (1 μM) inhibited only the latter (). We previously found that B1R-dependent nitric oxide production in HLMVEC was not due to eNOS activation [] as eNOS inhibitor L-N G-nitroarginine at 4 μM concentration (which has no effect on iNOS in control studies) did not inhibit B1R-mediated nitric oxide production. Furthermore, control HLMVEC (which constitutively express eNOS) transfected with only the B1R, did not generate significant nitric oxide when stimulated with B1R agonist []. To further prove this point, we measured eNOS expression and activity in response to cytokine treatment. As shown in, eNOS protein is readily detected in control HLMVEC, but its expression did not change after cytokine treatment.
Furthermore, stimulation of eNOS activity with calcium ionophore A23187 resulted in a short burst of nitric oxide production that returned to baseline in 1 min. And did not increase after cytokine treatment (). Finally, nNOS protein was undetectable by Western analysis in control or cytokine-treated HLMVEC and nitric oxide production was unaffected by a specific nNOS inhibitor (not shown). Taken together, the above data show that B1R-dependent nitric oxide production in cytokine-treated HLMVEC is due to activation of iNOS.
• • eNOS expression and Ca 2+-dependent activation are not affected by cytokine treatment. ( A) Control or cytokine-treated HLMVEC were lysed and eNOS expression was assessed by Western analysis using eNOS-specific monoclonal antibody. Results are representative of two experiments done in duplicate. ( B) Ca 2+-dependent eNOS activity was stimulated in control or cytokine-treated HLMVEC by adding 10 μM calcium ionophore A23187 at time 0 and nitric oxide generation was measured with a por-phyrinic electrode. Tracings shown are representative of 4 experiments. ( C) Quantitation of maximal nitric oxide concentration achieved in experiments described in B.
Results shown are mean ± S.E.M for n= 4. To further prove that B1Rs can activate iNOS, their cDNAs were transfected into control HLMVEC or HEK293 cells. Transfection of iNOS and B1Rs into HLMVEC increased basal, L-Arg-dependent nitric oxide production equivalent to that in cytokine-treated HLMVEC whereas B1R-stimulated nitric oxide production was even higher in transfected HLMVEC than after cytokine treatment (). Mock transfection did not change B1R-dependent nitric oxide production in cytokine-treated HLMVEC (). • • Basal and B1R-activated nitric oxide release in cytokine treated HLMVEC or in HEK cells or HLMVEC transfected with B1R and iNOS. ( A) HLMVEC were pre-treated with cytokines to induce iNOS and B1R expression or electroporated with iNOS and B1R cDNAs as described in ‘Materials and methods’.
Basal Arg-dependent nitric oxide generation was measured by incubating cells for 2 hrs in L-Arg-free media and then adding 1 mM L-Arg to initiate the response. To measure B1R-dependent iNOS activation and nitric oxide production, cells were maintained in L-Arg-containing media and B1R agonist (100 nM DAKD) was added to stimulate the response.
In both cases, nitric oxide production was measured continuously with a porphyrinic electrode, and the nitric oxide concentration achieved at 20 min. Used to quantitate the results. Results shown are mean values ± S.E.M for n= 3. • • B1R-mediated iNOS activation is PTX sensitive. HLMVEC were pre-treated with cytokines and HEK293 cells were transfected with iNOS and B1R as described in ‘Materials and methods’.
Cells were pre-treated with PTX (1.5 μg/ml) for 3 hrs. Basal Arg-mediated ( A) or B1R-activated ( B) iNOS-dependent nitric oxide production was measured as described (see legend and ‘Materials and methods’). Data shown are mean values ± S.E.M for n= 3. • • Effect of transfection with constitutively active G i, ct-βARK or dominant-negative Src on iNOS-dependent nitric oxide production.
( A) Representative tracings of real time nitric oxide measurement. HLMVEC were trans-fected with G i Q204L ( top) or G q Q209L ( bottom) and treated with cytokines. Basal Arg-mediated or B1R-activated iNOS-dependent nitric oxide production was measured as above (see legend and ‘Materials and methods’). ( B) HLMVEC or HEK293 cells were transfected with B1R, iNOS, and G i Q204L or G q Q209L and basal Arg-mediated or B1R-activated iNOS-dependent nitric oxide production was measured as above. Data shown are mean values ± S.E.M for n= 3; * P.
• • B1R agonist-induced iNOS activation is dependent on Ras, Raf and Erk. ( A) HLMVEC were cytokine treated as before and HEK293 cells were trans-fected with iNOS + B1R. Some cells were transfected with DN-H-Ras or pretreated with Raf kinase inhibitor (100 nM, 20 min.) or Src family kinase inhibitor PP2 (15 μM, 30 min.). In all samples, B1R-dependent nitric oxide release was measured in response to 100 nM DAKD as described (see legend and ‘Materials and methods’). ( B) HLMVEC were cytokine treated and HEK293 cells were transfected with iNOS + B1R. Cells were pre-treated with ERK activation inhibitor (10 μM, 20 min.) or MEK inhibitor PD98059 (50 μM, 30 min.). Basal Arg-dependent or B1R-activated nitric oxide release were measured as above (see legend and ‘Materials and methods’).
( C) Cytokine-treated HLMVEC or HEK293 cells transfected with iNOS + B1R were pre-treated with PI3K inhibitor LY94002 (10 μM, 30 min.), PKC activator PMA (1 μM, 30 min.), PKC inhibitor calphostin C (1 μM, 30 min.) or Akt inhibitor SH6 (25 μM, 30 min.) and B1R-dependent nitric oxide release in response to 100 nM DAKD was measured as above. ( D) HEK293 cells were transfected with iNOS, B1R, and constitutively active mutants G i Q204L or G q Q209L. Some cells were pre-treated with MEK inhibitor PD98059 (50 μM, 30 min.) and Arg-dependent nitric oxide release was measured as above. Data shown are mean values ± S.E.M for n= 3. • • B1R-mediated ERK activation depends on G i, Src and MEK. ( A) Representative Western blots of phospho- ERK (p-ERK) in cytokine-treated HLMVEC which were pre-incubated without or with PP2 (15 μM, 30 min.), PTX (1.5 μg/ml, 3 hrs), m-SIRK (1 μM, 30 min.), or PD98059 (50 μM, 30 min.) and stimulated with 100 nM DAKD for the indicated time.
Cells were lysed and analyzed by Western blotting with polyclonal antibody to phospho- ERK. Blots were stripped and re-probed with monoclonal antibody to β-actin or total ERK as protein loading controls. ( B) Graph shows quantitation of Western blots by densitometry, normalized for protein loading (β-actin or total ERK staining).
Bars indicate mean ± S.E.M. ( n= 3 each).
• • ACE inhibitor generates iNOS-dependent high output nitric oxide through the B1R-G i-MAPK pathway. HLMVEC were pre-treated with cytokines and pre-incubated with or without B1R antagonist DALKD (1 μM, 30 min.), B2R antagonist HOE140 (1 μM, 30 min.), PTX (1.75 μg/ml, 3 hrs), PD98059 (50 μM, 30 min.) or 1400 W (4 μM, 30 min.).
B1R peptide agonist DAKD (100 nM) or ACE inhibitor enalaprilat (100 nM) were added and nitric oxide production was recorded continuously for 20 min. Data show mean values ± S.E.M for n= 3.
• • Schematic diagram of the signalling pathway activated by B1R agonists leading to iNOS-derived high output nitric oxide. Expression of iNOS and the B1R are induced under inflammatory conditions. INOS has constitutive activity, which can be further enhanced by B1R agonists DABK, DAKD or ACE inhibitors via B1R-dependent activation of the ERK/MAP kinase pathway as shown. This results in phosphorylation of iNOS at Ser 745, leading to generation of high output nitric oxide in endothelial cells. Activation of MAPKs by GPCRs can occur through several pathways, including those coupled through G i or G q/11 []. B2Rs couple through G q/11 and/or G i to activate MAPKs via several pathways (depending on cell type), but PKC activation is usually required [].
Effective B2R activation of ERK in trans-fected HEK cells required the cooperative signalling of both G i-mediated Ras activation and G q-mediated stimulation of PLCβ→PKC→Raf []. In contrast, our results suggest that B1R activation of ERK is independent of G q, Ca 2− and PKC but instead requires both G i and β (). Activation of ERK by G i is usually mediated through the release of β subunits and activation of Src, consistent with our results. However, the constitutively active G i Q204L mutant stimulated high output nitric oxide in our studies, indicating an additional role for direct ERK activation through the G i subunit.
Although the mechanism is unknown, it has been reported that G i can directly activate Ras or stimulate the ERK MAPK pathway indirectly by activating Rap1GAPII to relieve Rap1 inhibition of C-Raf or by inhibiting adenylyl cyclase and cAMP formation to reduce PKA-mediated inhibition of C-Raf []. GPCR activation of ERK can also occur via transactivation of the EGF receptor []. However, in other studies we have shown that B1R activation does not transactivate the EGF receptor and that EGF-mediated ERK activation does not lead to activation of iNOS-derived nitric oxide production (Kuhr FK, Zhang Y, Brovkovych V and Skidgel RA, unpublished). MAPK activation usually results in its translocation to the nucleus to regulate transcription. However, B1R-mediated activation of iNOS would require retention of activated ERK in the cytosol where it can phosphorylate iNOS.
GPCR-dependent ERK activation can be mediated by β-arrestin, which scaffolds members of the MAPK pathway to enhance efficiency of activation, resulting in a slower and more sustained activation and retention of active ERK in the cytosol []. Consistent with this model, we recently found that sustained, B1R-dependent ERK and iNOS activation is β-arrestin 2 dependent (Kuhr FK, Zhang Y, Brovkovych V, Skidgel RA, unpublished). B1R and iNOS expression are both induced by inflammatory mediators as is the expression of carboxypeptidase M, the membrane enzyme critical for generating and delivering B1R agonist to the receptor []. Thus, the B1R–iNOS pathway may play important roles in inflammation where B1R signalling can have both deleterious and beneficial effects []. For example, B1R knockout protected mice from LPS-induced hypotension, reduced pain in response to thermal or chemical stimuli as well as neuropathic pain, and reduced intestinal ischemia/reperfusion injury and lethality []. However, B1R signalling is also beneficial, for example in protecting kidneys from ischemia/reperfusion injury [], promoting vasodilation, angiogenesis and neovascularization during wound healing [], and reducing lethality in a porcine model of endotoxic shock []. The B1R may also participate in the protective effects of ACE inhibitors in heart disease and diabetes [].
One way ACE inhibitors might do this is by acting as direct agonists of the B1R as reported previously []. ACE inhibitor stimulation of B1Rs depends on a consensus HEXXH zinc binding motif in the second extracellular loop that is not required for peptide agonist binding or activation []. In bovine pulmonary artery endothelial cells that constitutively express B1Rs, ACE inhibitor enalaprilat and B1R peptide agonist DAKD both stimulate B1R-mediated nitric oxide production via eNOS and iNOS, but the signalling pathways differ between the ACE inhibitor and peptide agonist [].
The present data show that ACE inhibitor activates iNOS-mediated nitric oxide production in cytokine-treated HLMVEC via the same signalling pathway found with peptide agonist DAKD. This could reflect species differences or a change in signalling induced by cytokine treatment. We found that B1R-dependent high-output nitric oxide in cytokine-treated HLMVEC inhibited protein kinase Cɛ (PKCɛ) [] which could also have beneficial effects on the failing heart []. Taken together, our data show that iNOS activity can be regulated post-translationally and dynamically by a GPCR-activated signalling pathway. The reason this went undetected for so long could be due to two factors. First, traditional methods for measuring iNOS activity entail treating cells or animals with agents that up-regulate iNOS expression followed by collection of blood, tissue or cell culture medium after 8–48 hrs and assaying for the nitric oxide metabolites nitrite and nitrate.
Distinguishing basal versus receptor-dependent nitric oxide production would not be possible under these conditions. In contrast, our measurement of the kinetics of real-time nitric oxide output can easily differentiate these processes. Second, most work on iNOS has been conducted with rodent macrophages or macrophage cell lines where iNOS expression can be induced to very high levels, leading to a high background basal activity.
Thus, under these conditions, receptor stimulation would activate only a small fraction of the total iNOS present ( e.g. Receptor expression could be rate limiting), making it difficult to detect. Indeed, we have detected B1R-mediated activation of iNOS in the mouse macrophage-like cell line, RAW264.7, but the relative increase in overall nitric oxide production is much less than seen in HLMVEC (Brovkovych V, Skidgel, RA, unpublished).
In human cells, iNOS is induced to only relatively low levels in response to inflammatory mediators due to epigenetic silencing []. Thus, GPCR-dependent activation of iNOS provides a mechanism for generating high output nitric oxide in human cells without the need for high expression levels. B1R-dependent activation of high output nitric oxide in endothelial cells could play important roles in regulating vascular permeability. Low output nitric oxide generally promotes barrier function whereas high output nitric oxide, especially when combined with oxidants, is damaging and increases permeability. Indeed, a recent study showed that endothelial-specific expression of B1R in transgenic rats markedly enhanced their susceptibility to endotoxic shock []. Acknowledgements We thank Dr. Tiffany Sharma and Debra Salvi of the Molecular Resources Core for amplifying and preparing plasmids for use in these studies.
This work was supported by the National Institutes of Health Grants HL60678, DK 41431 and HL36473. Ancillary Article Information.
Abstract Gram-negative bacteria are associated with a wide spectrum of infectious diseases in humans. Inflammasomes are cytosolic protein complexes that are assembled when the cell encounters pathogens or other harmful agents. The non-canonical caspase-4/5 inflammasome is activated by gram-negative bacteria-derived lipopolysaccharide (LPS) and by endogenous oxidized phospholipids. Protein secretion is a critical component of the innate immune response. Here we have used label-free quantitative proteomics to characterize global protein secretion in response to non-canonical inflammasome activation upon intracellular LPS recognition in human primary macrophages. Before proteomics, the total secretome was separated into two fractions: enriched extracellular vesicle (EV) fraction and rest-secretome (RS) fraction using size-exclusion centrifugation.
We identified 1048 proteins from EV fraction and 1223 proteins from RS fraction. From these, 640 were identified from both fractions suggesting that the non-canonical inflammasome activates multiple, partly overlapping protein secretion pathways. We identified several secreted proteins that have a critical role in host response against severe gram negative bacterial infection.
The soluble secretome (RS fraction) was highly enriched with inflammation-associated proteins upon intracellular LPS recognition. Several ribosomal proteins were highly abundant in the EV fraction upon infection, and our data strongly suggests that secretion of translational machinery and concomitant inhibition of translation is an important part of host response against gram-negative bacteria sensing caspase-4/5 inflammasome. Intracellular recognition of LPS resulted in the secretion of two metalloproteinases, ADAM10 and MMP14 in enriched EV fraction. ADAM10 release was associated with the secretion of TNF, a key inflammatory cytokine and M-CSF, an important growth factor for myeloid cells probably through ADAM10-dependent membrane shedding of these cytokines. Caspase-4/5 inflammasome activation also resulted in secretion of danger associated molecules S100A8 and prothymosin-α in the enriched EV fraction. Both S100A8 and prothymosin-α are ligands for toll-like receptor 4 recognizing extracellular LPS and they may contribute to endotoxic shock during non-canonical inflammasome activation.
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