Comparative analysis of neuroectodermal differentiation capacity of human bone marrow stromal cells using various conversion protocols

Human adult bone marrow‐derived mesodermal stromal cells (hMSCs) are able to differentiate into multiple mesodermal tissues, including bone and cartilage. There is evidence that these cells are able to break germ layer commitment and differentiate into cells expressing neuroectodermal properties. There is still debate about whether this results from cell fusion, aberrant marker gene expression or real neuroectodermal differentiation. Here we extend our work on neuroectodermal conversion of adult hMSCs in vitro by evaluating various epigenetic conversion protocols using quantitative RT‐PCR and immunocytochemistry. Undifferentiated hMSCs expressed high levels of fibronectin as well as several neuroectodermal genes commonly used to characterize neural cell types, such as nestin, β‐tubulin III, and GFAP, suggesting that hMSCs retain the ability to differentiate into neuroectodermal cell types. Protocols using a direct differentiation of hMSCs into a neural phenotype failed to induce significant changes in morphology and/or expression of markers of early and mature glial/neuronal cells types. In contrast, a multistep protocol with conversion of hMSCs into a neural stem cell‐like population and subsequent terminal differentiation in mature glia and neurons generated relevant morphological changes as well as significant increase of expression levels of marker genes for early and late neural cell types, such as nestin, neurogenin2, MBP, and MAP2ab, accompanied by a loss of their mesenchymal properties. Our data provide an impetus for differentiating hMSCs in vitro into mature neuroectodermal cells. Neuroectodermally converted hMSCs may therefore ultimately help in treating acute and chronic neurodegenerative diseases. Analysis of marker gene expression for characterization of neural cells derived from MSCs has to take into account that several early and late neuroectodermal genes are already expressed in undifferentiated MSCs. © 2006 Wiley‐Liss, Inc.

[1]  V. Silani,et al.  Neuro-glial differentiation of human bone marrow stem cells in vitro , 2005, Experimental Neurology.

[2]  M. Tuszynski,et al.  Can bone marrow-derived stem cells differentiate into functional neurons? , 2005, Experimental Neurology.

[3]  H. Lerche,et al.  Efficient generation of neural stem cell-like cells from adult human bone marrow stromal cells , 2004, Journal of Cell Science.

[4]  L. Lagneaux,et al.  Bone marrow-derived mesenchymal stem cells already express specific neural proteins before any differentiation. , 2004, Differentiation; research in biological diversity.

[5]  Gianluca Gallo,et al.  Reevaluation of in vitro differentiation protocols for bone marrow stromal cells: Disruption of actin cytoskeleton induces rapid morphological changes and mimics neuronal phenotype , 2004, Journal of neuroscience research.

[6]  M. Tuszynski,et al.  Induction of bone marrow stromal cells to neurons: Differentiation, transdifferentiation, or artifact? , 2004, Journal of neuroscience research.

[7]  P. Schiller,et al.  Marrow-isolated adult multilineage inducible (MIAMI) cells, a unique population of postnatal young and old human cells with extensive expansion and differentiation potential , 2004, Journal of Cell Science.

[8]  Mari Dezawa,et al.  Specific induction of neuronal cells from bone marrow stromal cells and application for autologous transplantation. , 2004, The Journal of clinical investigation.

[9]  I. Black,et al.  Adult Bone Marrow Stromal Cells in the Embryonic Brain: Engraftment, Migration, Differentiation, and Long-Term Survival , 2004, The Journal of Neuroscience.

[10]  R. Pochampally,et al.  Serum deprivation of human marrow stromal cells (hMSCs) selects for a subpopulation of early progenitor cells with enhanced expression of OCT-4 and other embryonic genes. , 2004, Blood.

[11]  H. Fine,et al.  Cellular and genetic characterization of human adult bone marrow-derived neural stem-like cells: a potential antiglioma cellular vector. , 2003, Cancer research.

[12]  R. Brenner,et al.  Identification, quantification and isolation of mesenchymal progenitor cells from osteoarthritic synovium by fluorescence automated cell sorting. , 2003, Osteoarthritis and cartilage.

[13]  A. Straube,et al.  Expression of Neuronal Markers in Differentiated Marrow Stromal Cells and CD133+ Stem-Like Cells , 2003, Cell transplantation.

[14]  Klaus Pfeffer,et al.  Fusion of bone-marrow-derived cells with Purkinje neurons, cardiomyocytes and hepatocytes , 2003, Nature.

[15]  Helen M. Blau,et al.  Stable reprogrammed heterokaryons form spontaneously in Purkinje neurons after bone marrow transplant , 2003, Nature Cell Biology.

[16]  Mikael Svensson,et al.  Stem cells from the adult human brain develop into functional neurons in culture. , 2003, Experimental cell research.

[17]  D. Henderson,et al.  Neuroectodermal differentiation from mouse multipotent adult progenitor cells , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[18]  B. Novitch,et al.  Vertebrate neurogenesis is counteracted by Sox1–3 activity , 2003, Nature Neuroscience.

[19]  B. Seshi,et al.  Multilineage gene expression in human bone marrow stromal cells as evidenced by single-cell microarray analysis. , 2003, Blood cells, molecules & diseases.

[20]  G. Comi,et al.  Neuronal generation from somatic stem cells: current knowledge and perspectives on the treatment of acquired and degenerative central nervous system disorders. , 2003, Current gene therapy.

[21]  Kenji F. Tanaka,et al.  Preservation of hematopoietic properties in transplanted bone marrow cells in the brain , 2003, Journal of neuroscience research.

[22]  D. Bodine,et al.  Bone marrow stem cells regenerate infarcted myocardium , 2003, Pediatric transplantation.

[23]  K. Black,et al.  Generation of Neural Progenitor Cells from Whole Adult Bone Marrow , 2002, Experimental Neurology.

[24]  I. Sekiya,et al.  Expansion of Human Adult Stem Cells from Bone Marrow Stroma: Conditions that Maximize the Yields of Early Progenitors and Evaluate Their Quality , 2002, Stem cells.

[25]  C. Pan,et al.  In Vitro Differentiation of Size‐Sieved Stem Cells into Electrically Active Neural Cells , 2002, Stem cells.

[26]  I. Black,et al.  Adult bone marrow stromal stem cells express germline, ectodermal, endodermal, and mesodermal genes prior to neurogenesis , 2002, Journal of neuroscience research.

[27]  I. Weissman,et al.  Little Evidence for Developmental Plasticity of Adult Hematopoietic Stem Cells , 2002, Science.

[28]  C. Robertson,et al.  Failure of bone marrow cells to transdifferentiate into neural cells in vivo. , 2002, Science.

[29]  C. Verfaillie,et al.  Multipotent progenitor cells can be isolated from postnatal murine bone marrow, muscle, and brain. , 2002, Experimental hematology.

[30]  Fred H. Gage,et al.  Astroglia induce neurogenesis from adult neural stem cells , 2002, Nature.

[31]  A. Manira,et al.  Marrow stromal cells form guiding strands in the injured spinal cord and promote recovery , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[32]  C. Verfaillie,et al.  Purification and ex vivo expansion of postnatal human marrow mesodermal progenitor cells. , 2001, Blood.

[33]  S. Tapscott,et al.  NeuroD Homologue Expression During Cortical Development in the Human Brain , 2001, Journal of child neurology.

[34]  J Kohyama,et al.  Brain from bone: efficient "meta-differentiation" of marrow stroma-derived mature osteoblasts to neurons with Noggin or a demethylating agent. , 2001, Differentiation; research in biological diversity.

[35]  G. Kopen,et al.  MicroSAGE Analysis of 2,353 Expressed Genes in a Single Cell‐Derived Colony of Undifferentiated Human Mesenchymal Stem Cells Reveals mRNAs of Multiple Cell Lineages , 2001, Stem cells.

[36]  M. Migita,et al.  Differentiation of transplanted bone marrow cells in the adult mouse brain. , 2001, Transplantation.

[37]  M. Entman,et al.  Regeneration of ischemic cardiac muscle and vascular endothelium by adult stem cells. , 2001, The Journal of clinical investigation.

[38]  Neil D. Theise,et al.  Multi-Organ, Multi-Lineage Engraftment by a Single Bone Marrow-Derived Stem Cell , 2001, Cell.

[39]  I. Black,et al.  Adult rat and human bone marrow stromal stem cells differentiate into neurons. , 2001, Blood cells, molecules & diseases.

[40]  M. Gulisano,et al.  Otx genes in brain morphogenesis , 2001, Progress in Neurobiology.

[41]  Mara Riminucci,et al.  Bone Marrow Stromal Stem Cells: Nature, Biology, and Potential Applications , 2001, Stem cells.

[42]  David M. Bodine,et al.  Bone marrow cells regenerate infarcted myocardium , 2001, Nature.

[43]  I. Fischer,et al.  In vitro differentiation of human marrow stromal cells into early progenitors of neural cells by conditions that increase intracellular cyclic AMP. , 2001, Biochemical and biophysical research communications.

[44]  M. Nieto,et al.  Neural bHLH Genes Control the Neuronal versus Glial Fate Decision in Cortical Progenitors , 2001, Neuron.

[45]  J. Johnson,et al.  Neurogenin2 expression in ventral and dorsal spinal neural tube progenitor cells is regulated by distinct enhancers. , 2001, Developmental biology.

[46]  S. Mckercher,et al.  Turning blood into brain: cells bearing neuronal antigens generated in vivo from bone marrow. , 2000, Science.

[47]  H. Blau,et al.  From marrow to brain: expression of neuronal phenotypes in adult mice. , 2000, Science.

[48]  Xin Wang,et al.  Purified hematopoietic stem cells can differentiate into hepatocytes in vivo , 2000, Nature Medicine.

[49]  M Chopp,et al.  Spinal cord injury in rat: treatment with bone marrow stromal cell transplantation , 2000, Neuroreport.

[50]  I. Black,et al.  Adult rat and human bone marrow stromal cells differentiate into neurons , 2000, Journal of neuroscience research.

[51]  W. Janssen,et al.  Adult Bone Marrow Stromal Cells Differentiate into Neural Cells in Vitro , 2000, Experimental Neurology.

[52]  H. Schöler,et al.  Oct‐4: Control of totipotency and germline determination , 2000, Molecular reproduction and development.

[53]  H. Okano,et al.  Musashi1: An Evolutionally Conserved Marker for CNS Progenitor Cells Including Neural Stem Cells , 2000, Developmental Neuroscience.

[54]  Sunil Badve,et al.  Derivation of hepatocytes from bone marrow cells in mice after radiation‐induced myeloablation , 2000, Hepatology.

[55]  R. Mulligan,et al.  Dystrophin expression in the mdx mouse restored by stem cell transplantation , 1999, Nature.

[56]  D J Prockop,et al.  Marrow stromal cells migrate throughout forebrain and cerebellum, and they differentiate into astrocytes after injection into neonatal mouse brains. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[57]  W. Mars,et al.  Bone marrow as a potential source of hepatic oval cells. , 1999, Science.

[58]  D. Dawson,et al.  Targeting of marrow-derived astrocytes to the ischemic brain. , 1999, Neuroreport.

[59]  W. Huttner,et al.  Expression of the antiproliferative gene TIS21 at the onset of neurogenesis identifies single neuroepithelial cells that switch from proliferative to neuron-generating division. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[60]  Jonas Frisén,et al.  Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System , 1999, Cell.

[61]  A. Simeone Otx1 and Otx2 in the development and evolution of the mammalian brain , 1998, The EMBO journal.

[62]  R. Lovell-Badge,et al.  A role for SOX1 in neural determination. , 1998, Development.

[63]  G Cossu,et al.  Muscle regeneration by bone marrow-derived myogenic progenitors. , 1998, Science.

[64]  Takayuki Asahara,et al.  Isolation of Putative Progenitor Endothelial Cells for Angiogenesis , 1997, Science.

[65]  E. Cartwright,et al.  Embryonic expression of the chicken Sox2, Sox3 and Sox11 genes suggests an interactive role in neuronal development , 1995, Mechanisms of Development.

[66]  U. Lendahl,et al.  Nestin mRNA expression correlates with the central nervous system progenitor cell state in many, but not all, regions of developing central nervous system. , 1995, Brain research. Developmental brain research.

[67]  Elena Cattaneo,et al.  Proliferation and differentiation of neuronal stem cells regulated by nerve growth factor , 1990, Nature.

[68]  R. McKay,et al.  CNS stem cells express a new class of intermediate filament protein , 1990, Cell.

[69]  J. Carson,et al.  Expression and Localization of Myelin Basic Protein in Oligodendrocytes and Transfected Fibroblasts , 1988, Journal of neurochemistry.

[70]  N. Kulagina,et al.  Fibroblast precursors in normal and irradiated mouse hematopoietic organs. , 1976, Experimental hematology.

[71]  Catherine M. Verfaillie,et al.  Pluripotency of mesenchymal stem cells derived from adult marrow , 2007, Nature.

[72]  K. Turksen,et al.  Isolation and characterization , 2006 .

[73]  L. Kanz,et al.  Heterogeneity among human bone marrow-derived mesenchymal stem cells and neural progenitor cells. , 2003, Haematologica.

[74]  M. Valk,et al.  Transplanted bone marrow generates new neurons in human brains , 2003 .

[75]  P. Rakic Progress: Neurogenesis in adult primate neocortex: an evaluation of the evidence , 2002, Nature Reviews Neuroscience.

[76]  Jörg Fiedler,et al.  BMP‐2, BMP‐4, and PDGF‐bb stimulate chemotactic migration of primary human mesenchymal progenitor cells , 2002, Journal of cellular biochemistry.

[77]  R. Hebbel,et al.  Origins of circulating endothelial cells and endothelial outgrowth from blood. , 2000, The Journal of clinical investigation.

[78]  S. Rafii,et al.  Isolation and characterization of human bone marrow microvascular endothelial cells: hematopoietic progenitor cell adhesion. , 1994, Blood.

[79]  A. Frankfurter,et al.  The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis. , 1990, Cell motility and the cytoskeleton.