Literature DB >> 28530000

Capillary endothelia from two ADPKD patients are polyploidy.

Sarmed H Kathem1,2, Wissam A AbouAlaiwi3, Xiaolin Zi2, Surya M Nauli1,2.   

Abstract

Bilateral renal cyst formation is the main feature of autosomal dominant polycystic kidney disease (ADPKD). We and other laboratories have previously shown that cyst-lining epithelia of kidneys from ADPKD patients are characterized by polyploidy. In this report, we show that endothelia from the renal capillary beds of two ADPKD patients are also polyploidy. Spectral karyotyping study further confirms our flow cytometry analyses. We suggest that polyploidy may be used as a potential cellular marker in ADPKD.

Entities:  

Year:  2016        PMID: 28530000      PMCID: PMC5436797     

Source DB:  PubMed          Journal:  Ann Clin Cytol Pathol


  13 in total

Review 1.  Autosomal dominant polycystic kidney disease: the last 3 years.

Authors:  Vicente E Torres; Peter C Harris
Journal:  Kidney Int       Date:  2009-05-20       Impact factor: 10.612

2.  Endothelial cells from humans and mice with polycystic kidney disease are characterized by polyploidy and chromosome segregation defects through survivin down-regulation.

Authors:  Wissam A AbouAlaiwi; Shobha Ratnam; Robert L Booth; Jagesh V Shah; Surya M Nauli
Journal:  Hum Mol Genet       Date:  2010-11-01       Impact factor: 6.150

3.  Intraflagellar transport protein 27 is a small G protein involved in cell-cycle control.

Authors:  Hongmin Qin; Zhaohui Wang; Dennis Diener; Joel Rosenbaum
Journal:  Curr Biol       Date:  2007-02-06       Impact factor: 10.834

4.  L-type calcium channel modulates cystic kidney phenotype.

Authors:  Xingjian Jin; Brian S Muntean; Munaf S Aal-Aaboda; Qiming Duan; Jing Zhou; Surya M Nauli
Journal:  Biochim Biophys Acta       Date:  2014-06-09

5.  Spectral karyotyping to study chromosome abnormalities in humans and mice with polycystic kidney disease.

Authors:  Wissam A AbouAlaiwi; Ingrid Rodriguez; Surya M Nauli
Journal:  J Vis Exp       Date:  2012-02-03       Impact factor: 1.355

6.  Loss of polycystin-1 causes centrosome amplification and genomic instability.

Authors:  Lorenzo Battini; Salvador Macip; Elena Fedorova; Steven Dikman; Stefan Somlo; Cristina Montagna; G Luca Gusella
Journal:  Hum Mol Genet       Date:  2008-06-19       Impact factor: 6.150

7.  Ciliary polycystin-2 is a mechanosensitive calcium channel involved in nitric oxide signaling cascades.

Authors:  Wissam A AbouAlaiwi; Maki Takahashi; Blair R Mell; Thomas J Jones; Shobha Ratnam; Robert J Kolb; Surya M Nauli
Journal:  Circ Res       Date:  2009-03-05       Impact factor: 17.367

8.  Centrosome overduplication and mitotic instability in PKD2 transgenic lines.

Authors:  Stéphane Burtey; Marta Riera; Emilie Ribe; Petra Pennenkamp; Roselyne Rance; Judith Luciani; Bernd Dworniczak; Marie Geneviève Mattei; Michel Fontés
Journal:  Cell Biol Int       Date:  2008-08-06       Impact factor: 3.612

Review 9.  Cardiovascular complications in autosomal dominant polycystic kidney disease.

Authors:  Tevfik Ecder
Journal:  Curr Hypertens Rev       Date:  2013-02

10.  Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease.

Authors:  Julie A Jonassen; Jovenal San Agustin; John A Follit; Gregory J Pazour
Journal:  J Cell Biol       Date:  2008-11-03       Impact factor: 10.539

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  1 in total

Review 1.  Epithelial proliferation and cell cycle dysregulation in kidney injury and disease.

Authors:  Kyung Lee; G Luca Gusella; John Cijiang He
Journal:  Kidney Int       Date:  2021-04-06       Impact factor: 18.998

  1 in total

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