Literature DB >> 24493869

PDGF and the progression of renal disease.

Peter Boor1, Tammo Ostendorf, Jürgen Floege.   

Abstract

Progressive renal diseases represent a global medical problem, in part because we currently lack effective treatment strategies. Inhibition of platelet-derived growth factors (PDGFs) might represent one such novel strategy. PDGFs are required for normal kidney development by the recruitment of mesenchymal cells to both glomeruli and the interstitium. PDGFs are expressed in renal mesenchymal cells and, upon injury, in epithelial and infiltrating cells. They exert autocrine and paracrine effects on PDGF receptor-bearing mesenchymal cells, i.e. mesangial cells, fibroblasts and vascular smooth-muscle cells, which are crucially involved in progressive renal diseases. Proliferation but also migration and activation of these mesenchymal cells are the major effects mediated by PDGFs. These actions predefine the major roles of PDGFs in renal pathology, particularly in mesangioproliferative glomerulonephritis and interstitial fibrosis. Whereas for the former, the role of PDGFs is very well described and established, the latter is increasingly better documented as well. An involvement of PDGFs in other renal diseases, e.g. acute kidney injury, vascular injury and hypertensive as well as diabetic nephropathy, is less well established or presently unknown. Nevertheless, PDGFs represent a promising therapeutic option for progressive renal diseases, especially those characterized by mesangial cell proliferation and interstitial fibrosis. Clinical studies are eagerly awaited, in particular, since several drugs inhibiting PDGF signalling are available for clinical testing.

Entities:  

Keywords:  chronic kidney disease; fibroblasts; fibrosis; mesangial cells; platelet-derived growth factors

Mesh:

Substances:

Year:  2014        PMID: 24493869     DOI: 10.1093/ndt/gft273

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN: 0931-0509            Impact factor:   5.992


  37 in total

1.  Platelets are relevant mediators of renal injury induced by primary endothelial lesions.

Authors:  Claudia Schwarzenberger; Jan Sradnick; Kenneth M Lerea; Michael S Goligorsky; Bernhard Nieswandt; Christian P M Hugo; Bernd Hohenstein
Journal:  Am J Physiol Renal Physiol       Date:  2015-04-01

2.  Tyrosines-740/751 of PDGFRβ contribute to the activation of Akt/Hif1α/TGFβ nexus to drive high glucose-induced glomerular mesangial cell hypertrophy.

Authors:  Falguni Das; Nandini Ghosh-Choudhury; Balakuntalam S Kasinath; Goutam Ghosh Choudhury
Journal:  Cell Signal       Date:  2017-09-23       Impact factor: 4.315

3.  PDGF receptor-β uses Akt/mTORC1 signaling node to promote high glucose-induced renal proximal tubular cell collagen I (α2) expression.

Authors:  Falguni Das; Nandini Ghosh-Choudhury; Balachandar Venkatesan; Balakuntalam S Kasinath; Goutam Ghosh Choudhury
Journal:  Am J Physiol Renal Physiol       Date:  2017-04-19

Review 4.  Targeting CTGF, EGF and PDGF pathways to prevent progression of kidney disease.

Authors:  Helena M Kok; Lucas L Falke; Roel Goldschmeding; Tri Q Nguyen
Journal:  Nat Rev Nephrol       Date:  2014-10-14       Impact factor: 28.314

5.  Resistant starch supplementation attenuates inflammation in hemodialysis patients: a pilot study.

Authors:  Bruna Regis de Paiva; Marta Esgalhado; Natália Alvarenga Borges; Julie Ann Kemp; Gutemberg Alves; Paulo Emílio Corrêa Leite; Renata Macedo; Ludmila F M F Cardozo; Jessyca Sousa de Brito; Denise Mafra
Journal:  Int Urol Nephrol       Date:  2020-02-01       Impact factor: 2.370

6.  Ascending Vasa Recta Are Angiopoietin/Tie2-Dependent Lymphatic-Like Vessels.

Authors:  Yael Kenig-Kozlovsky; Rizaldy P Scott; Tuncer Onay; Isabel Anna Carota; Benjamin R Thomson; Hyea Jin Gil; Veronica Ramirez; Shinji Yamaguchi; Christine E Tanna; Stefan Heinen; Christine Wu; Radu V Stan; Janet D Klein; Jeff M Sands; Guillermo Oliver; Susan E Quaggin
Journal:  J Am Soc Nephrol       Date:  2017-12-13       Impact factor: 10.121

7.  TGFβ acts through PDGFRβ to activate mTORC1 via the Akt/PRAS40 axis and causes glomerular mesangial cell hypertrophy and matrix protein expression.

Authors:  Soumya Maity; Falguni Das; Balakuntalam S Kasinath; Nandini Ghosh-Choudhury; Goutam Ghosh Choudhury
Journal:  J Biol Chem       Date:  2020-07-30       Impact factor: 5.157

8.  Update on immunoglobulin A nephropathy, Part I: Pathophysiology.

Authors:  Maurizio Salvadori; Giuseppina Rosso
Journal:  World J Nephrol       Date:  2015-09-06

9.  Renal findings in patients with Mulibrey nanism.

Authors:  Johanna Sivunen; Susann Karlberg; Jouko Lohi; Niklas Karlberg; Marita Lipsanen-Nyman; Hannu Jalanko
Journal:  Pediatr Nephrol       Date:  2017-04-22       Impact factor: 3.714

Review 10.  Genetics of human lupus nephritis.

Authors:  Taro Iwamoto; Timothy B Niewold
Journal:  Clin Immunol       Date:  2016-09-28       Impact factor: 3.969

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