Cell Transplantation (Jan 2008)

Amelioration of Cisplatin-Induced Acute Renal Injury by Renal Progenitor-Like Cells Derived from the Adult Rat Kidney

  • Masaru Kinomura,
  • Shinji Kitamura,
  • Katsuyuki Tanabe,
  • Kunihiro Ichinose,
  • Kumiko Hirokoshi,
  • Yuki Takazawa,
  • Hiroyuki Kitayama,
  • Tatsuyo Nasu,
  • Hitoshi Sugiyama,
  • Yasushi Yamasaki,
  • Takeshi Sugaya,
  • Yohei Maeshima DR.,
  • Hirofumi Makino

DOI
https://doi.org/10.3727/000000008783907008
Journal volume & issue
Vol. 17

Abstract

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The replacement of a necrotic tubular epithelium with functional tubular epithelial cells is required for recovery from acute renal failure (ARF). A rat renal progenitor-like (rKS56) cell line was recently established derived from the S3 segment of renal proximal tubules. The therapeutic efficacy of rKS56 cells was examined in a rat model of cisplatin-induced ARF. rKS56-lacZ cells expressing β-galactosidase were injected into SD rats either at the subcapsule of the left kidney (rKS-SC) or via the left renal artery (rKS-IA) 2 days after the injection of cisplatin. Bluo-gal(+) rKS56-lacZ cells were observed in the subcapsule in the rKS-SC group on day 5, and were further increased in number on day 9, accompanied by partial distribution in the corticomedullary junction, but not in the rKS-IA group. A portion of Bluo-gal(+) cells coexpressed Ki-67, aquaporin-1, hepatocyte growth factor (HGF), and c-Met. rKS-SC treatment significantly improved the tubular injury scores, ameliorated tubular cell apoptosis, and induced cell proliferation. The renal function also significantly improved in the rKS-SC group on day 5. These results demonstrate that locally implanted rKS56 cells could differentiate into tubular epithelial cells, thereby accelerating the recovery from tubular injury, most likely by producing tubular trophic factors. These results suggest the therapeutic potential of this novel approach for patients with end-stage renal failure.