R2: Identification of renal potential progenitor/stem cells that participate in the renal regeneration processes of kidney allograft fibrosis

Aim:  Many strategies are explored to ameliorate kidney allograft tubular atrophy and interstitial fibrosis (TA/IF), but little progress has been achieved. The latest evidence suggested that CD133+ cell in kidney represent a potential multipotent adult resident stem cell population that may contribu...

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Veröffentlicht in:Nephrology (Carlton, Vic.) Vic.), 2008-09, Vol.13 (6), p.500-507
Hauptverfasser: BAO, JI, TU, ZHIDAN, SUN, HUAIQIANG, LUO, GUANGHENG, YANG, LI, SONG, JUN, QIN, MINGXIA, SHI, YUJUN, BU, HONG, LI, YOUPING
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Sprache:eng
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Zusammenfassung:Aim:  Many strategies are explored to ameliorate kidney allograft tubular atrophy and interstitial fibrosis (TA/IF), but little progress has been achieved. The latest evidence suggested that CD133+ cell in kidney represent a potential multipotent adult resident stem cell population that may contribute to the renal injury repair. Here we investigate whether the CD133+ cells exist in transplanted renal and exert a growth and self‐repair procedure in TA/IF. Methods:  Allografts from rat kidney transplant models were harvested at 4 weeks, 8 weeks and 12 weeks post transplantation. We performed immunohistochemistry to detect the CD133+ cells and immunofluorescence to detect the co‐expression of CD133 or Pax‐2 with Ki‐67. We furthermore analysed the E‐cadherin using serial sections. Results:  CD133+ cells were seldom seen in control kidney, but distributed sporadically in the cortex parenchyma along with the deterioration of TA/IF. The number of CD133+ cell increased after 4 weeks and reached the peak at 8 weeks, then decreased at 12 weeks. From 8 weeks, some new tubules expressing E‐cadherin were constructed with CD133+ cells. Almost all the CD133+ cells were Ki‐67‐positive, but not all the Ki‐67+ cells expressed CD133. The rest Ki‐67+ cells almost expressed Pax‐2. Conclusion:  Our study reveals that when majority of the tubules are damaged, a self‐repair mechanism is evoked by potential adult stem cells to compensate the renal function. Thus, potential adult resident stem cells offer a new avenue for autologous cell therapies in TA/IF.
ISSN:1320-5358
1440-1797
DOI:10.1111/j.1440-1797.2008.00939.x