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. Author manuscript; available in PMC: 2019 Nov 1.
Published in final edited form as: Kidney Int. 2018 Sep 4;94(5):951–963. doi: 10.1016/j.kint.2018.06.010

Figure 3|. Adoptively-transferred Rictor−/− DC promote acute kidney injury.

Figure 3|

Bone marrow-derived CD11c+ DC from WT or Rictor−/− mice were adoptively transferred (5 × 106) intravenously into C57BL/6 mice 24 hr before bilateral renal IRI. After 24 h reperfusion, serum and kidneys were harvested and results compared to sham-operated mice and C57BL/6 mice not injected with cells. (a) Serum creatinine and blood urea nitrogen (BUN) levels from all mice. (b) Representative appearances and (c) semi-quantitative analysis of hematoxylin and eosin-stained kidney sections from sham-operated and post-IRI mice. Scale bars in (b) represent 50 m. Data shown are means +1SD; n=5–9 mice per group. *P < 0.05.