دوره 25، شماره 113 - ( 6-1396 )                   جلد 25 شماره 113 صفحات 68-58 | برگشت به فهرست نسخه ها

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Abdanipour A, Shahsavandi B, Dadkhah M, Alipour M, Feizi H. The Antiapoptotic Effect of Ghrelin in the H2O2 Treated Bone Marrow-Derived Mesenchymal Stem Cells of Rat. J Adv Med Biomed Res 2017; 25 (113) :58-68
URL: http://journal.zums.ac.ir/article-1-4793-fa.html
عبدانی پور علیرضا، شاهسوندی بهناز، دادخواه مسعود، علیپور محسن، فیضی هادی. اثر ضد آپوپتوزی گرلین در سلول‌های بنیادی استرومایی مشتق از مغز استخوان موش صحرایی تیمار شده با پراکسید هیدروژن. Journal of Advances in Medical and Biomedical Research. 1396; 25 (113) :58-68

URL: http://journal.zums.ac.ir/article-1-4793-fa.html


1- دکترای تخصصی علوم تشریح، استادیار گروه علوم تشریح، دانشکده‌ی پزشکی، دانشگاه علوم پزشکی زنجان، زنجان
2- دانشجوی کارشناسی ارشد گروه فیزیولوژی و فارماکولوژی دانشکده‌ی پزشکی، دانشگاه علوم پزشکی زنجان، زنجان
3- دکترای تخصصی فیزیولوژی، استاد گروه فیزیولوژی و فارماکولوژی، دانشکده‌ی پزشکی، دانشگاه علوم پزشکی زنجان، زنجان
4- دکترای تخصصی فیزیولوژی، استادیار گروه فیزیولوژی و فارماکولوژی، دانشکده‌ی پزشکی، دانشگاه علوم پزشکی زنجان، زنجان
5- دانشکده‌ی پزشکی، دانشگاه علوم پزشکی زنجان، زنجان ، hfeizik@zums.ac.ir
چکیده:   (151259 مشاهده)
Background and Objective: Apoptosis is a form of programmed cell death and oxidative stress is one of the factors that lead to apoptosis. Ghrelin is a 28 amino acid peptide and its antiapoptotic effects have been shown previously. The aim of this study was to evaluate the effect of ghrelin on cell survival and apoptosis of rat bone marrow mesenchymal stem cells (BMSCs).
Materials and Methods: BMSCs were cultured as control and H2O2 treated groups with and without different doses of ghrelin (0.1-1-10-100 µM) for 24 and 48 hours. To find out the best dose and time of effect for ghrelin, MTT was used to determine cell survival. BMSC apoptosis rate was detected using the TUNEL technique.
Results: Cultured BMSCs showed that the cells are fibroblastic in appearance and adherent to culture dishes as well as being capable of having a very high proliferation rate. Ghrelin treatment increased proliferation and cell survival in both normal and H2O2 exposed BMSCs. The best dose and time that ghrelin could affect cell proliferation was 100µM and 48 hours respectively. Treatment with ghrelin significantly reduced apoptosis in BMSCs in this dose and time.
Conclusion: Ghrelin treatment causes an increase in BMSCs proliferation and reduction of H2O2 induced apoptosis in these cells.
 
 
متن کامل [PDF 477 kb]   (159690 دریافت)    
نوع مطالعه: کارآزمایی بالینی |
دریافت: 1396/6/4 | پذیرش: 1396/6/4 | انتشار: 1396/6/4

فهرست منابع
1. Wyllie AH, Kerr JFR, Currie AR. Cell death: the significance of apoptosis. Int Rev Cytol. 1980; 68: 251-306. [DOI:10.1016/S0074-7696(08)62312-8]
2. Spencer SL, Sorger PK. Measuring and modeling apoptosis in single cells. center for cell decision processes, department of Systems Biology, Harvard Medical School, Boston, MA 02115; USA.
3. Riedl SJ, Salvesen GS. The apoptosome: signaling platform of cell death. Nat Rev Mol Cell Biol. 2007; 8:405-13. [DOI:10.1038/nrm2153] [PMID]
4. Sies H. Biochemistry of oxidative stress. Angew Chem Int Ed Engl. 1986; 25: 1058-71. [DOI:10.1002/anie.198610581]
5. Lennicke C, Rahn J, Lichtenfels R, Wessjohann LA, Seliger B. Hydrogen peroxide - production, fate and role in redox signaling of tumor cells. Cell Commun Signal. 2015; 13: 39. [DOI:10.1186/s12964-015-0118-6] [PMID] [PMCID]
6. Clement MV, Ponton A, Pervaiz S. Apoptosis induced by hydrogen peroxide is mediated by decreased superoxide anion concentration and reduction of intracellular milieu. FEBSLett. 1998; 440: 13-8. [DOI:10.1016/S0014-5793(98)01410-0]
7. Miller EW, Dickinson BC, Chang CJ. Aquaporin-3 mediates hydrogen peroxide uptake to regulate downstream intracellular signaling. Proc Natl Acad Sci USA. 2010; 107: 15681-86. [DOI:10.1073/pnas.1005776107] [PMID] [PMCID]
8. Beyer Nardi N, da Silva Meirelles L. Mesenchymal Stem Cells: Isolation, In Vitro Expansion and Characterization. Handb Exp Pharmacol. 2006; : 249-82. [DOI:10.1007/3-540-31265-X_11]
9. Zhang F, Wang C, Jing S, et al. Lectin-like oxidized LDL receptor-1 expresses in mouse bone marrow-derived mesenchymal stem cells and stimulates their proliferation. Exp Cell Res. 2013; 319: 1054-1059. [DOI:10.1016/j.yexcr.2013.01.021] [PMID]
10. Farrell MJ, Fisher MB, Huang AH, Shin JI, Farrell KM, Mauck RL. Functional properties of bone marrow-derived MSC-based engineered cartilage are unstable with very long-term in vitro culture. J Biomech. 2014; 47: 2173-82. [DOI:10.1016/j.jbiomech.2013.10.030] [PMID] [PMCID]
11. Xu YQ, Liu ZC. Therapeutic potential of adult bonemarrow stem cells in liver disease and delivery approaches. Stem Cell Rev. 2008; 4: 101-12. [DOI:10.1007/s12015-008-9019-z] [PMID]
12. Pirzad Jahromi G, Shabanzadeh Pirsaraei A, Sadr SS, et al. Multipotent bone marrow stromal cell therapy promotes endogenous cell proliferation following ischemic stroke. Clin Exp Pharmacol Physiol. 2015; 42: 1158-67. [DOI:10.1111/1440-1681.12466] [PMID]
13. CF Peng, XX Tian, J Deng, et al. ASSA14-03-23 CREG over-expression in BMSC protect against myocardial infarction via VHL/HIF-1α/VEGF pathway mediated vascularisation. Heart 2015; 101: A16. [DOI:10.1136/heartjnl-2014-307109.41]
14. Wang S. Clinical applications of mesenchymal stem cells. J Hematol Oncol. 2012; 5. [DOI:10.1186/1756-8722-5-19] [PMID] [PMCID]
15. Zhang F, Ren T, WU J. TGF-β1 induces apoptosis of bone marrow-derived mesenchymal stem cells via regulation of mitochondrial reactive oxygen species production. Exp Ther Med. 2015; 10: 1224-28. [DOI:10.3892/etm.2015.2590] [PMID] [PMCID]
16. Kojima M, Hosoda H, Date Y, Nakazato M, Matsuo H, Kangawa K. Ghrelin is agrowth-hormone-releasingacylated peptide from stomach. Nature. 1999; 402: 656-60. [DOI:10.1038/45230] [PMID]
17. Nanzer AM, Khalaf S, Mozid AM, et al. Ghrelin exerts a proliferative effect on a rat pituitary somatotroph cell line via the mitogen-activated protein kinase pathway. Eur J Endocrinol. 2004; 151: 233-40. [DOI:10.1530/eje.0.1510233] [PMID]
18. Yu H, Xu G, Fan X. The effect of ghrelin on cell proliferation in small intestinal IEC-6 cells. Biomed Pharmacother. 2013; 67: 235-9. [DOI:10.1016/j.biopha.2013.01.007] [PMID]
19. Lee JH, Patel K, Tae HJ, et al. Ghrelin augments murine T-cell proliferation by activation of the phosphatidylinositol-3-kinase, extracellular signal-regulated kinase and protein kinase C signaling pathways. FEBS Lett. 2014; 588: 4708-19. [DOI:10.1016/j.febslet.2014.10.044] [PMID] [PMCID]
20. Nagaya N, Uematsu M, Kojima M, et al. Chronic administration of ghrelin improves left ventricular dysfunction and attenuates development of cardiac cachexia in rats with heart failure. Circulation. 2001; 104: 1430-5. [DOI:10.1161/hc3601.095575] [PMID]
21. Baldanzi G, Filigheddu N, Cutrupi S, et al. Ghrelin and des-acyl ghrelin inhibit cell death in cardiomyocytes and endothelial cells through ERK1/2 and PI 3-kinase/AKT. J Cell Biol. 2002; 159: 1029-37. [DOI:10.1083/jcb.200207165] [PMID] [PMCID]
22. Hwang S, Moon M, Kim S, Hwang L, Ahn KJ, Park S. Neuroprotective effect of ghrelin is associated with decreased expression of
23. prostate apoptosis response-4. Endocr J. 2009; 56: 609-17. [DOI:10.1507/endocrj.K09E-072] [PMID]
24. Yang C, Wang Y, Liu H, et al. Ghrelin protects H9c2 cardiomyocytes from angiotensin II-induced apoptosis through the endoplasmic reticulum stress pathway. J Cardiovasc Pharmacol. 2012; 59: 465-71. [DOI:10.1097/FJC.0b013e31824a7b60] [PMID]
25. Liang QH, LiuY, Wu SS, Cui RR, YuanLQ, Liao EY. Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway. Toxicol Apply Pharmacol. 2013; 272: 591-597. [DOI:10.1016/j.taap.2013.07.018] [PMID]
26. Han D, Huang W, Ma S, et al. Ghrelin improves functional survival of engrafted adipose-derived mesenchymal stem cells in ischemic heart through PI3K/Akt Signaling Pathway. Biomed Res Int. 2015; 2015: 858349. [DOI:10.1155/2015/858349] [PMID] [PMCID]
27. Almasi S, Shahsavandi B, Aliparasti MR, Alipour MR, Rahnama B, Feizi H. The anti- apoptotic effect of ghrelin in the renal tissue of chronic hypoxic rats. Physiol Pharmacol. 2015; 19: 114-20.
28. Kheradmand A, Dezfoulian O, Alirezaei M, RasoulianB. Ghrelin modulates testicular germ cells apoptosis and proliferation in adult normal rats. Biochem Biophys Res Commun. 2012; 419: 299-304. [DOI:10.1016/j.bbrc.2012.02.014] [PMID]
29. Bonfili L, Cuccioloni M, Cecarini V, et al. Ghrelin induces apoptosis in colon adenocarcinoma cells via proteasome inhibition and autophagy induction. Apoptosis. 2013; 18: 1188-200. [DOI:10.1007/s10495-013-0856-0] [PMID]
30. Aliparasti MR, Alipour MR, Almasi S, Feizi H. Ghrelin administration increases the bax/bcl-2 gene expression ratio in the heart of chronic hypoxic rats. Adv Pharm Bull. 2015; 5: 195-99. [DOI:10.15171/apb.2015.027] [PMID] [PMCID]
31. Li B, Zeng M, Zheng H, et al. Effects of ghrelin on the apoptosis of humanneutrophils in vitro. Int J Mol Med. 2016; 38: 794-802. [DOI:10.3892/ijmm.2016.2668] [PMID] [PMCID]
32. Alipour MR, Feizi H, Mohaddes G, Keyhanmanesh R, Khamnei S, Ansarin K, Ebrahimi H: Effect of exogenous ghrelin on body weight and hematocrit of male adult rats in chronic Hypoxia. Int J Endocriol Metab. 2010; 8: 201-205.
33. Cherry YR, Toki J, Asou H, et al. Production of hematopoietic stem cell-chemotactic factor by bone marrow stromal cells. Blood. 1994; 83: 964-71.
34. Guerriero A, Worfard L, Holland HK, Guo GR, Sheehan K, Waller EK. Thrombopoietin is synthesized by bone marrow stromal cells. Blood. 1997; 90: 3444-55. [DOI:10.1182/blood.V90.9.3444]
35. Mehrasa R, Vaziri H, Oodi A, et al. Mesenchymal Stem cells as a feeder layer can prevent apoptosis of expanded hematopoietic stem cells derived from cord blood. Int J Mol cell Med. 2014; 3: 1-10.
36. Dasilva CL, Goncalves R, Crapnell KB, Cabral JM, Zanjani ED, Almeida-porada G. A human stromal-based serum-free cultare system supports the ex vivo expansion/maintenance of bone marrow and cord blood hemtpoict stem/progenitor cells. Exp Hematol. 2005; 33: 828-35. [DOI:10.1016/j.exphem.2005.03.017] [PMID]

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