Systemic administration of clinical-grade multilineage-differentiating stress-enduring cells ameliorates hypoxic–ischemic brain injury in neonatal rats
暂无分享,去创建一个
Atsuto Onoda | Yoshiaki Sato | M. Dezawa | S. Shimizu | M. Mizuno | Kazuto Ueda | K. Irie | Yuta Yamashita | Haruka Mimatsu | Ryosuke Miura | Yuma Kitase | Shoji Go | Masahiro Hayakawa | Toshihiko Suzuki | Masahiro Tsuji | Kenichi Mishima | Yoshiyuki Takahashi
[1] A. Malhotra,et al. Umbilical Cord Blood-Derived Cell Therapy for Perinatal Brain Injury: A Systematic Review & Meta-Analysis of Preclinical Studies , 2022, bioRxiv.
[2] M. Ando,et al. Safety and tolerability of a multilineage-differentiating stress-enduring cell-based product in neonatal hypoxic-ischaemic encephalopathy with therapeutic hypothermia (SHIELD trial): a clinical trial protocol open-label, non-randomised, dose-escalation trial , 2022, BMJ Open.
[3] G. Schmitt,et al. The benefits, limitations and opportunities of preclinical models for neonatal drug development , 2022, Disease models & mechanisms.
[4] K. Abe,et al. Non-Tumorigenic Pluripotent Reparative Muse Cells Provide a New Therapeutic Approach for Neurologic Diseases , 2021, Cells.
[5] M. Akiyama,et al. Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study , 2021, Journal of the European Academy of Dermatology and Venereology : JEADV.
[6] H. Iida,et al. Intravenously delivered multilineage-differentiating stress enduring cells dampen excessive glutamate metabolism and microglial activation in experimental perinatal hypoxic ischemic encephalopathy , 2020, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[7] K. Abe,et al. Therapeutic benefit of Muse cells in a mouse model of amyotrophic lateral sclerosis , 2020, Scientific Reports.
[8] K. Nishigaki,et al. Safety and Efficacy of Human Muse Cell-Based Product for Acute Myocardial Infarction in a First-in-Human Trial. , 2020, Circulation journal : official journal of the Japanese Circulation Society.
[9] T. Tominaga,et al. Intravenously Transplanted Human Multilineage-Differentiating Stress-Enduring Cells Afford Brain Repair in a Mouse Lacunar Stroke Model , 2019, Stroke.
[10] H. Lv,et al. Neonatal hypoxic–ischemic encephalopathy: emerging therapeutic strategies based on pathophysiologic phases of the injury , 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.
[11] M. Iino,et al. Rescue from Stx2-Producing E. coli-Associated Encephalopathy by Intravenous Injection of Muse Cells in NOD-SCID Mice , 2019, Molecular therapy : the journal of the American Society of Gene Therapy.
[12] P. Sanberg,et al. May the force be with you: Transfer of healthy mitochondria from stem cells to stroke cells , 2018, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[13] M. Tsuji,et al. Intravenous Administration of Bone Marrow-Derived Mesenchymal Stem Cell, but not Adipose Tissue-Derived Stem Cell, Ameliorated the Neonatal Hypoxic-Ischemic Brain Injury by Changing Cerebral Inflammatory State in Rat , 2018, Front. Neurol..
[14] Thomas K. Watanabe. A Review of Stem Cell Therapy for Acquired Brain Injuries and Neurodegenerative Central Nervous System Diseases , 2018, PM & R : the journal of injury, function, and rehabilitation.
[15] Y. Chang,et al. Hypothermia broadens the therapeutic time window of mesenchymal stem cell transplantation for severe neonatal hypoxic ischemic encephalopathy , 2018, Scientific reports.
[16] M. Dezawa,et al. Human Multilineage-differentiating Stress-Enduring Cells Exert Pleiotropic Effects to Ameliorate Acute Lung Ischemia–Reperfusion Injury in a Rat Model , 2018, Cell transplantation.
[17] C. Muramatsu,et al. S1P–S1PR2 Axis Mediates Homing of Muse Cells Into Damaged Heart for Long-Lasting Tissue Repair and Functional Recovery After Acute Myocardial Infarction , 2018, Circulation research.
[18] Y. Kondo,et al. Beneficial Effects of Systemically Administered Human Muse Cells in Adriamycin Nephropathy. , 2017, Journal of the American Society of Nephrology : JASN.
[19] G. van Echten-Deckert,et al. Sphingosine 1-phosphate - A double edged sword in the brain. , 2017, Biochimica et biophysica acta. Biomembranes.
[20] F. Motoi,et al. Human Muse Cells, Nontumorigenic Phiripotent-Like Stem Cells, Have Liver Regeneration Capacity through Specific Homing and Cell Replacement in a Mouse Model of Liver Fibrosis , 2017, Cell transplantation.
[21] B. Tatlı,et al. Neonatal hypoxic ischemic encephalopathy: an update on disease pathogenesis and treatment , 2017, Expert review of neurotherapeutics.
[22] K. Nakanishi,et al. Rat umbilical cord blood cells attenuate hypoxic–ischemic brain injury in neonatal rats , 2017, Scientific Reports.
[23] K. Nakanishi,et al. Dedifferentiated Fat Cells as a Novel Source for Cell Therapy to Target Neonatal Hypoxic-Ischemic Encephalopathy , 2017, Developmental Neuroscience.
[24] T. Tominaga,et al. Human Muse Cells Reconstruct Neuronal Circuitry in Subacute Lacunar Stroke Model , 2017, Stroke.
[25] M. Dezawa. Muse Cells Provide the Pluripotency of Mesenchymal Stem Cells: Direct Contribution of Muse Cells to Tissue Regeneration , 2016, Cell transplantation.
[26] C. Svendsen,et al. Regenerative cellular therapies for neurologic diseases , 2016, Brain Research.
[27] Steven P. Miller,et al. Rodent Hypoxia–Ischemia Models for Cerebral Palsy Research: A Systematic Review , 2016, Front. Neurol..
[28] K. Ohno,et al. Neuroprotective potential of molecular hydrogen against perinatal brain injury via suppression of activated microglia. , 2016, Free radical biology & medicine.
[29] H. Mushiake,et al. Transplantation of Unique Subpopulation of Fibroblasts, Muse Cells, Ameliorates Experimental Stroke Possibly via Robust Neuronal Differentiation , 2016, Stem cells.
[30] John H. Zhang,et al. Neuroprotective Strategies after Neonatal Hypoxic Ischemic Encephalopathy , 2015, International journal of molecular sciences.
[31] P. Walczak,et al. The Dark Side of the Force – Constraints and Complications of Cell Therapies for Stroke , 2015, Front. Neurol..
[32] H. Moore,et al. Therapeutic Hypothermia and Hypoxia-Ischemia in the Term-equivalent Neonatal Rat: Characterization of a Translational Pre-clinical Model , 2015, Pediatric Research.
[33] Hye Soo Yoo,et al. Hypothermia Augments Neuroprotective Activity of Mesenchymal Stem Cells for Neonatal Hypoxic-Ischemic Encephalopathy , 2015, PloS one.
[34] K. Blomgren,et al. Administration of Umbilical Cord Blood Cells Transiently Decreased Hypoxic-Ischemic Brain Injury in Neonatal Rats , 2015, Developmental Neuroscience.
[35] A. Kurisaki,et al. Therapeutic Potential of Adipose‐Derived SSEA‐3‐Positive Muse Cells for Treating Diabetic Skin Ulcers , 2015, Stem cells translational medicine.
[36] Tomohiko Nakamura,et al. Incidence and prediction of outcome in hypoxic–ischemic encephalopathy in Japan , 2014, Pediatrics international : official journal of the Japan Pediatric Society.
[37] K. Blomgren,et al. Brain development in rodents and humans: Identifying benchmarks of maturation and vulnerability to injury across species , 2013, Progress in Neurobiology.
[38] S. Auvin,et al. Comparison of Brain Maturation among Species: An Example in Translational Research Suggesting the Possible Use of Bumetanide in Newborn , 2013, Front. Neurol..
[39] K. Blomgren,et al. Grafting of neural stem and progenitor cells to the hippocampus of young, irradiated mice causes gliosis and disrupts the granule cell layer , 2013, Cell Death and Disease.
[40] M. Dezawa,et al. Regenerative Effects of Mesenchymal Stem Cells: Contribution of Muse Cells, a Novel Pluripotent Stem Cell Type that Resides in Mesenchymal Cells , 2012, Cells.
[41] Shabari Tipnis,et al. Radiolabeling of umbilical cord-derived mesenchymal stem cells for in vivo tracking. , 2012, Cancer biotherapy & radiopharmaceuticals.
[42] J. Volpe,et al. Neonatal encephalopathy: An inadequate term for hypoxic–ischemic encephalopathy , 2012, Annals of neurology.
[43] William A Catterall,et al. Autistic behavior in Scn1a+/− mice and rescue by enhanced GABAergic transmission , 2012, Nature.
[44] K. Polderman,et al. Is therapeutic hypothermia immunosuppressive? , 2012, Critical Care.
[45] S. Czasch,et al. Proliferative and Nonproliferative Lesions of the Rat and Mouse Central and Peripheral Nervous Systems , 2012, Toxicologic pathology.
[46] Y. Fujiyoshi,et al. Multilineage-differentiating stress-enduring (Muse) cells are a primary source of induced pluripotent stem cells in human fibroblasts , 2011, Proceedings of the National Academy of Sciences.
[47] Nadia Badawi,et al. Epidemiology of neonatal encephalopathy and hypoxic-ischaemic encephalopathy. , 2010, Early human development.
[48] A. Inutsuka,et al. Unique multipotent cells in adult human mesenchymal cell populations , 2010, Proceedings of the National Academy of Sciences.
[49] Andrew Whitelaw,et al. Neurological outcomes at 18 months of age after moderate hypothermia for perinatal hypoxic ischaemic encephalopathy: synthesis and meta-analysis of trial data , 2010, BMJ : British Medical Journal.
[50] A. Oohira,et al. Chondroitin sulfate, a major niche substance of neural stem cells, and cell transplantation therapy of neurodegeneration combined with niche modification. , 2009, Current stem cell research & therapy.
[51] K. Nakanishi,et al. Reduction of Brain Injury in Neonatal Hypoxic—Ischemic Rats by Intracerebroventricular Injection of Neural Stem/Progenitor Cells Together With Chondroitinase ABC , 2008, Reproductive Sciences.
[52] William Oh,et al. Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy. , 2005, The New England journal of medicine.
[53] C. Ober,et al. HLA‐G and immune tolerance in pregnancy , 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[54] Xuezhi Sun,et al. Ectopic neurons in the hippocampus may be a cause of learning disability after prenatal exposure to X-rays in rats. , 2004, Journal of radiation research.
[55] M. Johnston,et al. Apoptosis Has a Prolonged Role in the Neurodegeneration after Hypoxic Ischemia in the Newborn Rat , 2000, The Journal of Neuroscience.
[56] T. Schallert,et al. CNS plasticity and assessment of forelimb sensorimotor outcome in unilateral rat models of stroke, cortical ablation, parkinsonism and spinal cord injury , 2000, Neuropharmacology.
[57] R. Morris. Developments of a water-maze procedure for studying spatial learning in the rat , 1984, Journal of Neuroscience Methods.
[58] S. Papson,et al. “Model” , 1981 .
[59] J. Rice,et al. The influence of immaturity on hypoxic‐ischemic brain damage in the rat , 1981, Annals of neurology.
[60] F. Ebaugh,et al. The use of radioactive chromium 51 as an erythrocyte tagging agent for the determination or red cell survival in vivo. , 1953, The Journal of clinical investigation.
[61] S. Gray,et al. Determination of the circulating red cell volume in man by radioactive chromium. , 1950, The Journal of clinical investigation.
[62] M. Dezawa,et al. Muse Cells Are Endogenous Reparative Stem Cells. , 2018, Advances in experimental medicine and biology.
[63] Stephen Ashwal,et al. Comparison of Two Neonatal Ischemic Injury Models Using Magnetic Resonance Imaging , 2007, Pediatric Research.
[64] G. Paxinos,et al. The Rat Brain in Stereotaxic Coordinates , 1983 .