Literature DB >> 10484529

Expression of NCAM recapitulates tubulogenic development in kidneys recovering from acute ischemia.

M Abbate1, D Brown, J V Bonventre.   

Abstract

Recovery of the kidney from acute renal failure relies on a sequence of events including epithelial cell dedifferentiation and proliferation followed by differentiation and restoration of the functional integrity of the nephron. The factors responsible for, and the significance of, reversion to a less differentiated cell phenotype and its relationship to the proliferative response after ischemia are poorly understood. In an attempt to identify adhesion molecules that may be influential in the recovery process, the expression of neural cell adhesion molecule (NCAM) and markers of epithelial differentiation and proliferation were analyzed at various times after an ischemic insult. In maturing nephrons, NCAM is detectable by immunohistochemistry in renal vesicles, S-shaped bodies, and early tubules. There is minimal cellular NCAM expression in normal tubules of the adult kidney. In contrast, in postischemic kidneys, NCAM expression is abundant in S3 proximal tubule cells 5 days after reperfusion. As in developing tubules, NCAM is concentrated in basal and lateral aspects of cells that have no apical gp330 or dipeptidyl peptidase IV detectable on their brush border. The expression of NCAM is preceded by disassembly of the brush border and proliferation of surviving S3 cells, which is most prominent at 2 days postischemia. NCAM expression persists in some flattened and dedifferentiated cells for up to 7 wk after ischemia. Thus proximal tubule epithelial cells of the postischemic kidney express NCAM in a pattern that recapitulates the expression of NCAM in the developing kidney. Such reversion of phenotype extends at least back to the early stages of renal vesicle formation, and this reversion may represent a critical step in the reestablishment of a normal tubule. NCAM-matrix interactions may mediate the motogenic and mitogenic responses of the dedifferentiated epithelium that are critical to reestablishment of a functional proximal tubule.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10484529     DOI: 10.1152/ajprenal.1999.277.3.F454

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  30 in total

1.  AMPK protects proximal tubular cells from stress-induced apoptosis by an ATP-independent mechanism: potential role of Akt activation.

Authors:  Wilfred Lieberthal; Leiqing Zhang; Vimal A Patel; Jerrold S Levine
Journal:  Am J Physiol Renal Physiol       Date:  2011-09-28

Review 2.  Therapeutic use of human renal progenitor cells for kidney regeneration.

Authors:  Benedetta Bussolati; Giovanni Camussi
Journal:  Nat Rev Nephrol       Date:  2015-08-04       Impact factor: 28.314

Review 3.  Stromal cells in tissue homeostasis: balancing regeneration and fibrosis.

Authors:  Ton J Rabelink; Melissa H Little
Journal:  Nat Rev Nephrol       Date:  2013-08-13       Impact factor: 28.314

Review 4.  Selecting the optimal cell for kidney regeneration: fetal, adult or reprogrammed stem cells.

Authors:  Orit Harari-Steinberg; Oren Pleniceanu; Benjamin Dekel
Journal:  Organogenesis       Date:  2011-04-01       Impact factor: 2.500

Review 5.  Cellular plasticity in kidney injury and repair.

Authors:  Monica Chang-Panesso; Benjamin D Humphreys
Journal:  Nat Rev Nephrol       Date:  2016-11-28       Impact factor: 28.314

6.  Gas1 expression in parietal cells of Bowman's capsule in experimental diabetic nephropathy.

Authors:  Brenda I Luna-Antonio; Rafael Rodriguez-Muñoz; Carmen Namorado-Tonix; Paula Vergara; Jose Segovia; Jose L Reyes
Journal:  Histochem Cell Biol       Date:  2017-03-18       Impact factor: 4.304

7.  In vivo maturation of functional renal organoids formed from embryonic cell suspensions.

Authors:  Christodoulos Xinaris; Valentina Benedetti; Paola Rizzo; Mauro Abbate; Daniela Corna; Nadia Azzollini; Sara Conti; Mathieu Unbekandt; Jamie A Davies; Marina Morigi; Ariela Benigni; Giuseppe Remuzzi
Journal:  J Am Soc Nephrol       Date:  2012-10-18       Impact factor: 10.121

Review 8.  Renal lineage cells as a source for renal regeneration.

Authors:  Oren Pleniceanu; Dorit Omer; Orit Harari-Steinberg; Benjamin Dekel
Journal:  Pediatr Res       Date:  2017-11-15       Impact factor: 3.756

9.  Expression of nestin, vimentin, and NCAM by renal interstitial cells after ischemic tubular injury.

Authors:  David Vansthertem; Annabel Gossiaux; Anne-Emilie Declèves; Nathalie Caron; Denis Nonclercq; Alexandre Legrand; Gérard Toubeau
Journal:  J Biomed Biotechnol       Date:  2010-06-14

10.  Ischemia induces early expression of a new transcription factor (6A3-5) in kidney vascular smooth muscle cells: studies in rat and human renal pathology.

Authors:  Gwenaële Garin; Chérif Badid; Brigitte McGregor; Madeleine Vincent; Sylviane Guerret; Kazem Zibara; Adam Hurlstone; Maurice Laville; John L McGregor
Journal:  Am J Pathol       Date:  2003-12       Impact factor: 4.307

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.