Publication

Dendritic cells facilitate accumulation of il-17t cells in the kidney following acute renal obstruction

Dong, Xiangyang
Bachman, Lori A.
Miller, Melinda N.
Nath, Karl A.
Griffin, Matthew D.
Citation
Dong, Xiangyang; Bachman, Lori A. Miller, Melinda N.; Nath, Karl A.; Griffin, Matthew D. (2008). Dendritic cells facilitate accumulation of il-17t cells in the kidney following acute renal obstruction. Kidney International 74 (10), 1294-1309
Abstract
Acute urinary obstruction causes interstitial inflammation with leukocyte accumulation and the secretion of soluble mediators. Here we show that unilateral ureteral ligation caused a progressive increase in renal F4/80(+) and F4/80(-) dendritic cells, monocytes, neutrophils and T-cells 24-72 h following obstruction. Depletion of dendritic cells by clodronate pretreatment showed these cells to be the most potent source of tumor necrosis factor and other pro-inflammatory mediators in the obstructed kidney. F4/80(+) dendritic cells and T-cells co-localized in the cortico-medullary junction and cortex of the obstructed kidney. Cytokine secretion patterns and surface phenotypes of T-cells from obstructed kidneys were found to include interferon-gamma-secreting CD4(+) and CD8(+) memory T-cells as well as interleukin 17 (IL-17)-secreting CD4(+) memory T-cells. Depletion of the intra-renal dendritic cells prior to ligation did not numerically reduce T-cells in obstructed kidneys but attenuated interferon-gamma and IL-17-competent T-cells. Our study shows that intra-renal dendritic cells are a previously unidentified early source of proinflammatory mediators after acute urinary obstruction and play a specific role in recruitment and activation of effector-memory T-cells including IL-17-secreting CD4(+) T-cells.
Funder
Publisher
Elsevier BV
Publisher DOI
10.1038/ki.2008.394
Rights
Attribution-NonCommercial-NoDerivs 3.0 Ireland