Literature DB >> 21092402

Schwann cell coculture improves the therapeutic effect of bone marrow stromal cells on recovery in spinal cord-injured mice.

Xiaoyun Xu1, Nicole Geremia, Feng Bao, Anna Pniak, Melissa Rossoni, Arthur Brown.   

Abstract

Studies of bone marrow stromal cells (MSCs) transplanted into the spinal cord-injured rat give mixed results: some groups report improved locomotor recovery while others only demonstrate improved histological appearance of the lesion. These studies show no clear correlation between neurological improvements and MSC survival. We examined whether MSC survival in the injured spinal cord could be enhanced by closely matching donor and recipient mice for genetic background and marker gene expression and whether exposure of MSCs to a neural environment (Schwann cells) prior to transplantation would improve their survival or therapeutic effects. Mice underwent a clip compression spinal cord injury at the fourth thoracic level and cell transplantation 7 days later. Despite genetic matching of donors and recipients, MSC survival in the injured spinal cord was very poor (∼1%). However, we noted improved locomotor recovery accompanied by improved histopathological appearance of the lesion in mice receiving MSC grafts. These mice had more white and gray matter sparing, laminin expression, Schwann cell infiltration, and preservation of neurofilament and 5-HT-positive fibers at and below the lesion. There was also decreased collagen and chondroitin sulphate proteoglycan deposition in the scar and macrophage activation in mice that received the MSC grafts. The Schwann cell cocultured MSCs had greater effects than untreated MSCs on all these indices of recovery. Analyses of chemokine and cytokine expression revealed that MSC/Schwann cell cocultures produced far less MCP-1 and IL-6 than MSCs or Schwann cells cultured alone. Thus, transplanted MSCs may improve recovery in spinal cord-injured mice through immunosuppressive effects that can be enhanced by a Schwann cell coculturing step. These results indicate that the temporary presence of MSCs in the injured cord is sufficient to alter the cascade of pathological events that normally occurs after spinal cord injury, generating a microenvironment that favors improved recovery.

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Year:  2010        PMID: 21092402      PMCID: PMC4853195          DOI: 10.3727/096368910X544906

Source DB:  PubMed          Journal:  Cell Transplant        ISSN: 0963-6897            Impact factor:   4.064


  59 in total

1.  Marrow stromal cells form guiding strands in the injured spinal cord and promote recovery.

Authors:  C P Hofstetter; E J Schwarz; D Hess; J Widenfalk; A El Manira; Darwin J Prockop; L Olson
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2.  Bone marrow stromal cells enhance differentiation of cocultured neurosphere cells and promote regeneration of injured spinal cord.

Authors:  Sufan Wu; Yoshihisa Suzuki; Yoko Ejiri; Toru Noda; Hongliang Bai; Masaaki Kitada; Kazuya Kataoka; Masayoshi Ohta; Hirotomi Chou; Chizuka Ide
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3.  The recovery of 5-HT immunoreactivity in lumbosacral spinal cord and locomotor function after thoracic hemisection.

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Journal:  Exp Neurol       Date:  1996-06       Impact factor: 5.330

4.  Astroglial permissivity for neuritic outgrowth in neuron-astrocyte cocultures depends on regulation of laminin bioavailability.

Authors:  Silvia Costa; Thierry Planchenault; Cecile Charriere-Bertrand; Yann Mouchel; Christiane Fages; Sharon Juliano; Thierry Lefrançois; Georgia Barlovatz-Meimon; Marcienne Tardy
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Review 6.  A systematic review of cellular transplantation therapies for spinal cord injury.

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Review 4.  Adult bone marrow: which stem cells for cellular therapy protocols in neurodegenerative disorders?

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Journal:  Cell Transplant       Date:  2018-02       Impact factor: 4.064

6.  Polypyrrole/polylactic acid nanofibrous scaffold cotransplanted with bone marrow stromal cells promotes the functional recovery of spinal cord injury in rats.

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7.  Microglia-derived TNFα induces apoptosis in neural precursor cells via transcriptional activation of the Bcl-2 family member Puma.

Authors:  J Guadagno; X Xu; M Karajgikar; A Brown; S P Cregan
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8.  Rat Nasal Respiratory Mucosa-Derived Ectomesenchymal Stem Cells Differentiate into Schwann-Like Cells Promoting the Differentiation of PC12 Cells and Forming Myelin In Vitro.

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  8 in total

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