The kidney papilla contains a population of cells with several characteristics of adult stem cells, including the retention of proliferation markers during long chase periods (i.e., they are label-retaining cells [LRCs]). To determine whether the papillary LRCs generate new cells in the normal adult kidney, we examined cell proliferation throughout the kidney and found that the upper papilla is a site of enhanced cell cycling. Using genetically modified mice that conditionally expressed green fluorescence protein fused to histone 2B, we observed that the LRCs of the papilla proliferated only in its upper part, where they associate with "chains" of cycling cells. The papillary LRCs decreased in number with age, suggesting that the cells migrated to the upper papilla before entering the cell cycle. To test this directly, we marked papillary cells with vital dyes in vivo and found that some cells in the kidney papilla, including LRCs, migrated toward other parts of the kidney. Acute kidney injury enhanced both cell migration and proliferation. These results suggest that during normal homeostasis, LRCs of the kidney papilla (or their immediate progeny) migrate to the upper papilla and form a compartment of rapidly proliferating cells, which may play a role in repair after ischemic injury. Adult stem cells contribute to organ repair after injury 1-5 ; however, their contribution to normal tissue homeostasis by the generation of a continuous supply of new cells has not been readily apparent, except in tissues with relatively simple architecture and high rate of cell turnover, such as the skin and the intestinal epithelia. 1,6 In addition, recent studies have shown that in some organs, precursor cells responsible for homeostatic cell turnover are different from those responsible for cell replacement after injury. For example, stem cells in the bulge of the hair follicle contribute to wound repair, 5 but normal cell turnover of the epidermis is maintained by a distinct progenitor population located in the interfollicular epidermis. 7 In the olfactory neuroepithelium, a site of continuous neurogenesis under normal conditions in the adult, new neurons are generated by the globose basal cells that reside in the basal germinal zone of the pseudostratified olfactory neuroepithelium; however, after extensive tissue damage, another population of cells (horizontal basal cells) starts proliferating and generates several cell types. 8 Finally,  cells of the pancreas are maintained by proliferation of terminally differentiated  cells, 9,10 but in injured pancreas, multipotent progenitor cells can give rise to  cells. 11 The normal adult kidney has a very low rate of cell turnover, 12 but it is capable of responding quickly to injury by generating new cells to replace