Human Peptidoglycan Recognition Protein 1 in Innate Immunity - A Review.
Keywords: Inflammation, PGLYRP1, Disease, Innate immunity, Host defense.
The innate immune system is a host defense mechanism, conserved from insects to mammalian evolutionarily, that mediates recognition and control of invading microorganisms (An et al., 2013; Hussain et al., 2017). PGRPs are a family of pattern recognition receptors (PRRs) that bind to, and in some cases hydrolyze the peptidoglycans (PGNs) of bacterial cell walls (Nylund et al., 2017). When first insect and mammalian PGRPs are cloned in 1998, it is noticed that they all contain an amidase homology domain (Brownell et al., 2016). In 2000, a family of thirteen PGRP genes in Drosophila and a year later a family of four PGRPs in humans are identified (Chen et al., 2016). They are initially named PGRP-S, PGRP-L, and PGRP-I[alpha] and PGRP-I[beta] (for 'short', 'long', or 'intermediate' transcripts, respectively) (Choe et al., 2005).
Later, the names for human PGRPs are changed by the Human Genome Organization Gene Nomenclature Committee to PGLYRP1, PGLYRP2, PGLYRP3, and PGLYRP4, respectively, and this nomenclature has been adopted for all mammalian PGRPs (Cong et al., 2009).
One mammalian PGRP, PGLYRP-2 is secreted from liver into blood (Kashyap et al., 2017), and is also induced by bacteria in epithelial cells (Kashyap et al., 2011). The three remaining mammalian PGRPs are bactericidal or bacteriostatic proteins (Kibardin et al., 2006). PGLYRP-1 is expressed primarily in the granules of polymorphonuclear leukocytes (PMNs), and PGLYRP-3 and PGLYRP-4 are expressed in the skin, eyes, mouth, intestinal tract, saliva, and protect the host against infections.
PGLYRP1 is approximately 200 amino acids, has a signal peptide and one PGRP domain (Nylund et al., 2017), and a molecular mass of about 18-20 kDa. PGLYRP1 is highly expressed in the bone marrow in PMNs and their precursors (Persson et al., 2007), and the protein is almost exclusively present in the tertiary (secretory) granules, from which it could be released by exocytosis during phagocytosis.
Function of Human Pglyrp1
PGRPs influence host-pathogen interactions not only through their antibacterial or peptidoglycan hydrolytic properties (Yang et al., 2017), but also through their pro-inflammatory and anti-inflammatory properties that are independent of their hydrolytic and antibacterial activities (Wang et al., 2016a). They maybe play a key role both in antibacterial defenses and several inflammatory diseases (Wang et al., 2016b).
Bactericidal and bacteriostatic activity
Related research results show the functions of human PGLYRP1 in the innate immunity of neutrophils are conducive to the killing of intracellular and extracellular bacteria (Yoshida et al., 1996). Although in initial studies purified human PGLYRP-1 are only bacteriostatic, the latest results nave demonstrated that human PGLYRP-1 is bactericidal and that the bactericidal activity requires Ca2+; the earlier preparations are not bactericidal because they did not contain Ca2+.
Subsequently, some studies have demonstrated that human PGLYRP-1, PGLYRP-3, PGLYRP-4, and PGLYRP-3:4 have Zn2+-dependent bactericidal activity against both Gram-positive and Gram-negative bacteria at physiologic Zn2+ concentrations found in serum, sweat, saliva, and other body fluids (Choe et al., 2005). The requirement for Zn2+ can only be partially replaced by Ca2+ for killing of Gram-positive bacteria but not for killing of Gram-negative bacteria (Kim et al., 2003). This Zn2+ dependence explains why in their previous experiments PGLYRPs purified in the presence of Ca2+ (without Zn2+) are not bactericidal for Gram-negative bacteria and were only bactericidal for some Gram-positive bacteria.
Role in diseases
Inflammatory bowel disease (IBD)
IBD is a chronic inflammatory condition of the gastrointestinal tract (Haas et al., 2017). Triggering receptor expressed on myeloid cells 1 (TREM-1) is expressed on neutrophils and most monocytes or macrophages constitutively and potently amplifies inflammation (Hakizimana et al., 2017). Recently, PGLYRP-1 is shown to be the ligand of TREM-1 (Zulfiqar et al., 2013). PGLYRP-1 is an antimicrobial peptide stored in neutrophil granules with PGN-binding activity (Stadnicki and Colman, 2003). Neutrophil degranulation releases PGLYRP-1 that, multimerized with itself or complexed with PGN, potently activates TREM-1 causing pro-inflammatory cytokine release (Cho, 2006). As PGN is a cell wall component of all bacteria, activation of TREM-1 cells by PGLYRP-1 or PGN complexes in bacteria-rich environments potently amplifies inflammation.
Here, the ability of an anti-TREM-1 antibody to dampen the release of pro-inflammatory cytokines by colon lamina propria cells (LPCs) from patients with IBD is investigated and correlated with PGLYRP-1 levels (Du et al., 2017). Moreover, PGLYRP-1+ myeloperoxidase is a potential biomarker for predicting the effect of anti-TREM-1 therapy (Subramanian et al., 2006). These studies open the possibility for a new treatment for IBD and offer insight into PGLYRP-1 (Tanaka, 2008), combined with a neutrophil marker such as MPO, as biomarkers to predict patients who would benefit from anti-TREM-1 therapy (Vermeire and Rutgeerts, 2005).
ST-elevation myocardial infarction (STEMI)
Acute myocardial infarction (AMI) is largely categorized into two categories: ST-segment-elevation myocardial infarction (STEMI) and non-ST-segment-elevation myocardial infarction (NSTEMI) (Al Shehri and Youssef, 2016). Among the most easily accessible bio-fluids is the whole blood, containing leukocytes with informative transcripts used in their first line of immune defense and sentinels for many disease processes (Alkuraishy and Al-Gareeb, 2015). Using peripheral blood in clinical applications can also provide early and accurate information before development of the disease (Andjic et al., 2015). Accordingly, it is the potential method to be informative in disease status and of the underlying diverse disease mechanisms by the blood gene expression profiling (Bilal et al., 2015).
Blood gene expression profiling reflects the status of diseases, and characteristic molecular signature provides a novel window on gene expression preceding acute coronary events (Andrechuk and Ceolim, 2015). Fortunately, the correlation results have indicated that PGLYRP1, IRAK3 and VNN3 are more specific and sensitive diagnostic biomarkers for STEMI than traditional CK-MB or troponin by a simple ELISA method. Ironically, they are the most sensitive STEMI biomarkers, none has been reported for cardiovascular disease or cardiac markers.
The thiazolidinedione medications (TZDs), pioglitazone and rosiglitazone, improve a number of inflammatory markers associated with cardiovascular disease (CVD) and have favorable effects on imaging intermediates of atherosclerosis including carotid intima-media thickness (Milasan et al., 2015), vascular inflammation, restenosis following stent implantation (Aydin et al., 2015), and de novo coronary artery disease progression. Although rosiglitazone favorably affects myriad intermediate markers of atherosclerosis (Hong et al., 2015), it appears to increase myocardial infarction (MI) risk.
Some studies have found that rosiglitazone has a unfavorable effects on three novel inflammatory biomarkers previously shown to independently associate with atherosclerosis (LT[beta]R, PGLYRP-1, and CCL23) and a favorable effect on another novel biomarker (Ling et al., 2015), sRAGE, which previously studies have been shown to be inversely associated with atherosclerosis (Lubrano et al., 2015).
PGN is detectable in varying levels in the circulation and has been identified by immunohistochemical staining in human atherosclerotic specimens. PGN may promote localized inflammation in non-mucosal sites by stimulating the production of PGRPs. Among four known human sub-types of PGRP, PGLYRP-1 is expressed primarily in PMN granules, likely functioning as an antibacterial protein. Plasma levels of PGLYRP-1 may represent the systemic response to bacterial exposure, possibly underpinning the observed associations between bacterial infection and exposure with coronary heart disease.
Rheumatoid arthritis (RA)
RA is a chronic inflammatory and autoimmune disease characterized by inflammation of the synovial membrane leading to the destruction of affected joints (Takamatsu et al., 2016). The study of polymorphisms of genes differentially expressed may lead to the identification of putative causal genetic variants in multifactorial diseases such as RA (Adtani and Malathi, 2015). The list of genes to explore is established on the basis of the differential expression in RA vs controls, and included four up-regulated genes (S100A8, PGLYRP1, RNASE2, and LY96) and two down-regulated genes (RUNX3 and IL2RB) (Ataee et al., 2015). The hypothesis is that the differentially expressed genes are associated with RA, using family-based methodology (Bougea et al., 2015).
Recent studies have shown that PGRPs influence host-pathogen interactions through their pro-inflammatory or anti-inflammatory properties, which are independent of their antibacterial activities, modulating the balance between inflammatory T-helper (Th)17 cells and regulatory T cells. Taking into consideration the potential role of bacteria in the pathogenesis of RA, an up-regulation of PGLYRP1 in the context of the HLA-DRB1 shared epitope (SE) may influence the onset of the disease affecting inflammatory circuits, cytokine production, and possibly antigen presentation (Boughrara et al., 2015).
Skin melanoma and renal carcinoma
During the last decade novel approaches for cancer treatment have been developed. Anti-tumor vaccination is considered to be one of the most promising of these (Goncalves et al., 2015). One of the possible ways to induce specific immune response is the use of tumor rejection antigens discovered during recent years (Goncalves et al., 2015). Clinically important results of vaccinotherapy are achieved in patients with melanoma and renal carcinoma in a number of studies (Kao et al., 1992). The results with this treatment are comparable to chemotherapy and immunotherapy.
Recently, a novel gene, tag7 is identified, also known as PGRP-S. A phase I/II trial has been undertaken to define the feasibility, safety and anti-tumor effects of the autologous vaccine prepared by transferring tag7/PGRP-S gene into malignant melanoma and renal cell carcinoma cells. Related findings have indicated that vaccinotherapy of patients with skin melanoma and renal carcinoma with the tag7-modified autologous tumor cells is safe and do not have any significant side-effects. The use of genetically modified autologous tumor cells will be a promising approach for cancer therapy in the future.
Human PGLYRP1 plays a role in innate immunity in the context of neutrophils by contributing to the killing of intracellular and extracellular bacteria. PGLYRP-1 have Zn2+-dependent bactericidal activity against both Gram-positive and Gram-negative bacteria. Besides, the requirement for Zn2+ can only be partially replaced by Ca2+ for killing of Gram-positive bacteria but not for killing of Gram-negative bacteria and also influence host-pathogen interactions through their pro-inflammatory and anti-inflammatory properties.
Moreover, the PGLYRP1 dimer in human serum and polymorphonuclear cells is detected, from where it is secreted after degranulation; these cells being a possible source of serum PGLYRP1; these cells being a possible source of serum PGLYRP1. In addition, all PGRP protect cells from PGN-nduced apoptosis. PGRP increase THP-1 cell proliferation and enhance activation by PGN. PGLYRP1-PGN complexes increase the membrane expression of CD14, CD80 and CD86, and enhance secretion of interleukin-8, interleukin-12 and tumor necrosis factor-[alpha], but reduce interleukin-10, clearly inducing an inflammatory profile.
Recent findings indicate that the adaptive arm of immunity is governed by the innate immunity mechanisms that control co-stimulatory signaling of antigen-presenting cells (APCs) (Fang et al., 2015). The combination of cytokines effecting both innate and acquired immune response taken together with tumor antigens may significantly improve overall efficiency of anti-tumor vaccination.
Although many functions of human PGLYRP1 have been identified, it is still possible that human PGLYRP1 have other unidentified functions, because many mammalian proteins have evolved to have multiple functions. In addition, it is still not clear how PGLYRP1 affects the cytokines in human various diseases.
Statement of conflict of interest
The authors in the paper showed no potential conflicts of interest.
Adtani, P. and Malathi, N., 2015. Epstein-Barr virus and its association with rheumatoid arthritis and oral lichen planus. J. Oral Maxillofac. Pathol., 19: 282-285. https://doi.org/10.4103/0973-029X.174643
Al Shehri, M.A. and Youssef, A.A., 2016. Acute myocardial infarction with multiple coronary thromboses in a young addict of amphetamines and benzodiazepines. J. Saudi Heart Assoc., 28: 180-184. https://doi.org/10.1016/j.jsha.2015.11.004
Al Kuraishy, H.M. and Al-Gareeb, A.I., 2015. New insights into the role of metformin effects on serum omentin-1 levels in acute myocardial infarction: Cross-sectional study. Emerg. Med. Int., 2015: 283021.
An, J.H., Kurokawa, K., Jung, D.J., Kim, M.J., Kim, C.H., Fujimoto, Y., Fukase, K., Coggeshall, K.M. and Lee, B.L., 2013. Human SAP is a novel peptidoglycan recognition protein that induces complement-independent phagocytosis of Staphylococcus aureus. J. Immunol., 191: 3319-3327. https://doi.org/10.4049/jimmunol.1300940
Andjic, M., Spiroski, D., Ilic Stojanovic, O., Vidakovic, T., Lazovic, M., Babic, D., Ristic, A., Mazic, S., Zdravkovic, M. and Otasevic, P., 2015. Effects of short-term exercise training in patients following acute myocardial infarction treated with primary percutaneous coronary intervention. Eur. J. Phys. Rehabil. Med., 52: 364-369.
Andrechuk, C.R. and Ceolim, M.F., 2015. High risk for obstructive sleep apnea in patients with acute myocardial infarction. Rev. Lat. Am. Enfermagem., 23: 797-805. https://doi.org/10.1590/0104-1169.0511.2617
Ataee, R.A., Kashefi, R., Alishiri, G.H. and Esmaieli, D., 2015. Assay of blood and synovial fluid of patients with rheumatoid arthritis for Staphylococcus aureus enterotoxin D: Absence of bacteria but presence of its toxin. Jundishapur J. Microbiol., 8: e28395. https://doi.org/10.5812/jjm.28395
Aydin, K., Canpolat, U., Akin, S., Dural, M., Karakaya, J., Aytemir, K., Ozer, N. and Gurlek, A., 2015. Chemerin is not associated with subclinical atherosclerosis markers in prediabetes and diabetes. Anatolian J. Cardiol., https://doi.org/10.5152/AnatolJCardiol.2015.6629
Bilal, M., Haseeb, A. and Sher Khan, M.A., 2015. Intracoronary infusion of Wharton's jelly-derived mesenchymal stem cells: A novel treatment in patients of acute myocardial infarction. J. Pak. med. Assoc., 65: 1369.
Bougea, A., Anagnostou, E., Konstantinos, G., George, P., Triantafyllou, N. and Kararizou, E., 2015. A systematic review of peripheral and central nervous system involvement of rheumatoid arthritis, systemic lupus erythematosus, primary sjogren's syndrome, and associated immunological profiles. Int. J. Chronic Dis., 2015: 910352. https://doi.org/10.1155/2015/910352
Boughrara, W., Aberkane, M., Fodil, M., Benzaoui, A., Dorgham, S., Zemani, F., Dahmani, C., Petit Teixeira, E. and Boudjema, A., 2015. Impact of MTHFR rs1801133, MTHFR rs1801131 and ABCB1 rs1045642 polymorphisms with increased susceptibility of rheumatoid arthritis in the West Algerian population: A case-control study. Acta Reumatol. Port., 40: 363-371.
Brownell, N.K., Khera, A., de Lemos, J.A., Ayers, C.R. and Rohatgi, A., 2016. Association between peptidoglycan recognition protein-1 and incident atherosclerotic cardiovascular disease events: The Dallas heart study. J. Am. Coll. Cardiol., 67: 2310-2312. https://doi.org/10.1016/S0735-1097(16)31840-X
Chen, K., Zhou, L., Chen, F., Peng, Y. and Lu, Z., 2016. Peptidoglycan recognition protein-S5 functions as a negative regulator of the antimicrobial peptide pathway in the silkworm, Bombyx mori. Develop. Comp. Immunol., 61: 126-135. https://doi.org/10.1016/j.dci.2016.03.023
Cho, J., 2006. Genetic advances in inflammatory bowel disease. Curr. Treat. Options Gastroenterol., 9: 191-200. https://doi.org/10.1007/s11938-006-0038-z
Choe, K.M., Lee, H. and Anderson, K.V., 2005. Drosophila peptidoglycan recognition protein LC (PGRP-LC) acts as a signal-transducing innate immune receptor. Proc. natl. Acad. Sci. U.S.A., 102: 1122-1126. https://doi.org/10.1073/pnas.0404952102
Cong, M., Song, L., Qiu, L., Li, C., Wang, B., Zhang, H. and Zhang, L., 2009. The expression of peptidoglycan recognition protein-S1 gene in the scallop Chlamys farreri was enhanced after a second challenge by Listonella anguillarum. J. Inverteb. Pathol., 100: 120-122. https://doi.org/10.1016/j.jip.2008.10.004
Du, L., Kim, J.J., Shen, J., Chen, B. and Dai, N., 2017. KRAS and TP53 mutations in inflammatory bowel disease-associated colorectal cancer: A meta-analysis. Oncotarget, 8: 22175-22186. https://doi.org/10.18632/oncotarget.14549
Fang, R.H., Kroll, A.V. and Zhang, L., 2015. Nanoparticle-based manipulation of antigen-presenting cells for cancer immunotherapy. Small, 11: 5483-5496. https://doi.org/10.1002/smll.201570249
Goncalves, C.P., Trope, B.M. and Ramos, E.S.M., 2015. Non-melanoma skin cancer in renal transplant recipients: A study in a Brazilian reference center. Clin. Cosmet. Invest. Dermatol., 8: 339-344.
Haas, L., Chevalier, R., Major, B.T., Enders, F., Kumar, S. and Tung, J., 2017. Biologic agents are associated with excessive weight gain in children with inflammatory bowel disease. Dig. Dis. Sci., 62: 3110-3116. https://doi.org/10.1007/s10620-017-4745-1
Hakizimana, A., Ahmed, I., Russell, R., Wright, M. and Afzal, N.A., 2017. Challenges of modern day transition care in inflammatory bowel disease: From inflammatory bowel disease to biosimilars. World J. Gastroenterol., 23: 4473-4479. https://doi.org/10.3748/wjg.v23.i25.4473
Hong, J., Maron, D.J., Shirai, T., Weyand, C.M., 2015. Accelerated atherosclerosis in patients with chronic inflammatory rheumatologic conditions. Int. J. clin. Rheumtol., 10: 365-381. https://doi.org/10.2217/ijr.15.33
Hussain, Z., Khan IR., Malik TH. and Shan SIA., 2017. Screening of USDA cotton accessions against sucking insect pests complex and cotton leaf curl virus (CLCuV) disease with major emphasis on abiotic factors. Pakistan J. Zool., 49: 1159-1173.
Kao, G.F., Helwig, E.B. and Graham, J.H., 1992. Balloon cell malignant melanoma of the skin. A clinicopathologic study of 34 cases with histochemical, immunohistochemical, and ultrastructural observations. Cancer, 69: 2942-2952. https://doi.org/10.1002/1097-0142(19920615)69:123.0.CO;2-0
Kashyap, D.R., Wang, M., Liu, L.H., Boons, G.J., Gupta, D. and Dziarski, R., 2011. Peptidoglycan recognition proteins kill bacteria by activating protein-sensing two-component systems. Nat. Med., 17: 676-683. https://doi.org/10.1038/nm.2357
Kashyap, D.R., Kuzma, M., Kowalczyk, D.A., Gupta, D. and Dziarski, R., 2017. Bactericidal peptidoglycan recognition protein induces oxidative stress in Escherichia coli through a block in respiratory chain and increase in central carbon catabolism. Mol. Microbiol., 105: 755-776. https://doi.org/10.1111/mmi.13733
Kibardin, A., Karpova, T., Sapenko, T., Vazquez-Boland, J.A., Kiselev, S. and Ermolaeva, S., 2006. Mammalian peptidoglycan recognition protein TagL inhibits Listeria monocytogenes invasion into epithelial cells. FEMS Immunol. med. Microbiol., 46: 284-290. https://doi.org/10.1111/j.1574-695X.2005.00038.x
Kim, M.S., Byun, M. and Oh, B.H., 2003. Crystal structure of peptidoglycan recognition protein LB from Drosophila melanogaster. Nat. Immunol., 4: 787-793. https://doi.org/10.1038/ni952
Ling, Y., Jiang, J., Gui, M., Liu, L., Aleteng, Q., Wu, B., Wang, S., Liu, X. and Gao, X., 2015. Thyroid function, prevalent coronary heart disease, and severity of coronary atherosclerosis in patients undergoing coronary angiography. Int. J. Endocrinol., 2015: 708272. https://doi.org/10.1155/2015/708272
Lubrano, V., Venturi, E., Balzan, S., Baldi, S. and Natali, A., 2015. Impact of risk factor for atherosclerosis on microvascular endothelial function: An in vitro study. Theor. Biol. Forum, 108: 75-88.
Milasan, A., Ledoux, J. and Martel, C., 2015. Lymphatic network in atherosclerosis: the underestimated path. Future Sci. OA, 1: FSO61. https://doi.org/10.4155/fso.15.61
Nylund, K.M., Ruokonen, H., Sorsa, T., Heikkinen, A.M., Meurman, J.H., Ortiz, F., Tervahartiala, T., Furuholm, J. and Bostanci, N., 2017. Association of the salivary triggering receptor expressed on myeloid cells/ its ligand peptidoglycan recognition protein 1 axis with oral inflammation in kidney disease. J. Periodontol., 28: 1-17. https://doi.org/10.1902/jop.2017.170218
Persson, C., Oldenvi, S. and Steiner, H., 2007. Peptidoglycan recognition protein LF: A negative regulator of Drosophila immunity. Insect Biochem. Mol. Biol., 37: 1309-1316. https://doi.org/10.1016/j.ibmb.2007.08.003
Stadnicki, A. and Colman, R.W., 2003. Experimental models of inflammatory bowel disease. Arch. Immunol. Ther. Exp., 51: 149-155.
Subramanian, S., Campbell, B.J. and Rhodes, J.M., 2006. Bacteria in the pathogenesis of inflammatory bowel disease. Curr. Opin. Infect. Dis., 19: 475-484. https://doi.org/10.1097/01.qco.0000244054.69253.f3
Takamatsu, N., Takizawa, H., Sugawara, H. and Ogawa, Y., 2016. Acute interstitial nephritis with membranous nephropathy in bucillamine-treated rheumatoid arthritis. CEN Case Rep., 5: 103-107. https://doi.org/10.1007/s13730-015-0204-z
Tanaka, K., 2008. Expression of Toll-like receptors in the intestinal mucosa of patients with inflammatory bowel disease. Expert Rev. Gastroenterol. Hepatol., 2: 193-196. https://doi.org/10.1586/1747422.214.171.124
Vermeire, S. and Rutgeerts, P., 2005. Current status of genetics research in inflammatory bowel disease. Genes Immunity, 6: 637-645. https://doi.org/10.1038/sj.gene.6364257
Wang, N., Hirata, A., Nokihara, K., Fukase, K. and Fujimoto, Y., 2016a. Peptidoglycan microarray as a novel tool to explore protein-ligand recognition. Biopolymers, 106: 422-429. https://doi.org/10.1002/bip.22807
Wang, Z.Z., Shi, M., Huang, Y.C., Wang, X.W., Stanley, D. and Chen, X.X., 2016b. A peptidoglycan recognition protein acts in whitefly (Bemisia tabaci) immunity and involves in Begomovirus acquisition. Scient. Rep., 6: 37806. https://doi.org/10.1038/srep37806
Yang, P.J., Zhan, M.Y., Ye, C., Yu, X.Q. and Rao, X.J., 2017. Molecular cloning and characterization of a short peptidoglycan recognition protein from silkworm Bombyx mori. Insect Mol. Biol., 26: 665-667. https://doi.org/10.1111/imb.12330
Yoshida, H., Kinoshita, K. and Ashida, M., 1996. Purification of a peptidoglycan recognition protein from hemolymph of the silkworm, Bombyx mori. J. Biol. Chem., 271: 13854-13860. https://doi.org/10.1074/jbc.271.23.13854
Zulfiqar, F., Hozo, I., Rangarajan, S., Mariuzza, R.A., Dziarski, R. and Gupta, D., 2013. Genetic association of peptidoglycan recognition protein variants with inflammatory bowel disease. PLoS One, 8: e67393. https://doi.org/10.1371/journal.pone.0067393
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|Publication:||Pakistan Journal of Zoology|
|Date:||Jun 30, 2019|
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