Rationale for Determining the Functional Potency of Mesenchymal Stem Cells in Preventing Regulated Cell Death for Therapeutic Use

Abderrahim Naji, Narufumi Suganuma, Nicolas Espagnolle, Ken-Ichi Yagyu, Nobuyasu Baba, Luc Sensebé, Frédéric Deschaseaux, Abderrahim Naji, Narufumi Suganuma, Nicolas Espagnolle, Ken-Ichi Yagyu, Nobuyasu Baba, Luc Sensebé, Frédéric Deschaseaux

Abstract

Mesenchymal stem (stromal) cells (MSCs) are being investigated for treating degenerative and inflammatory disorders because of their reparative and immunomodulatory properties. Intricate mechanisms relate cell death processes with immune responses, which have implications for degenerative and inflammatory conditions. We review the therapeutic value of MSCs in terms of preventing regulated cell death (RCD). When cells identify an insult, specific intracellular pathways are elicited for execution of RCD processes, such as apoptosis, necroptosis, and pyroptosis. To some extent, exacerbated RCD can provoke an intense inflammatory response and vice versa. Emerging studies are focusing on the molecular mechanisms deployed by MSCs to ameliorate the survival, bioenergetics, and functions of unfit immune or nonimmune cells. Given these aspects, and in light of MSC actions in modulating cell death processes, we suggest the use of novel functional in vitro assays to ensure the potency of MSCs for preventing RCD. Such analyses should be associated with existing functional assays measuring the anti-inflammatory capabilities of MSCs in vitro. MSCs selected on the basis of two in vitro functional criteria (i.e., prevention of inflammation and RCD) could possess optimal therapeutic efficacy in vivo. In addition, we underline the implications of these perspectives in clinical studies of MSC therapy, with particular focus on acute respiratory distress syndrome. Stem Cells Translational Medicine 2017;6:713-719.

Keywords: Cell death; Cellular therapy; Clinical translation; Degenerative disorder; Functional potency; Inflammatory disorder; Mesenchymal stem cells; Selection technologies.

© 2016 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press.

Figures

Figure 1
Figure 1
Schematic diagram summarizing the concept of MSC selection based on identity and double functional potency for preventing inflammation and RCD before use as therapy. This schematic shows four essential stages, from isolation to release of MSC product for use in clinic. Stage 1: optimal methods for MSC isolation, expansion, and production by GMP with severe control in cell sterility and genetic stability. Stage 2: selection of MSCs based on two criteria, phenotype and potential for differentiation, for assessing MSC “identity” in vitro. Stage 3: selection of MSCs based on two criteria, inhibition of inflammation and inhibition of RCD, for assessing MSC “potency” in vitro. Stage 4: for approval of MSCs for therapy and monitoring of in vivo actions of MSCs. Abbreviations: adipo., adipocytes; CFU‐f, colony‐forming unit fibroblast; chondro., chondroblasts; EC, epithelial cell; FACS, fluorescence‐activated cell sorting; GMP, Good Manufacturing Practices; MΦ, macrophage; MSC, mesenchymal stem (stromal) cell; osteo., osteoblasts; PCR, polymerase chain reaction; RCD, regulated cell death.

References

    1. Kern S, Eichler H, Stoeve J et al. Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue. Stem Cells 2006;24:1294–1301.
    1. Hass R, Kasper C, Böhm S et al. Different populations and sources of human mesenchymal stem cells (MSC): A comparison of adult and neonatal tissue‐derived MSC. Cell Commun Signal 2011;9:12.
    1. Via AG, Frizziero A, Oliva F. Biological properties of mesenchymal stem cells from different sources. Muscles Ligaments Tendons J 2012;2:154–162.
    1. Le Blanc K, Ringdén O. Mesenchymal stem cells: Properties and role in clinical bone marrow transplantation. Curr Opin Immunol 2006;18:586–591.
    1. Galipeau J, Krampera M. The challenge of defining mesenchymal stromal cell potency assays and their potential use as release criteria. Cytotherapy 2015;17:125–127.
    1. Galipeau J, Krampera M, Barrett J et al. International Society for Cellular Therapy perspective on immune functional assays for mesenchymal stromal cells as potency release criterion for advanced phase clinical trials. Cytotherapy 2016;18:151–159.
    1. Dominici M, Le Blanc K, Mueller I et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy 2006;8:315–317.
    1. Ma S, Xie N, Li W et al. Immunobiology of mesenchymal stem cells. Cell Death Differ 2014;21:216–225.
    1. Phinney DG. Functional heterogeneity of mesenchymal stem cells: Implications for cell therapy. J Cell Biochem 2012;113:2806–2812.
    1. Shoshani O, Ravid O, Massalha H et al. Cell isolation induces fate changes of bone marrow mesenchymal cells leading to loss or alternatively to acquisition of new differentiation potentials. Stem Cells 2014;32:2008–2020.
    1. Wagner W, Feldmann RE Jr, Seckinger A et al. The heterogeneity of human mesenchymal stem cell preparations—evidence from simultaneous analysis of proteomes and transcriptomes. Exp Hematol 2006;34:536–548.
    1. Zahorec P, Koller J, Danisovic L et al. Mesenchymal stem cells for chronic wounds therapy. Cell Tissue Bank 2015;16:19–26.
    1. Mineda K, Feng J, Ishimine H et al. Therapeutic potential of human adipose‐derived stem/stromal cell microspheroids prepared by three‐dimensional culture in non‐cross‐linked hyaluronic acid gel. Stem Cells 2015;4:1511–1522.
    1. Samsonraj RM, Rai B, Sathiyanathan P et al. Establishing criteria for human mesenchymal stem cell potency. Stem Cells 2015;33:1878–1891.
    1. Uccelli A, Moretta L, Pistoia V. Mesenchymal stem cells in health and disease. Nat Rev Immunol 2008;8:726–736.
    1. Naji A, Rouas‐Freiss N, Durrbach A et al. Concise review: Combining human leukocyte antigen G and mesenchymal stem cells for immunosuppressant biotherapy. Stem Cells 2013;31:2296–2303.
    1. De Becker A, Riet IV. Homing and migration of mesenchymal stromal cells: How to improve the efficacy of cell therapy?. World J Stem Cells 2016;8:73–87.
    1. Ren G, Chen X, Dong F et al. Concise review: Mesenchymal stem cells and translational medicine: Emerging issues. Stem Cells 2012;1:51–58.
    1. Lee JW, Fang X, Krasnodembskaya A et al. Concise review: Mesenchymal stem cells for acute lung injury: Role of paracrine soluble factors. Stem Cells 2011;29:913–919.
    1. Walter J, Ware LB, Matthay MA. Mesenchymal stem cells: Mechanisms of potential therapeutic benefit in ARDS and sepsis. Lancet Respir Med 2014;2:1016–1026.
    1. Simonson OE, Mougiakakos D, Heldring N et al. In vivo effects of mesenchymal stromal cells in two patients with severe acute respiratory distress syndrome. Stem Cells 2015;4:1199–1213.
    1. Linkermann A, Stockwell BR, Krautwald S et al. Regulated cell death and inflammation: an auto‐amplification loop causes organ failure. Nat Rev Immunol 2014;14:759–767.
    1. Galluzzi L, Bravo‐San Pedro JM, Vitale I et al. Essential versus accessory aspects of cell death: Recommendations of the NCCD 2015. Cell Death Differ 2015;22:58–73.
    1. Tait SW, Ichim G, Green DR. Die another way‐‐non‐apoptotic mechanisms of cell death. J Cell Sci 2014;127:2135–2144.
    1. Kroemer G, Galluzzi L, Vandenabeele P et al.; Nomenclature Committee on Cell Death 2009 . Classification of cell death: Recommendations of the Nomenclature Committee on Cell Death 2009. Cell Death Differ 2009;16:3–11.
    1. Murphy JM, Silke J. Ars Moriendi: The art of dying well—new insights into the molecular pathways of necroptotic cell death. EMBO Rep 2014;15:155–164.
    1. Wallach D, Kang TB, Dillon CP et al. Programmed necrosis in inflammation: Toward identification of the effector molecules. Science 2016;352:aaf2154.
    1. Ashkenazi A, Salvesen G. Regulated cell death: Signaling and mechanisms. Annu Rev Cell Dev Biol 2014;30:337–356.
    1. Galluzzi L, López‐Soto A, Kumar S et al. Caspases connect cell‐death signaling to organismal homeostasis. Immunity 2016;44:221–231.
    1. Poon IK, Lucas CD, Rossi AG et al. Apoptotic cell clearance: Basic biology and therapeutic potential. Nat Rev Immunol 2014;14:166–180.
    1. Medina CB, Ravichandran KS. Do not let death do us part: ‘Find‐me’ signals in communication between dying cells and the phagocytes. Cell Death Differ 2016;23:979–989.
    1. Fullerton JN, Gilroy DW. Resolution of inflammation: A new therapeutic frontier. Nat Rev Drug Discov 2016;15:551–567.
    1. Naji A, Muzembo BA, Yagyu K et al. Endocytosis of indium‐tin‐oxide nanoparticles by macrophages provokes pyroptosis requiring NLRP3‐ASC‐Caspase1 axis that can be prevented by mesenchymal stem cells. Sci Rep 2016;6:26162.
    1. Kong D, Zhu J, Liu Q et al. Mesenchymal stem cells protect neurons against hypoxic‐ischemic injury via inhibiting parthanatos, necroptosis, and apoptosis, but not autophagy. Cell Mol Neurobiol 2016. [Epub ahead of print].
    1. Raffaghello L, Bianchi G, Bertolotto M et al. Human mesenchymal stem cells inhibit neutrophil apoptosis: A model for neutrophil preservation in the bone marrow niche. Stem Cells 2008;26:151–162.
    1. Murphy MB, Moncivais K, Caplan AI. Mesenchymal stem cells: Environmentally responsive therapeutics for regenerative medicine. Exp Mol Med 2013;45:e54.
    1. Ahmad T, Mukherjee S, Pattnaik B et al. Miro1 regulates intercellular mitochondrial transport & enhances mesenchymal stem cell rescue efficacy. EMBO J 2014;33:994–1010.
    1. Islam MN, Das SR, Emin MT et al. Mitochondrial transfer from bone‐marrow‐derived stromal cells to pulmonary alveoli protects against acute lung injury. Nat Med 2012;18:759–765.
    1. Jackson MV, Morrison TJ, Doherty DF et al. Mitochondrial transfer via tunneling nanotubes is an important mechanism by which mesenchymal stem cells enhance macrophage phagocytosis in the in vitro and in vivo models of ARDS. Stem Cells 2016;34:2210–2223.
    1. Vallabhaneni KC, Penfornis P, Dhule S et al. Extracellular vesicles from bone marrow mesenchymal stem/stromal cells transport tumor regulatory microRNA, proteins, and metabolites. Oncotarget 2015;6:4953–4967.
    1. Han J, Kim B, Shin JY et al. Iron oxide nanoparticle‐mediated development of cellular gap junction crosstalk to improve mesenchymal stem cells’ therapeutic efficacy for myocardial infarction. ACS Nano 2015;9:2805–2819.
    1. Wang X, Gerdes HH. Transfer of mitochondria via tunneling nanotubes rescues apoptotic PC12 cells. Cell Death Differ 2015;22:1181–1191.
    1. Cselenyák A, Pankotai E, Horváth EM et al. Mesenchymal stem cells rescue cardiomyoblasts from cell death in an in vitro ischemia model via direct cell‐to‐cell connections. BMC Cell Biol 2010;11:29.
    1. Li N, Sarojini H, An J et al. Prosaposin in the secretome of marrow stroma‐derived neural progenitor cells protects neural cells from apoptotic death. J Neurochem 2010;112:1527–1538.
    1. Kim SY, Lee JH, Kim HJ et al. Mesenchymal stem cell‐conditioned media recovers lung fibroblasts from cigarette smoke‐induced damage. Am J Physiol Lung Cell Mol Physiol 2012;302:L891–L908.
    1. Uzunhan Y, Bernard O, Marchant D et al. Mesenchymal stem cells protect from hypoxia‐induced alveolar epithelial‐mesenchymal transition. Am J Physiol Lung Cell Mol Physiol 2016;310:L439–L451.
    1. Dozmorov I, Eisenbraun MD, Lefkovits I. Limiting dilution analysis: from frequencies to cellular interactions. Immunol Today 2000;21:15–18.
    1. Salem B, Miner S, Hensel NF et al. Quantitative activation suppression assay to evaluate human bone marrow‐derived mesenchymal stromal cell potency. Cytotherapy 2015;17:1675–1686.
    1. Moon HG, Cao Y, Yang J et al. Lung epithelial cell‐derived extracellular vesicles activate macrophage‐mediated inflammatory responses via ROCK1 pathway. Cell Death Dis 2015;6:e2016.
    1. Wilson JG, Liu KD, Zhuo H et al. Mesenchymal stem (stromal) cells for treatment of ARDS: A phase 1 clinical trial. Lancet Respir Med 2015;3:24–32.
    1. Kao KC, Hu HC, Chang CH et al. Diffuse alveolar damage associated mortality in selected acute respiratory distress syndrome patients with open lung biopsy. Crit Care 2015;19:228.
    1. Munneke JM, Spruit MJ, Cornelissen AS et al. The potential of mesenchymal stromal cells as treatment for severe steroid‐refractory acute graft‐versus‐host disease: A critical review of the literature. Transplantation 2015. [Epub ahead of print].
    1. Jouan‐Lanhouet S, Riquet F, Duprez L et al. Necroptosis, in vivo detection in experimental disease models. Semin Cell Dev Biol 2014;35:2–13.
    1. Kaczmarek A, Vandenabeele P, Krysko DV. Necroptosis: The release of damage‐associated molecular patterns and its physiological relevance. Immunity 2013;38:209–223.
    1. Vanden Berghe T, Demon D, Bogaert P et al. Simultaneous targeting of IL‐1 and IL‐18 is required for protection against inflammatory and septic shock. Am J Respir Crit Care Med 2014;189:282–291.

Source: PubMed

3
購読する