Marco Eijken

Infusing Mesenchymal Stromal Cells into Porcine Kidneys during Normothermic Machine Perfusion: Intact MSCs Can Be Traced and Localised to Glomeruli

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DOI

  • Merel Pool, Department of Surgery-Organ Donation and Transplantation, University Medical Center, 9713 GZ Groningen, The Netherlands. m.b.f.pool@umcg.nl.
  • ,
  • Tim Eertman, Department of Surgery-Organ Donation and Transplantation, University Medical Center, 9713 GZ Groningen, The Netherlands.
  • ,
  • Jesus Sierra Parraga
  • Nils 't Hart, Department of Pathology and Medical Biology, GRIAC, University of Groningen, University Medical Center Groningen, Groningen, NL - 9713 GZ, The Netherlands.
  • ,
  • Marieke Roemeling-van Rhijn, University of Groningen
  • ,
  • Marco Eijken
  • Bente Jespersen
  • Marlies Reinders, Leiden University
  • ,
  • Martin Hoogduijn, Department of Internal Medicine, Erasmus Medical Center, Rotterdam, 3015 GE, The Netherlands.
  • ,
  • Rutger Ploeg, Oxford Transplant Centre, University of Oxford, OX3 7LJ Oxford, UK.
  • ,
  • Henri Leuvenink, Department of Surgery-Organ Donation and Transplantation, University Medical Center, 9713 GZ Groningen, The Netherlands.
  • ,
  • Cyril Moers, Department of Surgery-Organ Donation and Transplantation, University Medical Center, 9713 GZ Groningen, The Netherlands.

Normothermic machine perfusion (NMP) of kidneys offers the opportunity to perform active interventions, such as the addition of mesenchymal stromal cells (MSCs), to an isolated organ prior to transplantation. The purpose of this study was to determine whether administering MSCs to kidneys during NMP is feasible, what the effect of NMP is on MSCs and whether intact MSCs are retained in the kidney and to which structures they home. Viable porcine kidneys were obtained from a slaughterhouse. Kidneys were machine perfused during 7 h at 37 °C. After 1 h of perfusion either 0, 105, 106 or 107 human adipose tissue derived MSCs were added. Additional ex vivo perfusions were conducted with fluorescent pre-labelled bone-marrow derived MSCs to assess localisation and survival of MSCs during NMP. After NMP, intact MSCs were detected by immunohistochemistry in the lumen of glomerular capillaries, but only in the 107 MSC group. The experiments with fluorescent pre-labelled MSCs showed that only a minority of glomeruli were positive for infused MSCs and most of these glomeruli contained multiple MSCs. Flow cytometry showed that the number of infused MSCs in the perfusion circuit steeply declined during NMP to approximately 10%. In conclusion, the number of circulating MSCs in the perfusate decreases rapidly in time and after NMP only a small portion of the MSCs are intact and these appear to be clustered in a minority of glomeruli.

OriginalsprogEngelsk
Artikelnummer3607
TidsskriftInternational Journal of Molecular Sciences
Vol/bind20
Nummer14
ISSN1661-6596
DOI
StatusUdgivet - jul. 2019

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