Literature DB >> 27798243

Does Renal Repair Recapitulate Kidney Development?

Melissa Helen Little1,2, Pamela Kairath3,2.   

Abstract

Over a decade ago, it was proposed that the regulation of tubular repair in the kidney might involve the recapitulation of developmental pathways. Although the kidney cannot generate new nephrons after birth, suggesting a low level of regenerative competence, the tubular epithelial cells of the nephrons can proliferate to repair the damage after AKI. However, the debate continues over whether this repair involves a persistent progenitor population or any mature epithelial cell remaining after injury. Recent reports have highlighted the expression of Sox9, a transcription factor critical for normal kidney development, during postnatal epithelial repair in the kidney. Indeed, the proliferative response of the epithelium involves expression of several pathways previously described as being involved in kidney development. In some instances, these pathways are also apparently involved in the maladaptive responses observed after repeated injury. Whether development and repair in the kidney are the same processes or we are misinterpreting the similar expression of genes under different circumstances remains unknown. Here, we review the evidence for this link, concluding that such parallels in expression may more correctly represent the use of the same pathways in a distinct context, likely triggered by similar stressors.
Copyright © 2016 by the American Society of Nephrology.

Entities:  

Keywords:  Maladaptive repair; acute tubular injury; ischemia-reperfusion; kidney development; transcriptional profiling; tubular repair

Mesh:

Year:  2016        PMID: 27798243      PMCID: PMC5198297          DOI: 10.1681/ASN.2016070748

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


  124 in total

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7.  Sox9-Positive Progenitor Cells Play a Key Role in Renal Tubule Epithelial Regeneration in Mice.

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Review 8.  Dedifferentiation and proliferation of surviving epithelial cells in acute renal failure.

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6.  Comparing development and regeneration in the submandibular gland highlights distinct mechanisms.

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9.  Adipose-derived mesenchymal stem cells employed exosomes to attenuate AKI-CKD transition through tubular epithelial cell dependent Sox9 activation.

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