Literature DB >> 25847030

Microvesicles Derived From Human Mesenchymal Stem Cells Restore Alveolar Fluid Clearance in Human Lungs Rejected for Transplantation.

S Gennai1, A Monsel2, Q Hao3, J Park3, M A Matthay3,4, J W Lee3.   

Abstract

The need to increase the donor pool for lung transplantation is a major public health issue. We previously found that administration of mesenchymal stem cells "rehabilitated" marginal donor lungs rejected for transplantation using ex vivo lung perfusion. However, the use of stem cells has some inherent limitation such as the potential for tumor formation. In the current study, we hypothesized that microvesicles, small anuclear membrane fragments constitutively released from mesenchymal stem cells, may be a good alternative to using stem cells. Using our well established ex vivo lung perfusion model, microvesicles derived from human mesenchymal stem cells increased alveolar fluid clearance (i.e. ability to absorb pulmonary edema fluid) in a dose-dependent manner, decreased lung weight gain following perfusion and ventilation, and improved airway and hemodynamic parameters compared to perfusion alone. Microvesicles derived from normal human lung fibroblasts as a control had no effect. Co-administration of microvesicles with anti-CD44 antibody attenuated these effects, suggesting a key role of the CD44 receptor in the internalization of the microvesicles into the injured host cell and its effect. In summary, microvesicles derived from human mesenchymal stem cells were as effective as the parent mesenchymal stem cells in rehabilitating marginal donor human lungs. © Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons.

Entities:  

Keywords:  lung failure/injury; stem cells; tissue injury and repair

Mesh:

Year:  2015        PMID: 25847030      PMCID: PMC4792255          DOI: 10.1111/ajt.13271

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  33 in total

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Authors:  Marcelo Cypel; Shaf Keshavjee
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3.  Mesenchymal stem cell-derived microvesicles protect against acute tubular injury.

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4.  Allogeneic human mesenchymal stem cells for treatment of E. coli endotoxin-induced acute lung injury in the ex vivo perfused human lung.

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5.  Normothermic ex vivo lung perfusion in clinical lung transplantation.

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7.  Allogeneic human mesenchymal stem cells restore epithelial protein permeability in cultured human alveolar type II cells by secretion of angiopoietin-1.

Authors:  Xiaohui Fang; Arne P Neyrinck; Michael A Matthay; Jae W Lee
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10.  Angiopoietin-1 alters microvascular permeability coefficients in vivo via modification of endothelial glycocalyx.

Authors:  Andrew H J Salmon; Christopher R Neal; Leslie M Sage; Catherine A Glass; Steven J Harper; David O Bates
Journal:  Cardiovasc Res       Date:  2009-03-18       Impact factor: 10.787

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  60 in total

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2.  Extracellular Vesicle Transfer from Mesenchymal Stromal Cells Modulates Macrophage Function in Acute Lung Injury. Basic Science and Clinical Implications.

Authors:  Michael A Matthay
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Review 3.  Lung transplantation, ex-vivo reconditioning and regeneration: state of the art and perspectives.

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4.  Inhalational delivery of induced pluripotent stem cell secretome improves postpneumonectomy lung structure and function.

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Review 5.  Extracellular Vesicles: A New Frontier for Research in Acute Respiratory Distress Syndrome.

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6.  Mesenchymal stem cell-derived extracellular vesicles attenuate pulmonary vascular permeability and lung injury induced by hemorrhagic shock and trauma.

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Review 7.  Mesenchymal Stem Cells on Horizon: A New Arsenal of Therapeutic Agents.

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8.  Extracellular Vesicle Biology in the Pathogenesis of Lung Disease.

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9.  Therapeutic effects of human mesenchymal stem cell microvesicles in an ex vivo perfused human lung injured with severe E. coli pneumonia.

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10.  Mesenchymal Stromal Cell Exosomes Ameliorate Experimental Bronchopulmonary Dysplasia and Restore Lung Function through Macrophage Immunomodulation.

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