The Combined Effect of Lumenato and Ceramide in the Protection of Collagen Damage Induced by Neutrophils in Normal Human Dermal Fibroblasts — Oak Academic Publishing
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The Combined Effect of Lumenato and Ceramide in the Protection of Collagen Damage Induced by Neutrophils in Normal Human Dermal Fibroblasts
Immunology and Infectious Diseases Laboratory, Department of Clinical Biochemistry and Pharmacology, Faculty of Health Sciences, Ben-Gurion University of The Negev, Beer-Sheva, Israel
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Immunology and Infectious Diseases Laboratory, Department of Clinical Biochemistry and Pharmacology, Faculty of Health Sciences, Ben-Gurion University of The Negev, Beer-Sheva, Israel
1 Immunology and Infectious Diseases Laboratory, Department of Clinical Biochemistry and Pharmacology, Faculty of Health Sciences, Ben-Gurion University of The Negev, Beer-Sheva, Israel
2 Immunology and Infectious Diseases Laboratory, Department of Clinical Biochemistry and Pharmacology, Faculty of Health Sciences, Ben-Gurion University of The Negev, Beer-Sheva, Israel
Introduction : Collagen is the primary structural protein fibroblasts produce in the skin’s extracellular matrix. Infiltration of neutrophils into the epidermis and dermis by exposure to UV causes collagen damage and contributes to photoaging. Methods : To study the combined effect of Lumenato and ceramide in preventing collagen-1 damage induced by phagocytes, we used co-cultures o f normal human dermal fibroblasts (fibroblasts) and activate d human neutrophils. The present study aimed to determine the protective effect of the combination of Lumenato and ceramide on fibroblast collagen-1 damage induced by neutrophils. Results: Lumenato (in the range of 6.5 - 208 μg/ml) or ceramide (in the range of 0.1 - 50 μM) inhibited the production of superoxides and MPO by TNF α -stimulated neutrophils, as well as the production of NO by LPS-stimulated macrophages in a dose-dependent manner. The combinations of Lumenato and ceramide, in low concentrations, caused synergis tic prevention of fibroblasts’ collagen-1 damage induced by TNF α -activate d n eutrophils, detected by fluorescence immunostaining and WB analys is. MPO activity in the supernatants of the co-cultures was also synergistically inhibited. Adding Lumenato or ceramide singly or in combinations in these low concentrations to the fibroblast cultures did not affect the expression of collagen-1. The combinations of Lumenato or ceramide in these concentrations al so caused a synergistic inhibition of NO production by activated macro phages. Conclusions : The results suggest that combining low concentrations o f Lumenato and ceramide results in synergistic protection against fibro blasts’ collagen-1 damage induced by neutrophils, thus indicating their possible potential for enhanced skin health.
Quan, T. and Fisher, G.J. (2015) Role of Age-Associated Alterations of the Dermal Extracellular Matrix Microenvironment in Human Skin Aging: A Mini-Review. Gerontology, 61, 427-434. https://pubmed.ncbi.nlm.nih.gov/25660807/ https://doi.org/10.1159/000371708
Rhie, G., Shin, M.H., Seo, J.Y., Choi, W.W., Cho, K.H., Kim, K.H., Park, K.C., Eun, H.C. and Chung, J.H. (2001) Aging- and Photoaging-Dependent Changes of Enzymic and Nonenzymic Antioxidants in the Epidermis and Dermis of Human Skin in Vivo. Journal of Investigative Dermatology, 117, 1212-1217. https://pubmed.ncbi.nlm.nih.gov/11710935/ https://doi.org/10.1046/j.0022-202x.2001.01469.x
Smith, L.T., Holbrook, K.A. and Madri, J.A. (1986) Collagen Types I, III, and V in Human Embryonic and Fetal Skin. American Journal of Anatomy, 175, 507-521. http://www.ncbi.nlm.nih.gov/pubmed/3521252 https://doi.org/10.1002/aja.1001750409
Kim, H.H., Cho, S., Lee, S., Kim, K.H., Cho, K.H., Eun, H.C. and Chung, J.H. (2006) Photoprotective and Anti-Skin-Aging Effects of Eicosapentaenoic Acid in Human Skin in Vivo. Journal of Lipid Research, 47, 921-930. http://www.ncbi.nlm.nih.gov/pubmed/16467281 https://doi.org/10.1194/jlr.M500420-JLR200
Wlaschek, M., Tantcheva-Poor, I., Naderi, L., Ma, W., Schneider, L.A., Razi-Wolf, Z., Schuller, J. and Scharffetter-Kochanek, K. (2001) Solar UV Irradiation and Dermal Photoaging. Journal of Photochemistry and Photobiology B: Biology, 63, 41-51. https://doi.org/10.1016/S1011-1344(01)00201-9
Yan, W., Zhang, L.L., Yan, L., Zhang, F., Yin, N.B., Lin, H.B., Huang, C.Y., Wang, L., Yu, J., Wang, D.M. and Zhao, Z.M. (2013) Transcriptome Analysis of Skin Photoaging in Chinese Females Reveals the Involvement of Skin Homeostasis and Metabolic Changes. PLOS ONE, 8, e61946. http://www.ncbi.nlm.nih.gov/pubmed/23637934 https://doi.org/10.1371/journal.pone.0061946
Wood, L.C., Elias, P.M., Calhoun, C., Tsai, J.C., Grunfeld, C. and Feingold, K.R. (1996) Barrier Disruption Stimulates Interleukin-1 α Expression and Release from a Pre-Formed Pool in Murine Epidermis. The Journal of Investigative Dermatology, 106, 397-403. http://www.ncbi.nlm.nih.gov/pubmed/8648167 https://doi.org/10.1111/1523-1747.ep12343392
Kawaguchi, Y., Tanaka, H., Okada, T., Konishi, H., Takahashi, M., Ito, M. and Asai, J. (1996) The Effects of Ultraviolet A and Reactive Oxygen Species on the mRNA Expression of 72-kDa Type IV Collagenase and Its Tissue Inhibitor in Cultured Human Dermal Fibroblasts. Archives of Dermatological Research, 288, 39-44. http://www.ncbi.nlm.nih.gov/pubmed/8750933 https://doi.org/10.1007/BF02505041
Gonzalez, S. and Pathak, M.A. (1996) Inhibition of Ultraviolet-Induced Formation of Reactive Oxygen Species, Lipid Peroxidation, Erythema and Skin Photosensitization by Polypodium Leucotomos. Photodermatology, Photoimmunology & Photomedicine, 12, 45-56. http://www.ncbi.nlm.nih.gov/pubmed/8897589 https://doi.org/10.1111/j.1600-0781.1996.tb00175.x
Hruza, L.L. and Pentland, A.P. (1993) Mechanisms of UV-Induced Inflammation. Journal of Investigative Dermatology, 100, 35S-41S. http://www.ncbi.nlm.nih.gov/pubmed/8423392 https://doi.org/10.1111/1523-1747.ep12355240
Bielenberg, D.R., Bucana, C.D., Sanchez, R., Donawho, C.K., Kripke, M.L. and Fidler, I.J. (1998) Molecular Regulation of UVB-Induced Cutaneous Angiogenesis. Journal of Investigative Dermatology, 111, 864-872. http://www.ncbi.nlm.nih.gov/pubmed/9804351 https://doi.org/10.1046/j.1523-1747.1998.00378.x
Rijken, F. and Bruijnzeel, P.L. (2009) The Pathogenesis of Photoaging: The Role of Neutrophils and Neutrophil-Derived Enzymes. Journal of Investigative Dermatology Symposium Proceedings, 14, 67-72. https://pubmed.ncbi.nlm.nih.gov/19675558/ https://doi.org/10.1038/jidsymp.2009.15
Rijken, F. and Bruijnzeel-Koomen, C.A. (2011) Photoaged Skin: The Role of Neutrophils, Preventive Measures, and Potential Pharmacological Targets. Clinical Pharmacology & Therapeutics, 89, 120-124. https://pubmed.ncbi.nlm.nih.gov/21107312/ https://doi.org/10.1038/clpt.2010.221
Rijken, F., Kiekens, R.C. and Bruijnzeel, P.L. (2005) Skin-Infiltrating Neutrophils following Exposure to Solar-Simulated Radiation Could Play an Important Role in Photoageing of Human Skin. British Journal of Dermatology, 152, 321-328. http://www.ncbi.nlm.nih.gov/pubmed/15727646 https://doi.org/10.1111/j.1365-2133.2004.06335.x
Weiss, S.J. (1989) Tissue Destruction by Neutrophils. The New England Journal of Medicine, 320, 365-376. https://www.nejm.org/doi/full/10.1056/NEJM198902093200606 https://doi.org/10.1056/NEJM198902093200606
Monboisse, J.C. and Borel, J.P. (1992) Oxidative Damage to Collagen. In: Emerit, I. and Chance, B., Eds., Free Radicals and Aging, Birkhäuser Basel, Basel, 323-327. https://pubmed.ncbi.nlm.nih.gov/1333311/ https://doi.org/10.1007/978-3-0348-7460-1_32
Solomonov, Y., Hadad, N., Pikovsky, O. and Levy, R. (2021) Lumenato Protects Normal Human Dermal Fibroblasts from Neutrophil-Induced Collagen-3 Damage in Co-Cultures. PLOS ONE, 16, e0248183. http://www.ncbi.nlm.nih.gov/pubmed/33730073 https://doi.org/10.1371/journal.pone.0248183
Hadad, N. and Levy, R. (2012) The Synergistic Anti-Inflammatory Effects of Lycopene, Lutein, β-Carotene, and Carnosic Acid Combinations via Redox-Based Inhibition of NF-κB Signaling. Free Radical Biology and Medicine, 53, 1381-1391. https://pubmed.ncbi.nlm.nih.gov/22889596/ https://doi.org/10.1016/j.freeradbiomed.2012.07.078
Levy, R., Malech, H.L. and Rotrosen, D. (1990) Production of Myeloid Cell Cytosols Functionally and Immunochemically Deficient in the 47 kDa or 67 kDa NADPH Oxidase Cytosolic Factors. Biochemical and Biophysical Research Communications, 170, 1114-1120. https://pubmed.ncbi.nlm.nih.gov/2167670/ https://doi.org/10.1016/0006-291X(90)90508-K
Solomonov, Y., Hadad, N. and Levy, R. (2018) The Combined Anti-Inflammatory Effect of Astaxanthin, Lyc-O-Mato and Carnosic Acid in Vitro and in Vivo in a Mouse Model of Peritonitis. Journal of Nutrition & Food Sciences, 8, Article ID: 1000653. https://doi.org/10.4172/2155-9600.1000653 https://doi.org/10.4172/2155-9600.1000653
Bashir, M.M., Sharma, M.R. and Werth, V.P. (2009) TNF-α Production in the Skin. Archives of Dermatological Research, 301, 87-91. http://www.ncbi.nlm.nih.gov/pubmed/18825399 https://doi.org/10.1007/s00403-008-0893-7
Gaggini, M., Pingitore, A. and Vassalle, C. (2021) Plasma Ceramides Pathophysiology, Measurements, Challenges, and Opportunities. Metabolites, 11, Article 719. http://www.ncbi.nlm.nih.gov/pubmed/34822377 https://doi.org/10.3390/metabo11110719
Nakamura, T., Abe, A., Balazovich, K.J., Wu, D., Suchard, S.J., Boxer, L.A. and Shayman, J.A. (1994) Ceramide Regulates Oxidant Release in Adherent Human Neutrophils. The Journal of Biological Chemistry, 269, 18384-18389. http://www.ncbi.nlm.nih.gov/pubmed/8034585 https://doi.org/10.1016/S0021-9258(17)32319-0
Wong, K., Li, X.B. and Hunchuk, N. (1995) N-Acetylsphingosine (C2--Ceramide) Inhibited Neutrophil Superoxide Formation and Calcium Influx. Journal of Biological Chemistry, 270, 3056-3062. http://www.ncbi.nlm.nih.gov/pubmed/7852386 https://doi.org/10.1074/jbc.270.7.3056
Harty, M.W., Muratore, C.S., Papa, E.F., Gart, M.S., Ramm, G.A., Gregory, S.H. and Tracy Jr., T.F. (2010) Neutrophil Depletion Blocks Early Collagen Degradation in Repairing Cholestatic Rat Livers. The American Journal of Pathology, 176, 1271-1281. http://www.ncbi.nlm.nih.gov/pubmed/20110408 https://doi.org/10.2353/ajpath.2010.090527
Li, Q., Fukuda, K., Lu, Y., Nakamura, Y., Chikama, T., Kumagai, N. and Nishida, T. (2003) Enhancement by Neutrophils of Collagen Degradation by Corneal Fibroblasts. Journal of Leukocyte Biology, 74, 412-419. http://www.ncbi.nlm.nih.gov/pubmed/12949245 https://doi.org/10.1189/jlb.0801757
Chowdhury, S.R., Mh Busra, M.F., Lokanathan, Y., Ng, M.H., Law, J.X., Cletus, U.C. and Binti Haji Idrus, R. (2018) Collagen Type I: A Versatile Biomaterial. Advances in Experimental Medicine and Biology, 1077, 389-414. http://www.ncbi.nlm.nih.gov/pubmed/30357700 https://doi.org/10.1007/978-981-13-0947-2_21
Talwar, H.S., Griffiths, C.E., Fisher, G.J., Hamilton, T.A. and Voorhees, J.J. (1995) Reduced Type I and Type III Procollagens in Photodamaged Adult Human Skin. Journal of Investigative Dermatology, 105, 285-290. http://www.ncbi.nlm.nih.gov/pubmed/7543550 https://doi.org/10.1111/1523-1747.ep12318471
Nakabo, Y. and Pabst, M.J. (1997) C2-Ceramide and C6-Ceramide Inhibited Priming for Enhanced Release of Superoxide in Monocytes, But Had No Effect on the Killing of Leukaemic Cells by Monocytes. Immunology, 90, 477-482. http://www.ncbi.nlm.nih.gov/pubmed/9176098 https://doi.org/10.1046/j.1365-2567.1997.d01-2189.x
Sethi, G. and Sodhi, A. (2004) In Vitro Activation of Murine Peritoneal Macrophages by Ultraviolet B Radiation: Upregulation of CD18, Production of NO, Proinflammatory Cytokines and a Signal Transduction Pathway. Molecular Immunology, 40, 1315-1323. http://www.ncbi.nlm.nih.gov/pubmed/15072850 https://doi.org/10.1016/j.molimm.2004.01.001
Philips, N., Tuason, M., Chang, T., Lin, Y., Tahir, M. and Rodriguez, S.G. (2009) Differential Effects of Ceramide on Cell Viability and Extracellular Matrix Remodeling in Keratinocytes and Fibroblasts. Skin Pharmacology and Physiology, 22, 151-157. http://www.ncbi.nlm.nih.gov/pubmed/19276645 https://doi.org/10.1159/000208168
Coderch, L., Lopez, O., De La Maza, A. and Parra, J.L. (2003) Ceramides and Skin Function. American Journal of Clinical Dermatology, 4, 107-129. http://www.ncbi.nlm.nih.gov/pubmed/12553851 https://doi.org/10.2165/00128071-200304020-00004
Andrieu-Abadie, N., Gouaze, V., Salvayre, R. and Levade, T. (2001) Ceramide in Apoptosis Signaling: Relationship with Oxidative Stress. Free Radical Biology and Medicine, 31, 717-728. http://www.ncbi.nlm.nih.gov/pubmed/11557309 https://doi.org/10.1016/S0891-5849(01)00655-4
Geilen, C.C., Wieder, T. and Orfanos, C.E. (1997) Ceramide Signalling: Regulatory role in Cell Proliferation, Differentiation and Apoptosis in Human Epidermis. Archives of Dermatological Research, 289, 559-566. http://www.ncbi.nlm.nih.gov/pubmed/9373714 https://doi.org/10.1007/s004030050240
Hannun, Y.A. (1994) The Sphingomyelin Cycle and the Second Messenger Function of Ceramide. Journal of Biological Chemistry, 269, 3125-3128. http://www.ncbi.nlm.nih.gov/pubmed/8106344 https://doi.org/10.1016/S0021-9258(17)41834-5
Hannun, Y.A. and Obeid, L.M. (2008) Principles of Bioactive Lipid Signalling: Lessons from Sphingolipids. Nature Reviews Molecular Cell Biology, 9, 139-150. http://www.ncbi.nlm.nih.gov/pubmed/18216770 https://doi.org/10.1038/nrm2329
Obeid, L.M. and Hannun, Y.A. (1995) Ceramide: A Stress Signal and Mediator of Growth Suppression and Apoptosis. Journal of Cellular Biochemistry, 58, 191-198. http://www.ncbi.nlm.nih.gov/pubmed/7673327 https://doi.org/10.1002/jcb.240580208
Okazaki, T., Bielawska, A., Bell, R.M. and Hannun, Y.A. (1990) Role of Ceramide as a Lipid Mediator of 1 α, 25-Dihydroxyvitamin D3-Induced HL-60 Cell Differentiation. Journal of Biological Chemistry, 265, 15823-15831. http://www.ncbi.nlm.nih.gov/pubmed/2394750 https://doi.org/10.1016/S0021-9258(18)55472-7
Zerbinati, N., Sommatis, S., Maccario, C., Di Francesco, S., Capillo, M.C., Grimaldi, G., Rauso, R., Herrera, M., Bencini, P.L. and Mocchi, R. (2021) A Practical Approach for the in Vitro Safety and Efficacy Assessment of an Anti-Ageing Cosmetic Cream Enriched with Functional Compounds. Molecules, 26, Article 7592. http://www.ncbi.nlm.nih.gov/pubmed/34946675 https://doi.org/10.3390/molecules26247592
Britton, G. (1995) Structure and Properties of Carotenoids in Relation to Function. The FASEB Journal, 9, 1551-1558. https://pubmed.ncbi.nlm.nih.gov/8529834/ https://doi.org/10.1096/fasebj.9.15.8529834
Gabrielska, J. and Gruszecki, W.I. (1996) Zeaxanthin (Dihydroxy-β-Carotene) But Not β-Carotene Rigidifies lipiD Membranes: A 1H-NMR Study of Carotenoid-Egg Phosphatidylcholine Liposomes. Biochimica et Biophysica Acta (BBA)—Biomembranes, 1285, 167-174. http://www.ncbi.nlm.nih.gov/pubmed/8972700 https://doi.org/10.1016/S0005-2736(96)00152-6
Singh, S., Banerjee, O., Bhattacharjee, A., Prasad, S.K., Bose, A., Maji, B.K. and Mukherjee, S. (2020) Effect of Individual and Combined Supplementation of Phytoene, Phytofluene, and Lycopene against Nicotine-Induced Pancreatic Islet celL Dysfunction. Toxicology and Environmental Health Sciences, 12, 11-22. https://doi.org/10.1007/s13530-020-00035-9