Literature DB >> 25608752

Plasticity of renal endocrine function.

Birgül Kurt1, Armin Kurtz2.   

Abstract

The kidneys are important endocrine organs. They secrete humoral factors, such as calcitriol, erythropoietin, klotho, and renin into the circulation, and therefore, they are essentially involved in the regulation of a variety of processes ranging from bone formation to erythropoiesis. The endocrine functions are established by cells, such as proximal or distal tubular cells, renocortical interstitial cells, or mural cells of afferent arterioles. These endocrine cells are either fixed in number, such as tubular cells, which individually and gradually upregulate or downregulate hormone production, or they belong to a pool of cells, which display a recruitment behavior, such as erythropoietin- and renin-producing cells. In the latter case, regulation of humoral function occurs via (de)recruitment of active endocrine cells. As a consequence renin- and erythropoietin-producing cells in the kidney show a high degree of plasticity by reversibly switching between distinct cell states. In this review, we will focus on the characteristics of renin- and of erythropoietin-producing cells, especially on their origin and localization, their reversible transformations, and the mediators, which are responsible for transformation. Finally, we will discuss a possible interconversion of renin and erythropoietin expression.
Copyright © 2015 the American Physiological Society.

Entities:  

Keywords:  calcitriol; erythropoietin; klotho; renin

Mesh:

Substances:

Year:  2015        PMID: 25608752     DOI: 10.1152/ajpregu.00568.2013

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  7 in total

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Authors:  Sahar Rostami Mansoor; Abdolamir Allameh; Hadi Parsian
Journal:  J Mol Neurosci       Date:  2018-06-06       Impact factor: 3.444

2.  Zebrafish mesonephric renin cells are functionally conserved and comprise two distinct morphological populations.

Authors:  Sebastien A Rider; Helen C Christian; Linda J Mullins; Amelia R Howarth; Calum A MacRae; John J Mullins
Journal:  Am J Physiol Renal Physiol       Date:  2017-02-08

3.  Renalase attenuates hypertension, renal injury and cardiac remodelling in rats with subtotal nephrectomy.

Authors:  Jianyong Yin; Zeyuan Lu; Feng Wang; Zhenzhen Jiang; Limin Lu; Naijun Miao; Niansong Wang
Journal:  J Cell Mol Med       Date:  2016-02-29       Impact factor: 5.310

4.  Sodium fluoride induces nephrotoxicity via oxidative stress-regulated mitochondrial SIRT3 signaling pathway.

Authors:  Chao Song; Beibei Fu; Jingcheng Zhang; Jiamin Zhao; Mengke Yuan; Wei Peng; Yong Zhang; Haibo Wu
Journal:  Sci Rep       Date:  2017-04-06       Impact factor: 4.379

Review 5.  Cross-talks between the kidneys and the central nervous system in multiple sclerosis.

Authors:  Sahar Rostami; Mohammad-Sajad Emami-Aleagha; Maryam Ghasemi-Kasman; Abdolamir Allameh
Journal:  Caspian J Intern Med       Date:  2018

Review 6.  Renal hypoxia-HIF-PHD-EPO signaling in transition metal nephrotoxicity: friend or foe?

Authors:  Frank Thévenod; Timm Schreiber; Wing-Kee Lee
Journal:  Arch Toxicol       Date:  2022-04-21       Impact factor: 6.168

7.  Dysregulated mesenchymal PDGFR-β drives kidney fibrosis.

Authors:  Eva M Buhl; Sonja Djudjaj; Barbara M Klinkhammer; Katja Ermert; Victor G Puelles; Maja T Lindenmeyer; Clemens D Cohen; Chaoyong He; Erawan Borkham-Kamphorst; Ralf Weiskirchen; Bernd Denecke; Panuwat Trairatphisan; Julio Saez-Rodriguez; Tobias B Huber; Lorin E Olson; Jürgen Floege; Peter Boor
Journal:  EMBO Mol Med       Date:  2020-01-14       Impact factor: 12.137

  7 in total

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