Perirenal Adipose Tissue Displays an Age-Dependent Inflammatory Signature Associated With Early Graft Dysfunction of Marginal Kidney Transplants

Front Immunol. 2020 Mar 17:11:445. doi: 10.3389/fimmu.2020.00445. eCollection 2020.

Abstract

Background: Better understanding of the contribution of donor aging and comorbidity factors of expanded criteria donors (ECD) to the clinical outcome of a transplant is a challenge in kidney transplantation. We investigated whether the features of donor-derived stromal vascular fraction of perirenal adipose tissue (PRAT-SVF) could be indicative of the deleterious impact of the ECD microenvironment on a renal transplant. Methods: A comparative analysis of cellular components, transcriptomic and vasculogenic profiles was performed in PRAT-SVF obtained from 22 optimal donors and 31 ECD deceased donors. We then investigated whether these parameters could be associated with donor aging and early allograft dysfunction. Results: When compared with the PRAT-SVF of non-ECD donors, ECD PRAT-SVF displayed a lower proportion of stromal cells, a higher proportion of inflammatory NK cells. The global RNA sequencing approach indicated a differential molecular signature in the PRAT-SVF of ECD donors characterized by the over-expression of CXCL1 and IL1-β inflammatory transcripts. The vasculogenic activity of PRAT-SVF was highly variable but was not significantly affected in marginal donors. Periorgan recruitment of monocytes/macrophages and NK cells in PRAT-SVF was associated with donor aging. The presence of NK cell infiltrates was associated with lower PRAT-SVF angiogenic activity and with early allograft dysfunction evaluated on day 7 and at 1 month post-transplant. Conclusions: Our results indicate that human NK cell subsets are differentially recruited in the periorgan environment of aging kidney transplants. We provide novel evidence that PRAT-SVF represents a non-invasive and timely source of donor material with potential value to assess inflammatory features that impact organ quality and function.

Keywords: endothelial inflammation; kidney allograft dysfunction; kidney transplantation; marginal kidney donors; natural killer cells; perirenal adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / physiology*
  • Adult
  • Aged
  • Aging
  • Cell Movement
  • Chemokine CXCL1 / genetics
  • Chemokine CXCL1 / metabolism
  • Female
  • Humans
  • Inflammation / immunology*
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Kidney / immunology*
  • Kidney Transplantation*
  • Killer Cells, Natural / immunology*
  • Macrophages / immunology*
  • Male
  • Middle Aged
  • Neovascularization, Pathologic
  • Primary Graft Dysfunction / immunology*
  • Prospective Studies
  • Tissue Donors
  • Transcriptome
  • Transplants

Substances

  • Chemokine CXCL1
  • Interleukin-1beta