Placental Mesenchymal Stromal Cells Rescue Ambulation in Ovine Myelomeningocele

Stem cells translational medicine - Tập 4 Số 6 - Trang 659-669 - 2015
Aijun Wang1, Erin G. Brown1, Lee Lankford1, B Keller1, Christopher D. Pivetti1, Nicole Sitkin1, Michael S. Beattie2, Jacqueline C. Bresnahan2, Diana L. Farmer1
1Surgical Bioengineering Laboratory, Department of Surgery, University of California, Davis, Health System, Sacramento, California, USA
2Brain and Spinal Injury Center, Department of Neurological Surgery, University of California, San Francisco, San Francisco, California, USA

Tóm tắt

Abstract

Myelomeningocele (MMC)—commonly known as spina bifida—is a congenital birth defect that causes lifelong paralysis, incontinence, musculoskeletal deformities, and severe cognitive disabilities. The recent landmark Management of Myelomeningocele Study (MOMS) demonstrated for the first time in humans that in utero surgical repair of the MMC defect improves lower limb motor function, suggesting a capacity for improved neurologic outcomes in this disorder. However, functional recovery was incomplete, and 58% of the treated children were unable to walk independently at 30 months of age. In the present study, we demonstrate that using early gestation human placenta-derived mesenchymal stromal cells (PMSCs) to augment in utero repair of MMC results in significant and consistent improvement in neurologic function at birth in the rigorous fetal ovine model of MMC. In vitro, human PMSCs express characteristic MSC markers and trilineage differentiation potential. Protein array assays and enzyme-linked immunosorbent assay show that PMSCs secrete a variety of immunomodulatory and angiogenic cytokines. Compared with adult bone marrow MSCs, PMSCs secrete significantly higher levels of brain-derived neurotrophic factor and hepatocyte growth factor, both of which have known neuroprotective capabilities. In vivo, functional and histopathologic analysis demonstrated that human PMSCs mediate a significant, clinically relevant improvement in motor function in MMC lambs and increase the preservation of large neurons within the spinal cord. These preclinical results in the well-established fetal ovine model of MMC provide promising early support for translating in utero stem cell therapy for MMC into clinical application for patients.

Significance

This study presents placenta-derived mesenchymal stromal cell (PMSC) treatment as a potential therapy for myelomeningocele (MMC). Application of PMSCs can augment current in utero surgical repair in the well-established and rigorously applied fetal lamb model of MMC. Treatment with human PMSCs significantly and dramatically improved neurologic function and preserved spinal cord neuron density in experimental animals. Sixty-seven percent of the PMSC-treated lambs were able to ambulate independently, with two exhibiting no motor deficits whatsoever. In contrast, none of the lambs treated with the vehicle alone were capable of ambulation. The locomotor rescue demonstrated in PMSC-treated lambs indicates great promise for future clinical trials to improve paralysis in children afflicted with MMC.

Từ khóa


Tài liệu tham khảo

Coran, Expert Consult-Online and Print

Ouyang, 2007, Health care expenditures of children and adults with spina bifida in a privately insured U.S. population, Birth Defects Res A Clin Mol Teratol, 79, 552, 10.1002/bdra.20360

Parker, 2010, Updated national birth prevalence estimates for selected birth defects in the United States, 2004-2006, Birth Defects Res A Clin Mol Teratol, 88, 1008, 10.1002/bdra.20735

Adzick, 2011, A randomized trial of prenatal versus postnatal repair of myelomeningocele, N Engl J Med, 364, 993, 10.1056/NEJMoa1014379

Flake, 2004, In utero stem cell transplantation, Best Pract Res Clin Obstet Gynaecol, 18, 941, 10.1016/j.bpobgyn.2004.06.006

Tiblad, 2008, Fetal stem-cell transplantation, Best Pract Res Clin Obstet Gynaecol, 22, 189, 10.1016/j.bpobgyn.2007.07.007

Liang, 2014, Paracrine mechanisms of mesenchymal stem cell-based therapy: Current status and perspectives, Cell Transplant, 23, 1045, 10.3727/096368913X667709

Guillot, 2007, Human first-trimester fetal MSC express pluripotency markers and grow faster and have longer telomeres than adult MSC, Stem Cells, 25, 646, 10.1634/stemcells.2006-0208

Portmann-Lanz, 2006, Placental mesenchymal stem cells as potential autologous graft for pre- and perinatal neuroregeneration, Am J Obstet Gynecol, 194, 664, 10.1016/j.ajog.2006.01.101

Murphy, 2013, Amniotic fluid and placental membranes: Unexpected sources of highly multipotent cells, Semin Reprod Med, 31, 62, 10.1055/s-0032-1331799

Lankford, 2015, Early gestation chorionic villi-derived stromal cells for fetal tissue engineering, World J Stem Cells, 7, 195, 10.4252/wjsc.v7.i1.195

Lee, 2012, Comparison of immunomodulatory effects of placenta mesenchymal stem cells with bone marrow and adipose mesenchymal stem cells, Int Immunopharmacol, 13, 219, 10.1016/j.intimp.2012.03.024

Calzarossa, 2013, Neurorescue effects and stem properties of chorionic villi and amniotic progenitor cells, Neuroscience, 234, 158, 10.1016/j.neuroscience.2012.12.038

Jones, 2012, Ontological differences in first compared to third trimester human fetal placental chorionic stem cells, PLoS One, 7, e43395, 10.1371/journal.pone.0043395

Roselli, 2013, Fetal mesenchymal stromal cells from cryopreserved human chorionic villi: Cytogenetic and molecular analysis of genome stability in long-term cultures, Cytotherapy, 15, 1340, 10.1016/j.jcyt.2013.06.019

Poloni, 2008, Characterization and expansion of mesenchymal progenitor cells from first-trimester chorionic villi of human placenta, Cytotherapy, 10, 690, 10.1080/14653240802419310

von Koch, 2005, Myelomeningocele: Characterization of a surgically induced sheep model and its central nervous system similarities and differences to the human disease, Am J Obstet Gynecol, 193, 1456, 10.1016/j.ajog.2005.02.110

Meuli, 1997, The spinal cord lesion in human fetuses with myelomeningocele: Implications for fetal surgery, J Pediatr Surg, 32, 448, 10.1016/S0022-3468(97)90603-5

Brown, 2015, Development of a locomotor rating scale for testing motor function in sheep, J Pediatr Surg, 50, 617, 10.1016/j.jpedsurg.2015.01.002

Gensel, 2006, Behavioral and histological characterization of unilateral cervical spinal cord contusion injury in rats, J Neurotrauma, 23, 36, 10.1089/neu.2006.23.36

Delcroix, 2010, EGF and bFGF pre-treatment enhances neural specification and the response to neuronal commitment of MIAMI cells, Differentiation, 80, 213, 10.1016/j.diff.2010.07.001

Dominici, 2006, Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement, Cytotherapy, 8, 315, 10.1080/14653240600855905

Deng, 2006, Mesenchymal stem cells spontaneously express neural proteins in culture and are neurogenic after transplantation, Stem Cells, 24, 1054, 10.1634/stemcells.2005-0370

Nieto, 2002, The snail superfamily of zinc-finger transcription factors, Nat Rev Mol Cell Biol, 3, 155, 10.1038/nrm757

Kim, 2003, SOX10 maintains multipotency and inhibits neuronal differentiation of neural crest stem cells, Neuron, 38, 17, 10.1016/S0896-6273(03)00163-6

Sarkar, 2013, The sox family of transcription factors: Versatile regulators of stem and progenitor cell fate, Cell Stem Cell, 12, 15, 10.1016/j.stem.2012.12.007

Isenmann, 2009, TWIST family of basic helix-loop-helix transcription factors mediate human mesenchymal stem cell growth and commitment, Stem Cells, 27, 2457, 10.1002/stem.181

Yoshizawa, 2003, Fetal surgery for repair of myelomeningocele allows normal development of the rectum in sheep, Pediatr Surg Int, 19, 162, 10.1007/s00383-002-0910-4

Farmer, 2003, In utero repair of myelomeningocele: Experimental pathophysiology, initial clinical experience, and outcomes, Arch Surg, 138, 872, 10.1001/archsurg.138.8.872

Saadai, 2011, Prenatal repair of myelomeningocele with aligned nanofibrous scaffolds—A pilot study in sheep, J Pediatr Surg, 46, 2279, 10.1016/j.jpedsurg.2011.09.014

Saadai, 2013, Human induced pluripotent stem cell-derived neural crest stem cells integrate into the injured spinal cord in the fetal lamb model of myelomeningocele, J Pediatr Surg, 48, 158, 10.1016/j.jpedsurg.2012.10.034

Brown, 2014, In utero repair of myelomeningocele with autologous amniotic membrane in the fetal lamb model, J Pediatr Surg, 49, 133, 10.1016/j.jpedsurg.2013.09.043

Genbacev, 2011, Establishment of human trophoblast progenitor cell lines from the chorion, Stem Cells, 29, 1427, 10.1002/stem.686

Bačenková, 2011, Isolation and basic characterization of human term amnion and chorion mesenchymal stromal cells, Cytotherapy, 13, 1047, 10.3109/14653249.2011.592522

Alfirevic, 2009, Amniocentesis and chorionic villus sampling for prenatal diagnosis, Cochrane Database Syst Review, CD003252

Vellasamy, 2012, Isolation and characterisation of mesenchymal stem cells derived from human placenta tissue, World J Stem Cells, 4, 53, 10.4252/wjsc.v4.i6.53

Meuli, 1995, In utero surgery rescues neurological function at birth in sheep with spina bifida, Nat Med, 1, 342, 10.1038/nm0495-342

Fauza, 2008, Neural stem cell delivery to the spinal cord in an ovine model of fetal surgery for spina bifida, Surgery, 144, 367, 10.1016/j.surg.2008.05.009

Korenromp, 1986, Early fetal leg movements in myelomeningocele, Lancet, 1, 917, 10.1016/S0140-6736(86)91022-6

Adzick, 2012, Fetal surgery for myelomeningocele: Trials and tribulations. Isabella Forshall Lecture, J Pediatr Surg, 47, 273, 10.1016/j.jpedsurg.2011.11.021

Stiefel, 2007, Scanning electron microscopy of fetal murine myelomeningocele reveals growth and development of the spinal cord in early gestation and neural tissue destruction around birth, J Pediatr Surg, 42, 1561, 10.1016/j.jpedsurg.2007.04.019

Barlow, 2008, Comparison of human placenta- and bone marrow-derived multipotent mesenchymal stem cells, Stem Cells Dev, 17, 1095, 10.1089/scd.2007.0154

Hass, 2011, Different populations and sources of human mesenchymal stem cells (MSC): A comparison of adult and neonatal tissue-derived MSC, Cell Commun Signal, 9, 12, 10.1186/1478-811X-9-12

Martinez, 2014, Neurotrauma and mesenchymal stem cells treatment: From experimental studies to clinical trials, World J Stem Cells, 6, 179, 10.4252/wjsc.v6.i2.179

Bussolino, 1992, Hepatocyte growth factor is a potent angiogenic factor which stimulates endothelial cell motility and growth, J Cell Biol, 119, 629, 10.1083/jcb.119.3.629

Ferrara, 2003, The biology of VEGF and its receptors, Nat Med, 9, 669, 10.1038/nm0603-669

Yancopoulos, 2000, Vascular-specific growth factors and blood vessel formation, Nature, 407, 242, 10.1038/35025215

Maina, 1999, Hepatocyte growth factor, a versatile signal for developing neurons, Nat Neurosci, 2, 213, 10.1038/6310

Bai, 2012, Hepatocyte growth factor mediates mesenchymal stem cell–induced recovery in multiple sclerosis models, Nat Neurosci, 15, 862, 10.1038/nn.3109

Lu, 2014, BDNF and synaptic plasticity, cognitive function, and dysfunction, Handbook Exp Pharmacol, 220, 223, 10.1007/978-3-642-45106-5_9

Weishaupt, 2012, BDNF: The career of a multifaceted neurotrophin in spinal cord injury, Exp Neurol, 238, 254, 10.1016/j.expneurol.2012.09.001

Tejima, 2009, Neuroprotective effects of overexpressing tissue inhibitor of metalloproteinase TIMP-1, J Neurotrauma, 26, 1935, 10.1089/neu.2009.0959

Souvenir, 2011, Tissue inhibitor of matrix metalloproteinase-1 mediates erythropoietin-induced neuroprotection in hypoxia ischemia, Neurobiol Dis, 44, 28, 10.1016/j.nbd.2011.05.020

Quertainmont, 2012, Mesenchymal stem cell graft improves recovery after spinal cord injury in adult rats through neurotrophic and pro-angiogenic actions, PLoS ONE, 7, e39500, 10.1371/journal.pone.0039500

Uccelli, 2011, Neuroprotective features of mesenchymal stem cells, Best Pract Res Clin Haematol, 24, 59, 10.1016/j.beha.2011.01.004