Atg7 induces basal autophagy and rescues autophagic deficiency in CryABR120G cardiomyocytes

J. Scott Pattison, Hanna Osinska, Jeffrey Robbins

Research output: Contribution to journalArticle

105 Citations (Scopus)

Abstract

RATIONALE: Increasing evidence suggests that misfolded proteins and intracellular aggregates contribute to cardiac disease and heart failure. Several cardiomyopathies, including the αB-crystallin R120G mutation (CryABR102G) model of desmin-related cardiomyopathy, accumulate cytotoxic misfolded proteins in the form of preamyloid oligomers and aggresomes. Impaired autophagic function is a potential cause of misfolded protein accumulations, cytoplasmic aggregate loads, and cardiac disease. Atg7, a mediator of autophagosomal biogenesis, is a putative regulator of autophagic function. OBJECTIVE: To determine whether autophagic induction by Atg7 is sufficient to reduce misfolded protein and aggregate content in protein misfolding-stressed cardiomyocytes. METHODS AND RESULTS: To define the gain and loss of function effects of Atg7 expression on CryABR102G protein misfolding and aggregates, neonatal rat cardiomyocytes were infected with adenoviruses expressing either wild-type CryABR102G or CryAB R102G and coinfected with Atg7 adenovirus or with Atg7 silencing siRNAs to produce gain-of or loss-of Atg7 function. Atg7 overexpression effectively induced basal autophagy with no detrimental effects on cell survival, suggesting that Atg7 can activate autophagy with no apparent cytotoxic effects. Autophagic flux assays on CryAB-expressing cardiomyocytes revealed reduced autophagic function, which probably contributed to the failure of misfolded proteins and aggregates to be cleared. Coexpression of Atg7 and CryABR102G significantly reduced preamyloid oligomer staining, aggregate content, and cardiomyocyte cytotoxicity. Conversely, Atg7 silencing in the CryABR102G background significantly inhibited the already reduced rate of autophagy and increased CryABR102G aggregate content and cytotoxicity. CONCLUSIONS: Atg7 induces basal autophagy, rescues the CryABR102G autophagic deficiency, and attenuates the accumulation of misfolded proteins and aggregates in cardiomyocytes.

Original languageEnglish (US)
Pages (from-to)151-160
Number of pages10
JournalCirculation Research
Volume109
Issue number2
DOIs
StatePublished - Jul 8 2011

Fingerprint

Autophagy
Cardiac Myocytes
Cardiomyopathies
Adenoviridae
Heart Diseases
Heart Failure
Crystallins
Proteins
Desmin
Cell Survival
Protein Aggregates
Staining and Labeling
Mutation

Keywords

  • Atg7
  • aggregate
  • amyloid
  • autophagy

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Atg7 induces basal autophagy and rescues autophagic deficiency in CryABR120G cardiomyocytes. / Pattison, J. Scott; Osinska, Hanna; Robbins, Jeffrey.

In: Circulation Research, Vol. 109, No. 2, 08.07.2011, p. 151-160.

Research output: Contribution to journalArticle

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abstract = "RATIONALE: Increasing evidence suggests that misfolded proteins and intracellular aggregates contribute to cardiac disease and heart failure. Several cardiomyopathies, including the αB-crystallin R120G mutation (CryABR102G) model of desmin-related cardiomyopathy, accumulate cytotoxic misfolded proteins in the form of preamyloid oligomers and aggresomes. Impaired autophagic function is a potential cause of misfolded protein accumulations, cytoplasmic aggregate loads, and cardiac disease. Atg7, a mediator of autophagosomal biogenesis, is a putative regulator of autophagic function. OBJECTIVE: To determine whether autophagic induction by Atg7 is sufficient to reduce misfolded protein and aggregate content in protein misfolding-stressed cardiomyocytes. METHODS AND RESULTS: To define the gain and loss of function effects of Atg7 expression on CryABR102G protein misfolding and aggregates, neonatal rat cardiomyocytes were infected with adenoviruses expressing either wild-type CryABR102G or CryAB R102G and coinfected with Atg7 adenovirus or with Atg7 silencing siRNAs to produce gain-of or loss-of Atg7 function. Atg7 overexpression effectively induced basal autophagy with no detrimental effects on cell survival, suggesting that Atg7 can activate autophagy with no apparent cytotoxic effects. Autophagic flux assays on CryAB-expressing cardiomyocytes revealed reduced autophagic function, which probably contributed to the failure of misfolded proteins and aggregates to be cleared. Coexpression of Atg7 and CryABR102G significantly reduced preamyloid oligomer staining, aggregate content, and cardiomyocyte cytotoxicity. Conversely, Atg7 silencing in the CryABR102G background significantly inhibited the already reduced rate of autophagy and increased CryABR102G aggregate content and cytotoxicity. CONCLUSIONS: Atg7 induces basal autophagy, rescues the CryABR102G autophagic deficiency, and attenuates the accumulation of misfolded proteins and aggregates in cardiomyocytes.",
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