Human cadaver multipotent stromal/stem cells isolated from arteries stored in liquid nitrogen for 5 years

Stem Cell Res Ther. 2014 Jan 15;5(1):8. doi: 10.1186/scrt397.

Abstract

Introduction: Regenerative medicine challenges researchers to find noncontroversial, safe and abundant stem cell sources. In this context, harvesting from asystolic donors could represent an innovative and unlimited reservoir of different stem cells. In this study, cadaveric vascular tissues were established as an alternative source of human cadaver mesenchymal stromal/stem cells (hC-MSCs). We reported the successful cell isolation from postmortem arterial segments stored in a tissue-banking facility for at least 5 years.

Methods: After thawing, hC-MSCs were isolated with a high efficiency (12×10⁶) and characterized with flow cytometry, immunofluorescence, molecular and ultrastructural approaches.

Results: In early passages, hC-MSCs were clonogenic, highly proliferative and expressed mesenchymal (CD44, CD73, CD90, CD105, HLA-G), stemness (Stro-1, Oct-4, Notch-1), pericyte (CD146, PDGFR-β, NG2) and neuronal (Nestin) markers; hematopoietic and vascular markers were negative. These cells had colony and spheroid-forming abilities, multipotency for their potential to differentiate in multiple mesengenic lineages and immunosuppressive activity to counteract proliferation of phytohemagglutinin-stimulated blood mononuclear cells.

Conclusions: The efficient procurement of stem cells from cadaveric sources, as postmortem vascular tissues, demonstrates that such cells can survive to prolonged ischemic insult, anoxia, freezing and dehydration injuries, thus paving the way for a scientific revolution where cadaver stromal/stem cells could effectively treat patients demanding cell therapies.

MeSH terms

  • 5'-Nucleotidase / genetics
  • 5'-Nucleotidase / metabolism
  • Antigens / genetics
  • Antigens / metabolism
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Antigens, Surface / genetics
  • Antigens, Surface / metabolism
  • Arteries / cytology*
  • Arteries / drug effects
  • Cadaver
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Cryopreservation*
  • Endoglin
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / metabolism
  • HLA-G Antigens / genetics
  • HLA-G Antigens / metabolism
  • Humans
  • Hyaluronan Receptors / genetics
  • Hyaluronan Receptors / metabolism
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Mesenchymal Stem Cells / physiology
  • Nestin / genetics
  • Nestin / metabolism
  • Nitrogen / pharmacology
  • Octamer Transcription Factor-3 / genetics
  • Octamer Transcription Factor-3 / metabolism
  • Proteoglycans / genetics
  • Proteoglycans / metabolism
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism
  • Receptor, Platelet-Derived Growth Factor beta / genetics
  • Receptor, Platelet-Derived Growth Factor beta / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Stem Cell Research
  • Thy-1 Antigens / genetics
  • Thy-1 Antigens / metabolism
  • Tissue and Organ Harvesting / methods

Substances

  • Antigens
  • Antigens, CD
  • Antigens, Surface
  • CD44 protein, human
  • ENG protein, human
  • Endoglin
  • GPI-Linked Proteins
  • HLA-G Antigens
  • Hyaluronan Receptors
  • NOTCH1 protein, human
  • Nestin
  • Octamer Transcription Factor-3
  • POU5F1 protein, human
  • Proteoglycans
  • Receptor, Notch1
  • Receptors, Cell Surface
  • STRO-1 antigen, human
  • Thy-1 Antigens
  • chondroitin sulfate proteoglycan 4
  • Receptor, Platelet-Derived Growth Factor beta
  • 5'-Nucleotidase
  • NT5E protein, human
  • Nitrogen