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The regulation and function of the Hippo pathway in heart regeneration

出版社

WILEY
DOI: 10.1002/wdev.335

关键词

heart failure; heart regeneration; Hippo pathway; mechanical stress; ROS

资金

  1. National Institutes of Health [DE 023177, HL 127717, HL 130804, HL 118761]
  2. Vivian L. Smith Foundation
  3. LeDucq Foundation's Transatlantic Networks of Excellence in Cardiovascular Research [14CVD01]
  4. MacDonald Research Fund Award [16RDM001]
  5. Saving tiny Hearts Society
  6. American Heart Association postdoctoral fellowship [18POST34060186]

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Heart failure caused by cardiomyocyte loss and fibrosis is a leading cause of death worldwide. Although current treatments for heart failure such as heart transplantation and left ventricular assist device implantation have obvious value, new approaches are needed. Endogenous adult cardiomyocyte renewal is measurable but inefficient and inadequate in response to extensive acute heart damage. Stimulating self-renewal of endogenous cardiomyocytes holds great promise for heart repair. Uncovering the genetic mechanisms underlying cardiomyocyte renewal is a critical step in developing new approaches to repairing the heart. Recent studies have revealed that the inhibition of the Hippo pathway is sufficient to promote the proliferation of endogenous cardiomyocytes, indicating that the manipulation of the Hippo pathway in the heart may be a promising treatment for heart failure in the future. We summarize recent findings that have shed light on the function of the Hippo pathway in heart regeneration. We also discuss the mechanisms by which Hippo pathway inhibition promotes heart regeneration and how the Hippo pathway responds to different types of injury or stress during the regenerative process. This article is categorized under: Adult Stem Cells, Tissue Renewal, and Regeneration > Regeneration

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