Modified polymeric biomaterials with antimicrobial and immunomodulating properties.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 Apr 2024
Historique:
received: 01 12 2023
accepted: 02 04 2024
medline: 6 4 2024
pubmed: 6 4 2024
entrez: 5 4 2024
Statut: epublish

Résumé

The modification of the surgical polypropylene mesh and the polytetrafluoroethylene vascular prosthesis with cecropin A (small peptide) and puromycin (aminonucleoside) yielded very stable preparations of modified biomaterials. The main emphasis was placed on analyses of their antimicrobial activity and potential immunomodulatory and non-cytotoxic properties towards the CCD841 CoTr model cell line. Cecropin A did not significantly affect the viability or proliferation of the CCD 841 CoTr cells, regardless of its soluble or immobilized form. In contrast, puromycin did not induce a significant decrease in the cell viability or proliferation in the immobilized form but significantly decreased cell viability and proliferation when administered in the soluble form. The covalent immobilization of these two molecules on the surface of biomaterials resulted in stable preparations that were able to inhibit the multiplication of Staphylococcus aureus and S. epidermidis strains. It was also found that the preparations induced the production of cytokines involved in antibacterial protection mechanisms and stimulated the immune response. The key regulator of this activity may be related to TLR4, a receptor recognizing bacterial LPS. In the present study, these factors were produced not only in the conditions of LPS stimulation but also in the absence of LPS, which indicates that cecropin A- and puromycin-modified biomaterials may upregulate pathways leading to humoral antibacterial immune response.

Identifiants

pubmed: 38580807
doi: 10.1038/s41598-024-58730-3
pii: 10.1038/s41598-024-58730-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8025

Subventions

Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084
Organisme : National Science Centre in Poland
ID : Opus 2017/25/B/NZ7/01084

Informations de copyright

© 2024. The Author(s).

Références

Andrade-Del Olmo, J., Ruiz-Rubio, L., Perez-Alvarez, L., Saez-Martinez, V. & Vilas-Vilela, J. L. Antibacterial coatings for improving the performance of biomaterials. Coatings https://doi.org/10.3390/coatings10020139 (2020).
doi: 10.3390/coatings10020139
Narayana, P. S. V. V. S. & Srihari, P. S. V. V. A review on surface modifications and coatings on implants to prevent biofilm. Regen Eng. Transl. Med. 6(3), 330–346. https://doi.org/10.1007/s40883-019-00116-3 (2020).
doi: 10.1007/s40883-019-00116-3
Wang, G. et al. Antibacterial peptides-loaded bioactive materials for the treatment of bone infection. Colloids Surf. B Biointerfaces 225, 113255. https://doi.org/10.1016/j.colsurfb.2023.113255 (2023).
doi: 10.1016/j.colsurfb.2023.113255 pubmed: 36924650
Guillaume, O. et al. Fabrication of silk mesh with enhanced cytocompatibility: Preliminary in vitro investigation toward cell-based therapy for hernia repair. J. Mater. Sci. Mater. Med. 27(2), 37. https://doi.org/10.1007/s10856-015-5648-3 (2016).
doi: 10.1007/s10856-015-5648-3 pubmed: 26704554
Ebara, M. Apoptotic cell-mimetic polymers for anti-inflammatory therapy. Chonnam. Med. J. 55(1), 1–7. https://doi.org/10.4068/cmj.2019.55.1.1 (2019).
doi: 10.4068/cmj.2019.55.1.1 pubmed: 30740334 pmcid: 6351328
Woitschach, F. et al. In vitro study of the interaction of innate immune cells with liquid silicone rubber coated with zwitterionic methyl methacrylate and thermoplastic polyurethanes. Materials (Basel) https://doi.org/10.3390/ma14205972 (2021).
doi: 10.3390/ma14205972 pubmed: 34683562
Whitaker, R., Hernaez-Estrada, B., Hernandez, R. M., Santos-Vizcaino, E. & Spiller, K. L. Immunomodulatory biomaterials for tissue repair. Chem. Rev. 121(18), 11305–11335. https://doi.org/10.1021/acs.chemrev.0c00895 (2021).
doi: 10.1021/acs.chemrev.0c00895 pubmed: 34415742
Dias, G. J. et al. The adaptive immune response to porous regenerated keratin as a bone graft substitute in an ovine model. Int. J. Biol. Macromol. 165, 100–106. https://doi.org/10.1016/j.ijbiomac.2020.09.133 (2020).
doi: 10.1016/j.ijbiomac.2020.09.133 pubmed: 32980411
Kohler, R. et al. Association of systemic antibody response against polyethylene terephthalate with inflammatory serum cytokine profile following implantation of differently coated vascular prostheses in a rat animal model. J. Biomed. Mater. Res. A 110(1), 52–63. https://doi.org/10.1002/jbm.a.37265 (2022).
doi: 10.1002/jbm.a.37265 pubmed: 34245083
Sun, J. et al. Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation. Bioact. Mater. 9, 1–14. https://doi.org/10.1016/j.bioactmat.2021.10.003 (2022).
doi: 10.1016/j.bioactmat.2021.10.003 pubmed: 34820551
Tang, R. et al. Risk factors for surgical site infection after elective resection of the colon and rectum: A single-center prospective study of 2,809 consecutive patients. Ann. Surg. 234(2), 181–189. https://doi.org/10.1097/00000658-200108000-00007 (2001).
doi: 10.1097/00000658-200108000-00007 pubmed: 11505063 pmcid: 1422004
Mulita, F. et al. Postoperative sepsis after colorectal surgery: A prospective single-center observational study and review of the literature. Gastroenter. Rev. 17(1), 47–51. https://doi.org/10.5114/pg.2021.106083 (2022).
doi: 10.5114/pg.2021.106083
Kasparek, M. et al. Quality of life after coloanal anastomosis and abdominoperineal resection for distal rectal cancers: Sphincter preservation vs quality of life. Color. Dis. 13(8), 872–877. https://doi.org/10.1111/j.1463-1318.2010.02347.x (2011).
doi: 10.1111/j.1463-1318.2010.02347.x
Duclos, J. et al. Immediate outcome, long-term function and quality of life after extended colectomy with ileorectal or ileosigmoid anastomosis. Color. Dis. 16(8), O288–O296. https://doi.org/10.1111/codi.12558 (2014).
doi: 10.1111/codi.12558
Bitar, K. N. & Raghavan, S. Intestinal tissue engineering: Current concepts and future vision of regenerative medicine in the gut. Neurogastroenterol. Motil. 24(1), 7–19. https://doi.org/10.1111/j.1365-2982.2011.01843.x (2012).
doi: 10.1111/j.1365-2982.2011.01843.x pubmed: 22188325 pmcid: 3248673
O’Neill, J. D., Pinezich, M. R., Guenthart, B. A. & Vunjak-Novakovic, G. Gut bioengineering strategies for regenerative medicine. Am. J. Physiol. Gastrointest Liver Physiol. 320(1), G1–G11. https://doi.org/10.1152/ajpgi.00206.2020 (2021).
doi: 10.1152/ajpgi.00206.2020 pubmed: 33174453
Anderson, J. Biocompatibility. Polym. Sci. A Compreh. Ref. 9, 363–383. https://doi.org/10.1016/B978-0-444-53349-4.00229-6 (2012).
doi: 10.1016/B978-0-444-53349-4.00229-6
Cohn, M., Unnanuntana, A., Pannu, T., Warner, S. & Lane, J. Materials in fracture fixation. Reference module in materials science and materials engineering. Comprehensive Biomaterials II. 7 ed., 2017. p. 278-97
Suffo, M. & Revenga, C. Biomechanical analysis of non-metallic biomaterial in the manufacture of a new knee prosthesis. Materials (Basel) https://doi.org/10.3390/ma14205951 (2021).
doi: 10.3390/ma14205951 pubmed: 34683542
Bhattacharjee, B., Ghosh, S., Patra, D. & Haldar, J. Advancements in release-active antimicrobial biomaterials: A journey from release to relief. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 14(1), e1745. https://doi.org/10.1002/wnan.1745 (2022).
doi: 10.1002/wnan.1745 pubmed: 34374498
Li, G. Y., Lai, Z. H. & Shan, A. S. Advances of antimicrobial peptide-based biomaterials for the treatment of bacterial infections. Adv. Sci. https://doi.org/10.1002/advs.202206602 (2023).
doi: 10.1002/advs.202206602
Guillaume, O. et al. Infections associated with mesh repairs of abdominal wall hernias: Are antimicrobial biomaterials the longed-for solution?. Biomaterials 167, 15–31. https://doi.org/10.1016/j.biomaterials.2018.03.017 (2018).
doi: 10.1016/j.biomaterials.2018.03.017 pubmed: 29554478
Pandey, A. T. et al. Emerging paradigm against global antimicrobial resistance via bioprospecting of mushroom into novel nanotherapeutics development. Trends Food Sci. Tech. 106, 333–344. https://doi.org/10.1016/j.tifs.2020.10.025 (2020).
doi: 10.1016/j.tifs.2020.10.025
Kamboj, M. et al. Risk of surgical site infection (SSI) following colorectal resection is higher in patients with disseminated cancer: An NCCN member cohort study. Infect. Cont. Hosp. Ep. 39(5), 555–562. https://doi.org/10.1017/ice.2018.40 (2018).
doi: 10.1017/ice.2018.40
Serra-Aracil, X. et al. Surgical site infection in elective operations for colorectal cancer after the application of preventive measures. Arch. Surg. 146(5), 606–612. https://doi.org/10.1001/archsurg.2011.90 (2011).
doi: 10.1001/archsurg.2011.90 pubmed: 21576613
Skerlavaj, B. & Boix-Lemonche, G. The potential of surface-immobilized antimicrobial peptides for the enhancement of orthopaedic medical devices: A review. Antibiotics (Basel) https://doi.org/10.3390/antibiotics12020211 (2023).
doi: 10.3390/antibiotics12020211 pubmed: 36830122
Silva, R. R. et al. Chemical immobilization of antimicrobial peptides on biomaterial surfaces. Front. Biosci. (Schol. Ed) 8(1), 129–142. https://doi.org/10.2741/s453 (2016).
doi: 10.2741/s453 pubmed: 26709903
Tarawneh, O. et al. Determination of antimicrobial and antibiofilm activity of combined LVX and AMP impregnated in p(HEMA) hydrogel. Appl. Sci. Basel https://doi.org/10.3390/app11188345 (2021).
doi: 10.3390/app11188345
Tan, A., Xu, F. S., Yokoyama, C., Yano, S. & Konno, H. Design, synthesis, and evaluation of the self-assembled antimicrobial peptides based on the ovalbumin-derived peptide TK913. J. Pept. Sci. https://doi.org/10.1002/psc.3375 (2022).
doi: 10.1002/psc.3375 pubmed: 34725889
Shao, H. et al. Bio-inspired peptide-conjugated liposomes for enhanced planktonic bacteria killing and biofilm eradication. Biomaterials 300, 122183. https://doi.org/10.1016/j.biomaterials.2023.122183 (2023).
doi: 10.1016/j.biomaterials.2023.122183 pubmed: 37302278
Xiang, J. Y. et al. Mesh-like electrospun membrane loaded with atorvastatin facilitates cutaneous wound healing by promoting the paracrine function of mesenchymal stem cells. Stem. Cell Res. Ther. https://doi.org/10.1186/s13287-022-02865-5 (2022).
doi: 10.1186/s13287-022-02865-5 pubmed: 36414991 pmcid: 9682817
Liu, P. B., Fu, K., Zeng, X. M., Chen, N. L. & Wen, X. J. Fabrication and characterization of composite meshes loaded with antimicrobial peptides. Acs. Appl. Mater. Inter. 11(27), 24609–24617. https://doi.org/10.1021/acsami.9b07246 (2019).
doi: 10.1021/acsami.9b07246
Campoccia, D. et al. Antibacterial activity on orthopedic clinical isolates and cytotoxicity of the antimicrobial peptide dadapin-1. Int. J. Mol. Sci. https://doi.org/10.3390/ijms24010779 (2023).
doi: 10.3390/ijms24010779 pubmed: 38069365 pmcid: 10707472
Ajish, C. et al. A novel hybrid peptide composed of Lfcinb6 and KR-12-a4 with enhanced antimicrobial, anti-inflammatory and anti-biofilm activities. Sci. Rep. 12(1), 4365. https://doi.org/10.1038/s41598-022-08247-4 (2022).
doi: 10.1038/s41598-022-08247-4 pubmed: 35288606 pmcid: 8921290
Wang, L. et al. Potent antibacterial and antibiofilm activities of Ticbf-14, a peptide with increased stability against trypsin. J. Microbiol. 60(1), 89–99. https://doi.org/10.1007/s12275-022-1368-9 (2022).
doi: 10.1007/s12275-022-1368-9 pubmed: 34964945
Peng, C. et al. Mechanisms of action of the antimicrobial peptide cecropin in the killing of Candida albicans. Life (Basel) https://doi.org/10.3390/life12101581 (2022).
doi: 10.3390/life12101581 pubmed: 36362904 pmcid: 9788439
Xue, Q. et al. Anti-infective biomaterials with surface-decorated tachyplesin I. Biomaterials 178, 351–362. https://doi.org/10.1016/j.biomaterials.2018.05.008 (2018).
doi: 10.1016/j.biomaterials.2018.05.008 pubmed: 29778319
Griesser, S. S., Jasieniak, M., Vasilev, K. & Griesser, H. J. Antimicrobial peptides grafted onto a plasma polymer interlayer platform: Performance upon extended bacterial challenge. Coatings 11(1), 68. https://doi.org/10.3390/coatings11010068 (2021).
doi: 10.3390/coatings11010068
Atefyekta, S. et al. Antimicrobial peptide-functionalized mesoporous hydrogels. ACS Biomater. Sci. Eng. 7(4), 1693–1702. https://doi.org/10.1021/acsbiomaterials.1c00029 (2021).
doi: 10.1021/acsbiomaterials.1c00029 pubmed: 33719406 pmcid: 8153390
Brown, C. N. & Finch, J. G. Which mesh for hernia repair?. Ann. Roy Coll. Surg. 92(4), 272–278. https://doi.org/10.1308/003588410x12664192076296 (2010).
doi: 10.1308/003588410x12664192076296
Rovner, E., de Tayrac, R., Kirschner-Hermanns, R., Veit-Rubin, N. & Anding, R. Is polypropylene mesh material fundamentally safe for use as a reconstructive material in vaginal surgery: Ici-rs 2019?. Neurourol. Urodynam. 39, S132–S139. https://doi.org/10.1002/nau.24312 (2020).
doi: 10.1002/nau.24312
Anghel, R., Jitaru, D., Badescu, L., Ciocoiu, M. & Badescu, M. The cytotoxic effect of cecropin A and cecropin B on the MDA-MB-231 and M14K tumour cell lines. J. Biomed. Sci. Eng. 7, 504–515. https://doi.org/10.4236/jbise.2014.78052 (2014).
doi: 10.4236/jbise.2014.78052
Sang, M., Zhang, J. & Zhuge, Q. Selective cytotoxicity of the antibacterial peptide ABP-dHC-cecropin A and its analog towards leukemia cells. Eur. J. Pharmacol. 803, 138–147. https://doi.org/10.1016/j.ejphar.2017.03.054 (2017).
doi: 10.1016/j.ejphar.2017.03.054 pubmed: 28347740
Lee, E. et al. Structure-activity relationships of cecropin-like peptides and their interactions with phospholipid membrane. Bmb. Rep. 46(5), 282–287. https://doi.org/10.5483/BMBRep.2013.46.5.252 (2013).
doi: 10.5483/BMBRep.2013.46.5.252 pubmed: 23710640 pmcid: 4133896
Nguyen, L., Wruck, W., Erichsen, L., Graffmann, N. & Adjaye, J. The nephrotoxin puromycin aminonucleoside induces injury in kidney organoids differentiated from induced pluripotent stem cells. Cells https://doi.org/10.3390/cells11040635 (2022).
doi: 10.3390/cells11040635 pubmed: 36497038 pmcid: 9737670
Aviner, R. The science of puromycin: From studies of ribosome function to applications in biotechnology. Comput. Struct. Biotechnol. J. 18, 1074–1083. https://doi.org/10.1016/j.csbj.2020.04.014 (2020).
doi: 10.1016/j.csbj.2020.04.014 pubmed: 32435426 pmcid: 7229235
Jung, J. H. et al. P53-dependent apoptotic effect of puromycin via binding of ribosomal protein L5 and L11 to MDM2 and its combination effect with RITA or doxorubicin. Cancers (Basel) https://doi.org/10.3390/cancers11040582 (2019).
doi: 10.3390/cancers11040582 pubmed: 31888257 pmcid: 6896094
Chan, C. et al. Incompatibility of chemical protein synthesis inhibitors with accurate measurement of extended protein degradation rates. Pharmacol. Res. Perspect. https://doi.org/10.1002/prp2.359 (2017).
doi: 10.1002/prp2.359 pubmed: 28971619 pmcid: 5625163
Kapusetti, G., More, N. & Choppadandi, M. Introduction to ideal characteristics and advanced biomedical applications of biomaterials. Biomed. Eng. Appl. Healthc. https://doi.org/10.1007/978-981-13-3705-5_8 (2019).
doi: 10.1007/978-981-13-3705-5_8
Moreau, A., Varey, E., Anegon, I. & Cuturi, M.-C. Effector mechanisms of rejection. Cold Spring Harbor Persp. Med. https://doi.org/10.1101/cshperspect.a015461 (2013).
doi: 10.1101/cshperspect.a015461
Yanez, M., Blanchette, J. & Jabbarzadeh, E. Modulation of inflammatory response to implanted biomaterials using natural compounds. Curr. Pharm. Des. 23(41), 6347–6357. https://doi.org/10.2174/1381612823666170510124348 (2017).
doi: 10.2174/1381612823666170510124348 pubmed: 28521709 pmcid: 5681444
Ambrożewicz, E., Tokajuk, G., Muszyńska, M., Zaręba, I. & Skrzydlewska, E. Cross talk between redox signalling and metabolic activity of osteoblasts and fibroblasts in the presence of hydroxyapatite-based biomaterials influences bone regeneration. J. Appl. Biomed. https://doi.org/10.1016/j.smim.2007.11.004 (2019).
doi: 10.1016/j.smim.2007.11.004 pubmed: 34907734
Malisan, F. et al. Interleukin-10 induces immunoglobulin G isotype switch recombination in human CD40-activated naive B lymphocytes. J. Exp. Med. 183(3), 937–947. https://doi.org/10.1084/jem.183.3.937 (1996).
doi: 10.1084/jem.183.3.937 pubmed: 8642297
McClure, R. & Massari, P. TLR-dependent human mucosal epithelial cell responses to microbial pathogens. Front. Immunol. 5, 386. https://doi.org/10.3389/fimmu.2014.00386 (2014).
doi: 10.3389/fimmu.2014.00386 pubmed: 25161655 pmcid: 4129373
Punnonen, J. et al. Interleukin 13 induces interleukin 4-independent IgG4 and IgE synthesis and CD23 expression by human B cells. Proc. Natl. Acad. Sci. USA 90(8), 3730–3734. https://doi.org/10.1073/pnas.90.8.3730 (1993).
doi: 10.1073/pnas.90.8.3730 pubmed: 8097323 pmcid: 46375
Spiegelberg, H. L. The role of interleukin-4 in IgE and IgG subclass formation. Springer Semin. Immunopathol. 12(4), 365–383. https://doi.org/10.1007/BF00225324 (1990).
doi: 10.1007/BF00225324 pubmed: 2096469
Verkaik, N. J. et al. Heterogeneity of the humoral immune response following Staphylococcus aureus bacteremia. Eur. J. Clin. Microbiol. Infect. Dis. 29(5), 509–518. https://doi.org/10.1007/s10096-010-0888-0 (2010).
doi: 10.1007/s10096-010-0888-0 pubmed: 20186449 pmcid: 2854366
Wang, J. et al. A novel cecropin B-derived peptide with antibacterial and potential anti-inflammatory properties. PeerJ 6, e5369. https://doi.org/10.7717/peerj.5369 (2018).
doi: 10.7717/peerj.5369 pubmed: 30065898 pmcid: 6064198
Xu, D. W. et al. Surface functionalization of titanium substrates with cecropin B to improve their cytocompatibility and reduce inflammation responses. Coll. Surf. B 110, 225–235. https://doi.org/10.1016/j.colsurfb.2013.04.050 (2013).
doi: 10.1016/j.colsurfb.2013.04.050
Di Vita, G. et al. Impact of different texture of polypropylene mesh on the inflammatory response. Int. J. Immunopathol. Pharmacol. 21(1), 207–214. https://doi.org/10.1177/039463200802100123 (2008).
doi: 10.1177/039463200802100123 pubmed: 18336747
Kolaczkowska, E. & Kubes, P. Neutrophil recruitment and function in health and inflammation. Nat. Rev. Immunol. 13(3), 159–175. https://doi.org/10.1038/nri3399 (2013).
doi: 10.1038/nri3399 pubmed: 23435331
Yuzhalin, A. E. & Kutikhin, A. G. The rest of interleukins. Interleukins Cancer Biol. Heterog. Role https://doi.org/10.1016/B978-0-12-801121-8.00009-9 (2014).
doi: 10.1016/B978-0-12-801121-8.00009-9
Calandra, T. & Roger, T. Macrophage migration inhibitory factor: A regulator of innate immunity. Nat. Rev. Immunol. 3(10), 791–800. https://doi.org/10.1038/nri1200 (2003).
doi: 10.1038/nri1200 pubmed: 14502271 pmcid: 7097468
Lolis, E. & Bucala, R. Macrophage migration inhibitory factor. Expert Opin. Ther. Tar. 7(2), 153–164. https://doi.org/10.1517/14728222.7.2.153 (2003).
doi: 10.1517/14728222.7.2.153
Lue, H., Kleemann, R., Calandra, T., Roger, T. & Bernhagen, J. Macrophage migration inhibitory factor (MIF): Mechanisms of action and role in disease. Microbes Infect. 4(4), 449–460. https://doi.org/10.1016/s1286-4579(02)01560-5 (2002).
doi: 10.1016/s1286-4579(02)01560-5 pubmed: 11932196
Binder, B. R. et al. Plasminogen activator inhibitor 1: Physiological and pathophysiological roles. News Physiol. Sci. 17, 56–61. https://doi.org/10.1152/nips.01369.2001 (2002).
doi: 10.1152/nips.01369.2001 pubmed: 11909993
Lim, J. H. et al. Tumor suppressor CYLD regulates acute lung injury in lethal Streptococcus pneumoniae infections. Immunity 27(2), 349–360. https://doi.org/10.1016/j.immuni.2007.07.011 (2007).
doi: 10.1016/j.immuni.2007.07.011 pubmed: 17723219
Lim, J. H., Woo, C. H. & Li, J. D. Critical role of type 1 plasminogen activator inhibitor (PAI-1) in early host defense against nontypeable Haemophilus influenzae (NTHi) infection. Biochem. Bioph. Res. Co 414(1), 67–72. https://doi.org/10.1016/j.bbrc.2011.09.023 (2011).
doi: 10.1016/j.bbrc.2011.09.023
Wang, Z. et al. PAI-1 and IFN-gamma in the regulation of innate immune homeostasis during sublethal yersiniosis. Blood Cells Mol. Dis. 50(3), 196–201. https://doi.org/10.1016/j.bcmd.2012.11.005 (2013).
doi: 10.1016/j.bcmd.2012.11.005 pubmed: 23218129
Hyun, J. et al. Human intestinal epithelial cells express interleukin-10 through toll-like receptor 4-mediated epithelial-macrophage crosstalk. J. Innate Immun. 7(1), 87–101. https://doi.org/10.1159/000365417 (2015).
doi: 10.1159/000365417 pubmed: 25171731
Krishnan, M. et al. Molecular mechanism underlying the TLR4 antagonistic and antiseptic activities of papiliocin, an insect innate immune response molecule. P Natl. Acad. Sci. USA https://doi.org/10.1073/pnas.2115669119 (2022).
doi: 10.1073/pnas.2115669119
Zhou, X. Q. et al. Cecropin B represses CYP3A29 expression through activation of the TLR2/4-NF-kappa B/PXR signaling pathway. Sci. Rep. Uk https://doi.org/10.1038/srep27876 (2016).
doi: 10.1038/srep27876
Szalapata, K. et al. Serine protease inhibitors-new molecules for modification of polymeric biomaterials. Biomolecules https://doi.org/10.3390/biom10010082 (2020).
doi: 10.3390/biom10010082 pubmed: 31947983 pmcid: 7023003
Kamiloglu, S., Sari, G., Ozdal, T. & Capanoglu, E. Guidelines for cell viability assays. Food Front. 1(3), 332–349. https://doi.org/10.1002/fft2.44 (2020).
doi: 10.1002/fft2.44
Tarpey, M. M., Wink, D. A. & Grisham, M. B. Methods for detection of reactive metabolites of oxygen and nitrogen: In vitro and in vivo considerations. Am. J. Physiol. Regul. Integr. Comp. Physiol. 286(3), R431–R444. https://doi.org/10.1152/ajpregu.00361.2003 (2004).
doi: 10.1152/ajpregu.00361.2003 pubmed: 14761864

Auteurs

Katarzyna Szałapata (K)

Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka, 19, 20-033, Lublin, Poland.

Mateusz Pięt (M)

Department of Virology and Immunology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033, Lublin, Poland.

Martyna Kasela (M)

Department of Pharmaceutical Microbiology, Medical University of Lublin, Chodzki 1, 20-093, Lublin, Poland.

Marcin Grąz (M)

Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka, 19, 20-033, Lublin, Poland.

Justyna Kapral-Piotrowska (J)

Department of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033, Lublin, Poland.

Aleksandra Mordzińska-Rak (A)

Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka, 19, 20-033, Lublin, Poland.
Department of Biochemistry and Molecular Biology, Medical University of Lublin, Chodzki 1, 20-093, Lublin, Poland.

Elżbieta Samorek (E)

Department of Virology and Immunology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033, Lublin, Poland.
Department of Pharmacology and Toxicology, National Veterinary Research Institute, Pulawy, Poland.

Paulina Pieniądz (P)

Department of Virology and Immunology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033, Lublin, Poland.

Jolanta Polak (J)

Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka, 19, 20-033, Lublin, Poland.

Monika Osińska-Jaroszuk (M)

Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka, 19, 20-033, Lublin, Poland.

Roman Paduch (R)

Department of Virology and Immunology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033, Lublin, Poland.

Bożena Pawlikowska-Pawlęga (B)

Department of Functional Anatomy and Cytobiology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka 19, 20-033, Lublin, Poland.

Anna Malm (A)

Department of Pharmaceutical Microbiology, Medical University of Lublin, Chodzki 1, 20-093, Lublin, Poland.

Anna Jarosz-Wilkołazka (A)

Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Sklodowska University, Akademicka, 19, 20-033, Lublin, Poland. anna.jarosz-wilkolazka@mail.umcs.pl.

Classifications MeSH