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Extracellular renalase protects cells and organs by outside-in signalling

  • Yang Wang
  • , Robert Safirstein
  • , Heino Velazquez
  • , Xiao Jia Guo
  • , Lindsay Hollander
  • , John Chang
  • , Tian Min Chen
  • , Jian Jun Mu
  • , Gary V. Desir
  • Yale University
  • Xi'an Jiaotong University
  • University of Connecticut

Research output: Contribution to journalReview articlepeer-review

42 Scopus citations

Abstract

Renalase was discovered as a protein synthesized by the kidney and secreted in blood where it circulates at a concentration of approximately 3–5 μg/ml. Initial reports suggested that it functioned as an NAD(P)H oxidase and could oxidize catecholamines. Administration of renalase lowers blood pressure and heart rate and also protects cells and organs against ischaemic and toxic injury. Although renalase's protective effect was initially ascribed to its oxidase properties, a paradigm shift in our understanding of the cellular actions of renalase is underway. We now understand that, independent of its enzymatic properties, renalase functions as a cytokine that provides protection to cells, tissues and organs by interacting with its receptor to activate protein kinase B, JAK/STAT, and the mitogen-activated protein kinase pathways. In addition, recent studies suggest that dysregulated renalase signalling may promote survival of several tumour cells due to its capacity to augment expression of growth-related genes. In this review, we focus on the cytoprotective actions of renalase and its capacity to sustain cancer cell growth and also the translational opportunities these findings represent for the development of novel therapeutic strategies for organ injury and cancer.

Original languageEnglish
Pages (from-to)1260-1265
Number of pages6
JournalJournal of Cellular and Molecular Medicine
Volume21
Issue number7
DOIs
StatePublished - Jul 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • cell signalling
  • immune-oncology
  • ischaemic injury
  • macrophages
  • renalase
  • survival factor

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