4.5 Review

The role of autophagy in death of cardiomyocytes

Journal

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
Volume 165, Issue -, Pages 1-8

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.yjmcc.2021.12.006

Keywords

Autophagy; Cell death; Autosis; Cardiomyocytes; Cardiac glycosides

Funding

  1. U.S. Public Health Service [HL67724, HL91469, HL102738, HL112330, HL138720, HL144626, HL150881, AG23039]
  2. American Heart Association Merit Award 20 Merit [35120374]
  3. Fondation Leducq Trans-atlantic Network of Excellence [15CVD04]

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Autophagy is a cellular process that helps maintain cellular quality control and energy homeostasis by degrading cellular materials through the lysosomes. It can either adaptively help cells survive stressful conditions or mediate cell death during development and stress response. Dysregulation of autophagy can lead to accumulation of autophagosomes, causing cellular dysfunction and death. In the heart, dysregulated autophagy is associated with cardiomyocyte death and cardiac injury.
Autophagy mediates cellular quality control mechanisms and energy homeostasis through lysosomal degradation. Autophagy is typically viewed as an adaptive process that allows cells to survive against stress, such as nutrient deprivation and hypoxia. However, autophagy also mediates cell death during development and in response to stress. Cell death accompanied by autophagy activation and accumulation of autophagosomes has been classified as type II programmed cell death. Compared to the wealth of knowledge regarding the adaptive role of autophagy, however, the molecular mechanisms through which autophagy induces cell death and its functional significance are poorly understood. Autophagy is activated excessively under some conditions, causing uncontrolled degradation of cellular materials and cell death. An imbalance between autophagosome formation and lysosomal degradation causes a massive accumulation of autophagosomes, which subsequently causes cellular dysfunction and death. Dysregulation of autophagy induces a unique form of cell death, termed autosis, with defined morphological and biochemical features distinct from other forms of programmed cell death, such as apoptosis and necrosis. In the heart, dysregulated autophagy induces death of cardiomyocytes and actively mediates cardiac injury and dysfunction in some conditions, including reperfusion injury, doxorubicin cardiomyopathy, and lysosomal storage disorders. The goal in this review is to introduce the concept of autophagic cell death and discuss its functional significance in various cardiac conditions.

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