An update on the role of Hippo signaling pathway in ischemia-associated central nervous system diseases

Xuan Wei1, Guangshan Huang1, Jiyong Liu2

  • 1Key Laboratory of Hunan Province for Integrated Traditional Chinese and Western Medicine on Prevention and Treatment of Cardio-Cerebral Diseases, College of Integrated Traditional Chinese Medicine and Western Medicine, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China.

Insights

Cerebral ischemia causes significant neurological damage. Targeting the Hippo signaling pathway offers a promising therapeutic strategy for treating ischemia-associated central nervous system diseases like stroke and Alzheimer's.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Cell Biology

Background:

  • Cerebral ischemia is a leading cause of death and disability worldwide, triggering complex molecular and cellular damage in the central nervous system (CNS).
  • Neurological disorders such as ischemic stroke, Alzheimer's disease (AD), and Parkinson's disease (PD) are linked to these ischemic pathologies.
  • Current treatments for these CNS diseases are limited in their ability to specifically mitigate ischemic damage.

Purpose of the Study:

  • To explore the role of the Hippo signaling pathway in the pathogenesis of ischemia-associated CNS disorders.
  • To review recent advancements in understanding the Hippo pathway's molecular mechanisms.
  • To highlight the therapeutic potential of targeting the Hippo pathway for treating CNS diseases linked to ischemia.

Main Methods:

  • Literature review of recent studies on the Hippo signaling pathway and its involvement in CNS diseases.
  • Analysis of the molecular components and functions of the Hippo pathway (MST1/2, LATS1/2, YAP/TAZ).
  • Discussion of the pathway's role in processes like oxidative stress, inflammation, blood-brain barrier integrity, mitochondrial dysfunction, and neuronal death.

Main Results:

  • The Hippo signaling pathway regulates critical cellular processes including division, survival, and differentiation, and is involved in nervous system development.
  • Emerging evidence indicates the Hippo pathway's participation in the pathophysiology of ischemic stroke, AD, and PD.
  • The pathway is implicated in key pathological mechanisms such as oxidative stress, neuroinflammation, blood-brain barrier disruption, and neuronal apoptosis.

Conclusions:

  • Understanding the Hippo signaling pathway's molecular underpinnings is essential for developing novel therapeutic targets.
  • Targeting the Hippo signaling pathway presents a promising strategy for mitigating damage in ischemia-associated CNS diseases.
  • Further research into the Hippo pathway could lead to effective treatments for debilitating neurological conditions.