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Hypoxic Preconditioning Improved Neuroprotective Effect of Bone Marrow-Mesenchymal Stem Cells Transplantation in Acute Glaucoma Models

DOI: 10.4236/jbise.2016.94018, PP. 245-257

Keywords: Hypoxic Preconditioning, Transplantation, Bone Marrow-Mesenchymal Stem Cells, BM-MSCs, Glaucoma, Neuroprotective

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Abstract:

This study explored the novel strategy of hypoxic preconditioning of Bone Marrow Mesenchymal Stem Cells (BM-MSCs) before intra vitreal transplantation to improve neuroprotective effects of Retinal Ganglion Cells (RGCs) in Acute Glaucoma Models. The methods of this research were isolated mesenchymal stem cells from the bone marrow of adult wild-type Sprague-Dawley (SD) rats. BM-MSCs were cultured under normoxic or hypoxic (1% oxygen for 24 hours) conditions. Normoxic or hypoxic BM-MSCs were transplanted intravitreally 1 week after ocular hypertension induction by acutely increasing IOP to 100 - 120 mmHg for 60 minutes. Rats were killed 4 weeks after transplanted. Apoptosis was examined by tunnel assay and expression Brn3b (Brn3b = RGCs marker) by immunohistochemical analysis of the retina. Results showed that transplantation of hypoxic preconditioning BM-MSCs in acute glaucoma models resulted in a significant apoptosis decreasing (p < 0.05) and an significant increasing in RGCs (p < 0.05), as well as enhanced mor-phologic and functional benefits of stem cell therapy versus normoxic BM-MSCs transplantation. Conclusions: Hypoxic preconditioning enhances the capacity of BM-MSCs transplantation to improve neuroprotective effects of RGCs in Acute Glaucoma Models.

References

[1]  Skuta, G.L., Cantor, L.B. and Weiss, J.S. (2009) Basic and Clinical Science Course Glaucoma. Vol. 2009-2010, Section 10, San Francisco.
[2]  Gupta, N. and Weinreb, R.N. (1997) New Definitions of Glaucoma. Current Opinion in Ophthalmology, 8, 38-41.
http://dx.doi.org/10.1097/00055735-199704000-00007
[3]  Quigley, H.A. (1999) Neuronal Death in Glau-coma. Progress in Retinal and Eye Research, 18, 39-57.
http://dx.doi.org/10.1016/S1350-9462(98)00014-7
[4]  Klein, B.E., Klein, R., Sponsel, W.E., Franke, T., Cantor, L.B., Martone, J., et al. (1992) Prevalence of Glaucoma: The Beaver Dam Eye Study. Ophthalmology, 99, 1499-1504.
http://dx.doi.org/10.1016/S0161-6420(92)31774-9
[5]  Tielsch, J.M., Katz, J., Singh, K., Quigley, H.A., Gottsch, J.D., Javitt, J., et al. (1991) A Population-Based Evaluation of Glaucoma Screening: The Baltimore Eye Survey. American Journal of Epidemiology, 134, 1102-1110.
[6]  Johnson, T.V., Bull, N.D. and Martin, K.R. (2010) Identification of Barriers to Retinal Engraftment of Transplanted Stem Cells. Investigative Ophthalmology & Visual Science, 51, 960-970.
http://dx.doi.org/10.1167/iovs.09-3884
[7]  Malgieri, A., et al. (2010) Bone Marrow and Umbilical Cord Blood Human Mesenchymal Stem Cells: State of the Art. International Journal of Clinical and Experimental Medicine, 3, 248-269.
[8]  Otify, D.Y., Youssef, E.A., Nagy, N.B., Marei, M.K. and Youssif, M.I. (2014) Transdifferentiation of Bone Marrow Mesenchymal Stem Cells into Neural Cells via Cerebrospinal Fluid. Biomedicine and Biotechnology, 2, 66-79.
[9]  Hermann, A., Liebau, S., Gastl, R., Fickert, S., Habisch, H.J., Fiedler, J., Schwarz, J., Brenner, R. and Storch, A. (2006) Comparative Analysis of Neuroectodermal Differentiation Capacity of Human Bone Marrow Stromal Cells Using Various Conversion Protocols. Journal of Neuroscience Research, 83, 1502-1514.
http://dx.doi.org/10.1002/jnr.20840
[10]  Garza, M.T.G. and Cuevas, J.E.M. (2012) Rat Adult Stem Cell Differentiation into Immature Retinal Cells. Stem Cell Discovery, 2, 62-69.
http://dx.doi.org/10.4236/scd.2012.22010
[11]  Bull, N.D., Johnson, T.V. and Martin, K.R. (2008) Stem Cells for Neuroprotection in Glaucoma. Progress in Brain Research, 173, 511-519.
http://dx.doi.org/10.1016/S0079-6123(08)01135-7
[12]  Charalambous, P., Hurst, L.A. and Thanos, S. (2008) Engrafted Chicken Neural Tube-Derived Stem Cells Support the Innate Propensity for Axonal Regeneration within the Rat Optic Nerve. Investigative Ophthalmology & Visual Science, 49, 3513-3524.
http://dx.doi.org/10.1167/iovs.07-1473
[13]  Zhang, Y., Klassen, H.J., Tucker, B.A., Perez, M.T. and Young, M.J. (2007) CNS Progenitor Cells Promote a Permissive Environment for Neurite Outgrowth via a Matrix Metalloproteinase-2-Dependent Mechanism. Journal of Neuroscience, 27, 4499-4506.
http://dx.doi.org/10.1523/JNEUROSCI.0200-07.2007
[14]  Wang, X. (2009) Hsp20-Engineered Mesenchymal Stem Cells Are Resistant to Oxidative Stress via Enhanced Activation of Akt and Increased Secretion of Growth Factors. Wiley Online Library.
[15]  Theus, M.H. (2009) In Vitro Hypoxic Preconditioning of Embryonic Stem Cells as a Strategy of Promoting Cell Survival and Functional Benefits after Transplantation into the Ischemic Rat Brain. Experimental Neurology, 120, 656- 670.
[16]  Hausenloy, D.J. and Yellon, D.M. (2009) Preconditioning and Postconditioning: Underlying Mechanisms and Clinical Application. Atherosclerosis, 204, 334-341.
http://dx.doi.org/10.1016/j.atherosclerosis.2008.10.029
[17]  Hu, X., Yu, S.P., Fraser, J.L., Lu, Z., Ogle, M.E., Wang, J.A. and Wei, L. (2008) Transplantation of Hypoxia-Preconditioned Mesenchymal Stem Cells Improves Infarcted Heart Function via Enhanced Survival of Implanted Cells and Angiogenesis. The Journal of Thoracic and Cardiovascular Surgery, 135, 799-808.
http://dx.doi.org/10.1016/j.jtcvs.2007.07.071
[18]  Yu, S.P., Wei, Z. and Wei, L. (2013) Preconditioning Strategy in Stem Cell Transplantation Therapy. Translational Stroke Research, 4, 76-88.
http://dx.doi.org/10.1007/s12975-012-0251-0
[19]  Wei, L., Fraser, J.L., Yang, L.Z., Hu, X. and Yu, S.P. (2012) Transplantation of Hypoxia Preconditioned Bone Marrow Mesenchymal Stem Cells Enhances Angiogenesis and Neurogenesis after Cerebral Ischemia in Rats. Neurobiology of Disease, 46, 635-645.
http://dx.doi.org/10.1016/j.nbd.2012.03.002
[20]  Tse, W.T., Pendleton, J.D., Beyer, W.M., Egalka, M.C. and Guinan, E.C. (2003) Suppression of Allogeneic T-Cell Proliferation by Human Marrow Stromal Cells: Implications in Transplantation. Transplantation, 75, 389-397.
http://dx.doi.org/10.1097/01.TP.0000045055.63901.A9
[21]  Erecinska, M. and Silver, I.A. (2001) Tissue Oxygen Tension and Brain Sensitivity to Hypoxia. Respiration Physiology, 128, 263-276.
http://dx.doi.org/10.1016/S0034-5687(01)00306-1
[22]  Yu, D.-Y. and Cringle, S.J. (2006) Oxygen Distribution in the Mouse Retina. Investigative Ophthalmology & Visual Science, 47, 1109-1112.
http://dx.doi.org/10.1167/iovs.05-1118
[23]  Grayson, W.L., Zhao, F., Izadpanah, R., Bunnell, B. and Ma, T. (2006) Effects of Hypoxia on Human Mesenchymal Stem Cell Expansion and Plasticity in 3D Constructs. Journal of Cellular Physiology, 207, 331-339.
http://dx.doi.org/10.1002/jcp.20571
[24]  Lee, S.H., Lee, Y.J. and Han, H.J. (2011) Role of Hypoxia-Induced Fibronectin-Integrin β1 Expression in Embryonic Stem Cell Proliferation and Migration: Involvement of PI3K/Akt and FAK. Journal of Cellular Physiology, 226, 484-493.
http://dx.doi.org/10.1002/jcp.22358
[25]  Prado-Lopez, S., Conesa, A., Arminán, A., Martinez-Losa, M., Es-cobedo-Lucea, C., Gandia, C., et al. (2010) Hypoxia Promotes Efficient Differentiation of Human Embryonic Stem Cells to Functional Endothelium. Stem Cells, 28, 407-418.
[26]  Lee, S.H., Suh, H.N., Lee, Y.J., Seo, B.N., Ha, J.W. and Han, H.J. (2012) Midkine Prevented Hypoxic Injury of Mouse Embryonic Stem Cells through Activation of Akt and HIF-1α via Low-Density Lipoprotein Receptor-Related Protein-1. Journal of Cellular Physiology, 227, 1731-1739.
http://dx.doi.org/10.1002/jcp.22897
[27]  Adachi, M., Takahashi, K., Nishikawa, M., Miki, H. and Uyama, M. (1996) High Intraocular Pressure-Induced Ischemia and Reperfusion Injury in the Optic Nerve and Retina in Rat. Graeff’s Archieve for Clinical and Experimental Ophthalmology, 234, 445-451.
http://dx.doi.org/10.1007/BF02539411
[28]  Windisch, B.K., LeVatte, T.L., Archibald, M.L. and Chauhan, B.C. (2009) Induction of Heat Shock Proteins 27 and 72 in Retinal Ganglion Cells after Acute Pressure-Induced Ischaemia. Clinical & Experimental Ophthalmology, 37, 299-307.
[29]  Slater, K., Katie, P., Thomson, J., et al. (2013) Synthetic Peptide Coated Surface for Culture of Human Mesenchymal Stem Cell in a Defined and Xeno-Free Medium. Adult Stem Cell Therapy and Regenerative Medicine, Cleveland Marriott Downtown at Key Center, Cleveland, 19-21 August 2013, 53.
[30]  Xu, W. and Xu, G.X. (2011) Mesenchymal Stem Cells for Retinal Diseases. International Journal of Ophthalmology, 4, 413-421.
[31]  Johnson, T.V., Bull, N.D. and Martin, K.R. (2010) Identification of Barriers to Retinal Engraftment of Transplanted Stem Cells. Investigative Ophthalmology & Visual Science, 51, 960-970.
http://dx.doi.org/10.1167/iovs.09-3884
[32]  Taran, R., Mamidi, M.K., Singh, G., Dutta, S., Parhar, I.S., John, J.P., Bhonde, R., Pal, R. and Das, A.K. (2014) In Vitro and in Vivo Neurogenic Potential of Mesenchymal Stem Cells Isolated from Different Sources. Journal of Biosciences, 39, 157-169.
http://dx.doi.org/10.1007/s12038-013-9409-5
[33]  Zhang, Y. and Wang, W. (2010) Effects of Bone Marrow Mesenchymal Stem Cell Transplantation on Light-Damaged Retina. Investigative Ophthalmology & Visual Science, 51, 3742-3748.
http://dx.doi.org/10.1167/iovs.08-3314
[34]  Hess, D.C. and Borlongan, C.V. (2008) Stem Cells and Neurological Diseases. Cell Proliferation, 41, 94-114.
http://dx.doi.org/10.1111/j.1365-2184.2008.00486.x
[35]  Chen, J., Li, Y., Wang, L., Zhang, Z., Lu, D., Lu, M. and Chopp, M. (2001) Therapeutic Benefit of Intravenous Administration of Bone Marrow Stromal Cells after Cerebral Ischemia in Rats. Stroke, 32, 1005-1011.
http://dx.doi.org/10.1161/01.STR.32.4.1005
[36]  Ogle, M.E., Yu, S.P. and Wei, L. (2009) Primed for Lethal Battle: A Step Forward to Enhance the Efficacy and Efficiency of Stem Cell Transplantation Therapy. The Journal of Thoracic and Cardiovascular Surgery, 138, 527.
http://dx.doi.org/10.1016/j.jtcvs.2009.06.003
[37]  Semenza, G.L. (2011) Hypoxia-Inducible Factor 1: Regulator of Mitochondrial Metabolism and Mediator of Ischemic Preconditioning. Biochimica et Biophysica Acta-Molecular Cell Research, 1813, 1263-1268.
http://dx.doi.org/10.1016/j.bbamcr.2010.08.006
[38]  Chen, X., Li, Y., Wang, L., Katakowski, M., Zhang, L., Chen, J., et al. (2002) Ischemic Rat Brain Extracts Induce Human Marrow Stromal Cell Growth Factor Production. Neuropathology, 22, 275-279.
http://dx.doi.org/10.1046/j.1440-1789.2002.00450.x
[39]  Liu, J., Narasimhan, P., Yu, F. and Chan, P.H. (2005) Neuroprotection by Hypoxic Preconditioning Involves Oxidative Stress-Mediated Expression of Hypoxiainducible Factor and Erythropoietin. Stroke, 36, 1264-1269.
http://dx.doi.org/10.1161/01.STR.0000166180.91042.02
[40]  Danton, G.H. and Dietrich, W.D. (2003) Inflammatory Mechanisms after Ischemia and Stroke. Journal of Neuropathology & Experimental Neurology, 62, 127-136.
http://dx.doi.org/10.1093/jnen/62.2.127
[41]  Hanisch, U.K. (2002) Microglia as a Source and Target of Cytokines. Glia, 40, 140-155.
http://dx.doi.org/10.1002/glia.10161
[42]  Ohmi, K., Greenberg, D.S., Rajavel, K.S., Ryazantsev, S., Li, H.H. and Neufeld, E.F. (2003) Activated Microglia in Cortex of Mouse Models of Mucopolysaccharidoses I and IIIB. Proceedings of the National Academy of Sciences of the United States of America, 100, 1902-1907.
http://dx.doi.org/10.1073/pnas.252784899
[43]  Uchiyama, T., Engelman, R.M., Maulik, N. and Das, D.K. (2004) Role of Akt Signaling in Mitochondrial Survival Pathway Triggered by Hypoxic Preconditioning. Circulation, 109, 3042-3049.
http://dx.doi.org/10.1161/01.CIR.0000130647.29030.90

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