DOI QR코드

DOI QR Code

Lactoferrin Protects Human Mesenchymal Stem Cells from Oxidative Stress-Induced Senescence and Apoptosis

  • Park, Soon Yong (Department of Biological Science, Dong-A University) ;
  • Jeong, Ae-Jin (Department of Biological Science, Dong-A University) ;
  • Kim, Geun-Young (Jeju National Quarantine Station, Centers for Disease Control & Prevention) ;
  • Jo, Ara (Department of Biological Science, Dong-A University) ;
  • Lee, Joo Eon (Department of Biological Science, Dong-A University) ;
  • Leem, Sun-Hee (Department of Biological Science, Dong-A University) ;
  • Yoon, Joung-Hahn (Department of Mathematics, Dong-A University) ;
  • Ye, Sang Kyu (Department of Pharmacology and Biomedical Sciences, College of Medicine, Seoul National University) ;
  • Chung, Jin Woong (Department of Biological Science, Dong-A University)
  • Received : 2017.07.17
  • Accepted : 2017.09.01
  • Published : 2017.10.28

Abstract

Mesenchymal stem cells (MSCs) have been suggested as a primary candidate for cell therapy applications because they have self-renewal and differentiation capabilities. Although they can be expanded in ex vivo system, clinical application of these cells is still limited because they survive poorly and undergo senescence or apoptosis when transplanted and exposed to environmental factors such as oxidative stress. Thus, reducing oxidative stress is expected to improve the efficacy of MSC therapy. The milk protein lactoferrin is a multifunctional iron-binding glycoprotein that plays various roles, including reduction of oxidative stress. Thus, we explored the effect of lactoferrin on oxidative stress-induced senescence and apoptosis of human MSCs (hMSCs). Measurement of reactive oxygen species (ROS) revealed that lactoferrin inhibited the production of hydrogen peroxide-induced intracellular ROS, suggesting lactoferrin as a good candidate as an antioxidant in hMSCs. Pretreatment of lactoferrin suppressed hydrogen peroxide-induced senescence of hMSCs. In addition, lactoferrin reduced hydrogen peroxide-induced apoptosis via inhibition of caspase-3 and Akt activation. These results demonstrate that lactoferrin can be a promising factor to protect hMSCs from oxidative stress-induced senescence and apoptosis, thus increasing the efficacy of MSC therapy.

Keywords

References

  1. Uccelli A, Moretta L, Pistoia V. 2008. Mesenchymal stem cells in health and disease. Nat. Rev. Immunol. 8: 726-736. https://doi.org/10.1038/nri2395
  2. Colter DC, Class R, DiGirolamo CM, Prockop DJ. 2009. Rapid expansion of recycling stem cells in cultures of plastic-adherent cells from human bone marrow. Proc. Natl. Acad. Sci. USA 97: 3213-3218.
  3. da Silva Meirelles L, Chagastellse PC, Nardi NB. 2006. Mesenchymal stem cells reside in virtually all post-natal organs and tissues. J. Cell Sci. 119: 2204-2213. https://doi.org/10.1242/jcs.02932
  4. Lee MW, Yang MS, Park JS, Kim HC, Kim YJ, Choi J. 2005. Isolation of mesenchymal stem cells from cryopreserved human umbilical cord blood. Int. J. Hematol. 81: 126-130. https://doi.org/10.1532/IJH97.A10404
  5. Sekiya I, Larson BL, Smith JR, Pochampally R, Cui JG, Prockop DJ. 2002. Expansion of human adult stem cells from bone marrow stroma: conditions that maximize the yields of early progenitors and evaluate their quality. Stem Cells 20: 530-541. https://doi.org/10.1634/stemcells.20-6-530
  6. Kotobuki N, Hirose M, Takakura Y, Ohgushi H. 2004. Cultured autologous human cells for hard tissue regeneration: preparation and characterization of mesenchymal stem cells from bone marrow. Artif. Organs 28: 33-39. https://doi.org/10.1111/j.1525-1594.2004.07320.x
  7. Bang OY, Lee JS, Lee PH, Lee G. 2005. Autologous mesenchymal stem cell transplantation in stroke patients. Ann. Neurol. 57: 874-882. https://doi.org/10.1002/ana.20501
  8. Chen SL, Fang WW, Ye F, Liu YH, Qian J, Shan SJ, et al. 2004. Effect on left ventricular function of intracoronary transplantation of autologous bone marrow mesenchymal stem cell in patients with acute myocardial infarction. Am. J. Cardiol. 94: 92-95. https://doi.org/10.1016/j.amjcard.2004.03.034
  9. Parekkadan B, Milwid JM. 2010. Mesenchymal stem cells as therapeutics. Annu. Rev. Biomed. Eng. 12: 87-117. https://doi.org/10.1146/annurev-bioeng-070909-105309
  10. Alekseenko LL, Zemelko VI, Domnina AP, Lyublinskaya OG, Zenin VV, Pugovkina NA, et al. 2014. Sublethal heat shock induces premature senescence rather than apoptosis in human mesenchymal stem cells. Cell Stress Chaperones 19: 355-366. https://doi.org/10.1007/s12192-013-0463-6
  11. Zhu W, Chen J, Cong X, Hu S, Chen X. 2006. Hypoxia and serum deprivation-induced apoptosis in mesenchymal stem cells. Stem Cells 24: 416-425. https://doi.org/10.1634/stemcells.2005-0121
  12. Brandl A, Meyer M, Bechmann V, Nerlich M, Angele P. 2011. Oxidative stress induces senescence in human mesenchymal stem cells. Exp. Cell Res. 317: 1541-1547. https://doi.org/10.1016/j.yexcr.2011.02.015
  13. Burova E, Borodkina A, Shatrova A, Nikolsky N. 2013. Sublethal oxidative stress induces the premature senescence of human mesenchymal stem cells derived from endometrium. Oxid. Med. Cell Longev. 2013: 474931.
  14. Rodrigues M, Turner O, Stolz D, Griffith LG, Wells A. 2012. Production of reactive oxygen species by multipotent stromal cells/mesenchymal stem cells upon exposure to fas ligand. Cell Transplant. 21: 2171-2187. https://doi.org/10.3727/096368912X639035
  15. Legrand D , Pierce A , El ass E, C arpentier M, M aril ler C , Mazurier J. 2008. Lactoferrin structure and functions. Adv. Exp. Med. Biol. 606: 163-194.
  16. Ward PP, Paz E, Conneely OM. 2005. Multifunctional roles of lactoferrin: a critical overview. Cell. Mol. Life Sci. 62: 2540-2548. https://doi.org/10.1007/s00018-005-5369-8
  17. Kruzel ML, Actor JK, Radak Z, Bacsi A, Saavedra-Molina A, Boldogh I. 2010. Lactoferrin decreases LPS-induced mitochondrial dysfunction in cultured cells and in animal endotoxemia model. Innate Immun. 16: 67-79. https://doi.org/10.1177/1753425909105317
  18. Kruzel ML, Bacsi A, Choudhury B, Sur S, Boldogh I. 2006. Lactoferrin decreases pollen antigen-induced allergic airway inflammation in a murine model of asthma. Immunology 119: 159-166. https://doi.org/10.1111/j.1365-2567.2006.02417.x
  19. Safaeian L, Zabolian H. 2014. Antioxidant effects of bovine lactoferrin on dexamethasone-induced hypertension in rat. ISRN Pharmacol. 2014: 943523.
  20. Yagi H, Tan J, Tuan RS. 2013. Polyphenols suppress hydrogen peroxide-induced oxidative stress in human bone-marrow derived mesenchymal stem cells. J. Cell. Biochem. 114: 1163-1173. https://doi.org/10.1002/jcb.24459
  21. Chen QM. 2000. Replicative senescence and oxidant-induced premature senescence. Beyond the control of cell cycle checkpoints. Ann NY Acad Sci. 908: 111-125.
  22. Mohammadzadeh M, Halabian R, Gharehbaghian A, Amirizadeh N, Jahanian-Najafabadi A, Roushandeh AM, Roudhenar MH. 2012. Nrf-2 overexpression in mesenchymal stem cells reduces oxidative stress-induced apoptosis and cytotoxicity. Cell Stress Chaperones 17: 553-565. https://doi.org/10.1007/s12192-012-0331-9
  23. Kennedy A L, M orton J P, M anoharan I , Nel son DM, Jamieson NB, Pawlikowski JS, et al. 2011. Activation of the PIK3CA/AKT pathway suppresses senescence induced by an activated RAS oncogene to promote tumorigenesis. Mol. Cell 42: 36-49. https://doi.org/10.1016/j.molcel.2011.02.020
  24. Brunet A, Bonni A, Zigmond MJ, Lin MZ, Juo P, Hu LS, et al. 1999. Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor. Cell 96: 857-868. https://doi.org/10.1016/S0092-8674(00)80595-4
  25. Xu X, Lu Z, Qiang W, Vidimar V, Kong B, Kim JJ, Wei JJ. 2014. Inactivation of AKT induces cellular senescence in uterine leiomyoma. Endocrinology 155: 1510-1519. https://doi.org/10.1210/en.2013-1929
  26. Grey A, Zhu Q, Watson M, Callon K, Cornish J. 2006. Lactoferrin potently inhibits osteoblast apoptosis, via an LRP1-independent pathway. Mol. Cell. Endocrinol. 251: 96-102. https://doi.org/10.1016/j.mce.2006.03.002
  27. Sussman M. 2007. "AKT"ing lessons for stem cells: regulation of cardiac myocyte and progenitor cell proliferation. Trends Cardiovasc. Med. 17: 235-240. https://doi.org/10.1016/j.tcm.2007.08.003
  28. Devasagayam T, Tilak JC, Boloor KK, Sane KS, Ghaskadbi SS, Lele RD. 2004. Free radicals and antioxidants in human health: current status and future prospects. J. Assoc. Physicians India 52: 796-804.
  29. Nogueira V, Park Y, Chen CC, Xu PZ, Chen ML, Tonic I, et al. 2008. Akt determines replicative senescence and oxidative or oncogenic premature senescence and sensitizes cells to oxidative apoptosis. Cancer Cell 14: 458-470. https://doi.org/10.1016/j.ccr.2008.11.003
  30. Sanchez L, Calvo M, Brock JH. 1992. Biological role of lactoferrin. Arch. Dis. Child. 67: 657-661. https://doi.org/10.1136/adc.67.5.657
  31. Kelly GS. 2003. Bovine colostrums: a review of clinical uses. Altern. Med. Rev. 8: 378-394.
  32. Struff WG, Sprotte G. 2008. Bovine colostrum as a biologic in clinical medicine: a review - Part II: clinical s tudies. Int. J. Clin. Pharmacol. Ther. 46: 211-225. https://doi.org/10.5414/CPP46211
  33. Garcia-Montoya IA, Cendon TS, Arevalo-Gallegos S, Rascon-Cruz Q. 2012. Lactoferrin a multiple bioactive protein: an overview. Biochim. Biophys. Acta 1820: 226-236. https://doi.org/10.1016/j.bbagen.2011.06.018
  34. Park YG, Jeong JK, Lee JH, Lee YJ, Seol JW, Kim SJ, et al. 2013. Lactoferrin protects against prion protein-induced cell death in neuronal cells by preventing mitochondrial dysfunction. Int. J. Mol. Med. 31: 325-330. https://doi.org/10.3892/ijmm.2012.1198

Cited by

  1. Oxidative Stress and Necrotizing Enterocolitis: Pathogenetic Mechanisms, Opportunities for Intervention, and Role of Human Milk vol.2018, pp.None, 2017, https://doi.org/10.1155/2018/7397659
  2. Aloe-Emodin Induces Endoplasmic Reticulum Stress-Dependent Apoptosis in Colorectal Cancer Cells vol.24, pp.None, 2017, https://doi.org/10.12659/msm.908400
  3. Comparison of Oxidative Stress Effects on Senescence Patterning of Human Adult and Perinatal Tissue-Derived Stem Cells in Short and Long-term Cultures vol.15, pp.13, 2017, https://doi.org/10.7150/ijms.27181
  4. Intestinal health benefits of bovine whey proteins after simulated gastrointestinal digestion vol.49, pp.None, 2017, https://doi.org/10.1016/j.jff.2018.08.043
  5. Phenotypic and transcriptomic characterization of canine myeloid-derived suppressor cells vol.9, pp.None, 2017, https://doi.org/10.1038/s41598-019-40285-3
  6. Effect of Lactoferrin on the Expression Profiles of Long Non-coding RNA during Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells vol.20, pp.19, 2017, https://doi.org/10.3390/ijms20194834
  7. Human Mesenchymal Stem Cell Response to Lactoferrin-based Composite Coatings vol.12, pp.20, 2017, https://doi.org/10.3390/ma12203414
  8. Lactoferrin level in maternal serum is related to birth anthropometry - an evidence for an indirect biomarker of intrauterine homeostasis? vol.32, pp.24, 2017, https://doi.org/10.1080/14767058.2018.1481040
  9. Lactoferrin in Bone Tissue Regeneration vol.27, pp.6, 2017, https://doi.org/10.2174/0929867326666190503121546
  10. Vaginal Lactoferrin Administration Decreases Oxidative Stress in the Amniotic Fluid of Pregnant Women: An Open-Label Randomized Pilot Study vol.7, pp.None, 2017, https://doi.org/10.3389/fmed.2020.00555
  11. Mesenchymal Stem Cell Senescence and Rejuvenation: Current Status and Challenges vol.8, pp.None, 2017, https://doi.org/10.3389/fcell.2020.00364
  12. Molecular Mechanisms Contributing to Mesenchymal Stromal Cell Aging vol.10, pp.2, 2020, https://doi.org/10.3390/biom10020340
  13. Senescent mesenchymal stem/stromal cells and restoring their cellular functions vol.12, pp.9, 2020, https://doi.org/10.4252/wjsc.v12.i9.966
  14. Protective effect of nutraceutical food on the intestinal mucosa of juvenile pacu Piaractus mesopotamicus under high stocking density vol.28, pp.5, 2017, https://doi.org/10.1007/s10499-020-00570-9
  15. Senescent Mesenchymal Stem Cells: Disease Mechanism and Treatment Strategy vol.6, pp.4, 2017, https://doi.org/10.1007/s40610-020-00141-0
  16. A comparative study on the cellular stressors in mesenchymal stem cells (MSCs) and pancreatic β-cells under hyperglycemic milieu vol.476, pp.1, 2017, https://doi.org/10.1007/s11010-020-03922-4
  17. Modulation of fracture healing by the transient accumulation of senescent cells vol.10, pp.None, 2021, https://doi.org/10.7554/elife.69958
  18. Comparative effect of bovine buttermilk, whey, and lactoferrin on the innate immunity receptors and oxidative status of intestinal epithelial cells vol.99, pp.1, 2017, https://doi.org/10.1139/bcb-2020-0121
  19. Complex Interactions in Regulation of Haematopoiesis-An Unexplored Iron Mine vol.12, pp.8, 2017, https://doi.org/10.3390/genes12081270
  20. Epigenetic Clock and Circadian Rhythms in Stem Cell Aging and Rejuvenation vol.11, pp.11, 2017, https://doi.org/10.3390/jpm11111050
  21. Ameliorative effect of recombinant human lactoferrin on the premature ovarian failure in rats after cyclophosphamide treatments vol.14, pp.None, 2017, https://doi.org/10.1186/s13048-020-00763-z
  22. Lactoferrin Alleviated AFM1-Induced Apoptosis in Intestinal NCM 460 Cells through the Autophagy Pathway vol.11, pp.1, 2017, https://doi.org/10.3390/foods11010023