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dc.contributor.authorLindgren, D
dc.contributor.authorBoström, A
dc.contributor.authorNilsson, K
dc.contributor.authorHansson, J
dc.contributor.authorSjölund, J
dc.contributor.authorMöller, C
dc.contributor.authorJirström, K
dc.contributor.authorNilsson, E
dc.contributor.authorLandberg, Göran
dc.contributor.authorAxelson, H
dc.contributor.authorJohansson, M
dc.date.accessioned2011-11-25T16:29:31Z
dc.date.available2011-11-25T16:29:31Z
dc.date.issued2011-02
dc.identifier.citationIsolation and characterization of progenitor-like cells from human renal proximal tubules. 2011, 178 (2):828-37 Am J Patholen
dc.identifier.issn1525-2191
dc.identifier.pmid21281815
dc.identifier.doi10.1016/j.ajpath.2010.10.026
dc.identifier.urihttp://hdl.handle.net/10541/190855
dc.description.abstractThe tubules of the kidney display a remarkable capacity for self-renewal on damage. Whether this regeneration is mediated by dedifferentiating surviving cells or, as recently suggested, by stem cells has not been unequivocally settled. Herein, we demonstrate that aldehyde dehydrogenase (ALDH) activity may be used for isolation of cells with progenitor characteristics from adult human renal cortical tissue. Gene expression profiling of the isolated ALDH(high) and ALDH(low) cell fractions followed by immunohistochemical interrogation of renal tissues enabled us to delineate a tentative progenitor cell population scattered through the proximal tubules (PTs). These cells expressed CD24 and CD133, previously described markers for renal progenitors of Bowman's capsule. Furthermore, we show that the PT cells, and the glomerular progenitors, are positive for KRT7, KRT19, BCL2, and vimentin. In addition, tubular epithelium regenerating on acute tubular necrosis displayed long stretches of CD133(+)/VIM(+) cells, further substantiating that these cells may represent a progenitor cell population. Furthermore, a potential association of these progenitor cells with papillary renal cell carcinoma was discovered. Taken together, our data demonstrate the presence of a previously unappreciated subset of the PT cells that may be endowed with a more robust phenotype, allowing increased resistance to acute renal injury, enabling rapid repopulation of the tubules.
dc.language.isoenen
dc.subject.meshAdult
dc.subject.meshAldehyde Dehydrogenase
dc.subject.meshAntigens, CD
dc.subject.meshAntigens, CD24
dc.subject.meshCell Separation
dc.subject.meshFlow Cytometry
dc.subject.meshGene Expression Profiling
dc.subject.meshGlycoproteins
dc.subject.meshHumans
dc.subject.meshImmunohistochemistry
dc.subject.meshKidney Neoplasms
dc.subject.meshKidney Tubules, Proximal
dc.subject.meshPeptides
dc.subject.meshRegeneration
dc.subject.meshStem Cells
dc.subject.meshTranscription, Genetic
dc.subject.meshVimentin
dc.titleIsolation and characterization of progenitor-like cells from human renal proximal tubules.en
dc.typeArticleen
dc.contributor.departmentCenter for Molecular Pathology, Department of Laboratory Medicine, Lund University, SUS Malmö, Malmö, Sweden.en
dc.identifier.journalAmerican Journal of Pathologyen
html.description.abstractThe tubules of the kidney display a remarkable capacity for self-renewal on damage. Whether this regeneration is mediated by dedifferentiating surviving cells or, as recently suggested, by stem cells has not been unequivocally settled. Herein, we demonstrate that aldehyde dehydrogenase (ALDH) activity may be used for isolation of cells with progenitor characteristics from adult human renal cortical tissue. Gene expression profiling of the isolated ALDH(high) and ALDH(low) cell fractions followed by immunohistochemical interrogation of renal tissues enabled us to delineate a tentative progenitor cell population scattered through the proximal tubules (PTs). These cells expressed CD24 and CD133, previously described markers for renal progenitors of Bowman's capsule. Furthermore, we show that the PT cells, and the glomerular progenitors, are positive for KRT7, KRT19, BCL2, and vimentin. In addition, tubular epithelium regenerating on acute tubular necrosis displayed long stretches of CD133(+)/VIM(+) cells, further substantiating that these cells may represent a progenitor cell population. Furthermore, a potential association of these progenitor cells with papillary renal cell carcinoma was discovered. Taken together, our data demonstrate the presence of a previously unappreciated subset of the PT cells that may be endowed with a more robust phenotype, allowing increased resistance to acute renal injury, enabling rapid repopulation of the tubules.


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