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Am J Physiol Renal Physiol 297: F809-F815, 2009. First published June 17, 2009; doi:10.1152/ajprenal.90650.2008
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The long-term label retaining population of the renal papilla arises through divergent regional growth of the kidney

Derek C. Adams and Leif Oxburgh

Center for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine

Submitted 30 October 2008 ; accepted in final form 12 June 2009

Long-term pulse chase experiments previously identified a sizable population of BrdU-retaining cells within the renal papilla. The origin of these cells has been unclear, and in this work we test the hypothesis that they become quiescent early during the course of kidney development and organ growth. Indeed, we find that BrdU-retaining cells of the papilla can be labeled only by pulsing with BrdU from embryonic (E) day 11.25 to postnatal (P) day 7, the approximate period of kidney development in the mouse. BrdU signal in the cortex and outer medulla is rapidly diluted by cellular proliferation during embryonic development and juvenile growth, whereas cells within the papilla differentiate and exit the cell cycle during organogenesis. Indeed, by E17.5, little or no active proliferation can be seen in the distal papilla, indicating maturation of this structure in a distal-to-proximal manner during organogenesis. We conclude that BrdU-retaining cells of the papilla represent a population of cells that quiesce during embryonic development and localize within a region of the kidney that matures early. We therefore propose that selective papillary retention of BrdU arises through a combination of regionalized slowing of, and exit from, the cell cycle within the papilla during the period of ongoing kidney development, and extensive proliferative growth of the juvenile kidney resulting in dilution of BrdU below the detection level in extra-papillary regions.

BrdU-retaining cells; renal stem cells; renal progenitor cells; kidney growth; kidney development



Address for reprint requests and other correspondence: L. Oxburgh, Center for Molecular Medicine, Maine Medical Center Research Institute, 81 Research Drive, Scarborough, ME 04074 (e-mail: oxburl{at}mmc.org)







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