Summary: The bladder urothelium functions as a urine-blood barrier and consists of basal, intermediate, and superficial cell populations. Reconstructive procedures such as augmentation cystoplasty and focal mucosal resection involve localized surgical damage to the bladder wall whereby focal segments of the urothelium and underlying submucosa are respectively removed or replaced and regeneration ensues. We demonstrate using lineage-tracing systems that urothelial regeneration following augmentation cystoplasty with acellular grafts exclusively depends on host keratin 5-expressing basal cells to repopulate all lineages of the de novo urothelium at implant sites. Conversely, repair of focal mucosal defects not only employs this mechanism, but in parallel host intermediate cell daughters expressing uroplakin 2 give rise to themselves and are also contributors to superficial cells in neotissues. These results highlight the diversity of urothelial regenerative responses to surgical injury and may lead to advancements in bladder tissue engineering approaches. : In this article, Mauney and colleagues show the source of urothelial progenitors utilized during bladder regeneration is dependent on the nature of injury. Fate-mapping experiments reveal that host basal and intermediate cell progeny differentially contribute to de novo urothelial formation in bladder augmentation and mucosal resection settings. These results highlight the diversity of urothelial regenerative responses to surgical injury. Keywords: bladder, tissue engineering, progenitor, urothelium