4.5 Article

Aberrant activation of the complement system in renal grafts is mediated by cold storage

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
Volume 320, Issue 6, Pages F1174-F1190

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajprenal.00670.2020

Keywords

cold storage; complement system; transplantation

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases [R01DK123264]
  2. American Heart Association [16SDG276000026, 19TPA34850057]
  3. Barton Pilot award
  4. Medical Research Endowment award
  5. Marion B. Lyon New Scientist Development award

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This study revealed that cold storage leads to aberrant activation of complement components in renal grafts following transplantation, with increased levels of C3 and C5b-9. Additionally, cold storage induced local C3 biogenesis in renal proximal cells/tubules, and TNF-alpha was found to promote C3 biogenesis and activation in renal proximal tubular cells.
Aberrant complement activation leads to tissue damage during kidney transplantation, and it is recognized as an important target for therapeutic intervention. However, it is not clear whether cold storage (CS) triggers the complement pathway in transplanted kidneys. The goal of the present study was to determine the impact of CS on complement activation in renal transplants. Male Lewis and Fischer rats were used, and donor rat kidneys were exposed to 4 h or 18 h of CS followed by transplantation (CS thorn transplant). To study CS-induced effects, a group with no CS was included in which the kidney was removed and transplanted back to the same rat [autotransplantation (ATx)]. Complement proteins (C3 and C5b-9) were evaluated with Western blot analysis (reducing and nonreducing conditions) and immunostaining. Western blot analysis of renal extracts or serum indicated that the levels of C3 and C5b-9 increased after CS thorn transplant compared with ATx. Quite strikingly, intracellular C3 was profoundly elevated within renal tubules after CS thorn transplant but was absent in sham or ATx groups, which showed only extratubular C3. Similarly, C5b-9 immunofluorescence staining of renal sections showed an increase in C5b-9 deposits in kidneys after CS thorn transplant. Real-time PCR (SYBR green) showed increased expression of CD11b and CD11c, components of complement receptors 3 and 4, respectively, as well as inflammatory markers such as TNF-alpha. In addition, recombinant TNF-alpha significantly increased C3 levels in renal cells. Collectively, these results demonstrate that CS mediates aberrant activation of the complement system in renal grafts following transplantation. NEW & NOTEWORTHY This study highlights cold storage-mediated aberrant activation of complement components in renal allografts following transplantation. Specifically, the results demonstrate, for the first time, that cold storage functions in exacerbation of C5b-9, a terminal cytolytic membrane attack complex, in renal grafts following transplantation. In addition, the results indicated that cold storage induces local C3 biogenesis in renal proximal cells/tubules and that TNF-alpha promotes C3 biogenesis and activation in renal proximal tubular cells.

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