Literature DB >> 15100366

Hematopoietic stem cell mobilization-associated granulocytosis severely worsens acute renal failure.

Florian Tögel1, Jorge Isaac, Christof Westenfelder.   

Abstract

Acute renal failure (ARF), resulting from ischemic or toxic insults, remains a major health care problem because of its grave prognosis and the limited effectiveness of available treatment modalities. On the basis of the recent demonstration that hematopoietic stem cells can differentiate into renal cells and the authors' observation here that ARF results in a rise in peripheral CD34+ cells, the authors tested whether a further increase in circulating stem cell numbers, induced by their mobilization from the bone marrow, would improve renal function and outcome in mice with ischemic ARF. Unexpected, it was found that the boosting of peripheral stem cell numbers failed to exert any renoprotective effects but rather was associated both with greatly increased severity of renal failure and mortality. Because identical ischemic injury in neutropenic mice resulted in milder renal insufficiency and significantly reduced mortality, it was deduced that the adverse effects of pharmacologic stem cell mobilization are primarily mediated by the concomitant induction of marked granulocytosis. In this manner, high numbers of activated granulocytes seem to obscure the potential renoprotective and positive survival effects of pluripotent hematopoietic stem cells, mediated by both their injurious renal and systemic actions. The data strongly argue against the clinical use of granulocytosis-inducing hematopoietic stem cell mobilization protocols for the prevention or treatment of ischemic ARF. Additional caution with this regimen may be warranted in patients with underlying renal insufficiency and those who develop renal insufficiency while undergoing stem cell mobilization in preparation for an autologous bone marrow transplant.

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Year:  2004        PMID: 15100366     DOI: 10.1097/01.asn.0000123692.01237.0a

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  21 in total

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Journal:  Biochim Biophys Acta       Date:  2014-03-14

3.  Exploration of disease mechanism in acute kidney injury using a multiplex bead array assay: a nested case-control pilot study.

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Journal:  Biomarkers       Date:  2010-08       Impact factor: 2.658

4.  Intrarenal cells, not bone marrow-derived cells, are the major source for regeneration in postischemic kidney.

Authors:  Fangming Lin; Ashley Moran; Peter Igarashi
Journal:  J Clin Invest       Date:  2005-07       Impact factor: 14.808

5.  Hematopoietic stem cells derived from human umbilical cord ameliorate cisplatin-induced acute renal failure in rats.

Authors:  Rokaya H Shalaby; Laila A Rashed; Alaa E Ismaail; Naglaa K Madkour; Sherien H Elwakeel
Journal:  Am J Stem Cells       Date:  2014-09-05

Review 6.  Pathophysiology of acute kidney injury.

Authors:  David P Basile; Melissa D Anderson; Timothy A Sutton
Journal:  Compr Physiol       Date:  2012-04       Impact factor: 9.090

Review 7.  Renal repair: role of bone marrow stem cells.

Authors:  Fangming Lin
Journal:  Pediatr Nephrol       Date:  2008-06       Impact factor: 3.714

8.  The cellular origin and proliferative status of regenerating renal parenchyma after mercuric chloride damage and erythropoietin treatment.

Authors:  T-H Yen; M R Alison; H T Cook; R Jeffery; W R Otto; N A Wright; R Poulsom
Journal:  Cell Prolif       Date:  2007-04       Impact factor: 6.831

Review 9.  Review article: endothelial progenitor cells in renal disease.

Authors:  Michael S Goligorsky; Mei-Chuan Kuo; Daniel Patschan; Marianne C Verhaar
Journal:  Nephrology (Carlton)       Date:  2009-04       Impact factor: 2.506

Review 10.  Stem cells: potential and challenges for kidney repair.

Authors:  Marcela Herrera; Maria Mirotsou
Journal:  Am J Physiol Renal Physiol       Date:  2013-11-06
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