Inhibition of Mutant αB Crystallin-Induced Protein Aggregation by a Molecular Tweezer.

Abstract

BACKGROUND:

Compromised protein quality control causes the accumulation of misfolded proteins and intracellular aggregates, contributing to cardiac disease and heart failure. The development of therapeutics directed at proteotoxicity-based pathology in heart disease is just beginning. The molecular tweezer CLR01 is a broad-spectrum inhibitor of abnormal self-assembly of amyloidogenic proteins, including amyloid β-protein, tau, and α-synuclein. This small molecule interferes with aggregation by binding selectively to lysine side chains, changing the charge distribution of aggregation-prone proteins and thereby disrupting aggregate formation. However, the effects of CLR01 in cardiomyocytes undergoing proteotoxic stress have not been explored. Here we assess whether CLR01 can decrease cardiac protein aggregation catalyzed by cardiomyocyte-specific expression of mutated αB-crystallin (CryABR120G).

METHODS AND RESULTS:

A proteotoxic model of desmin-related cardiomyopathy caused by cardiomyocyte-specific expression of CryABR120G was used to test the efficacy of CLR01 therapy in the heart. Neonatal rat cardiomyocytes were infected with adenovirus expressing either wild-type CryAB or CryABR120G. Subsequently, the cells were treated with different doses of CLR01 or a closely related but inactive derivative, CLR03. CLR01 decreased aggregate accumulation and attenuated cytotoxicity caused by CryABR120G expression in a dose-dependent manner, whereas CLR03 had no effect. Ubiquitin-proteasome system function was analyzed using a ubiquitin-proteasome system reporter protein consisting of a short degron, CL1, fused to the COOH-terminus of green fluorescent protein. CLR01 improved proteasomal function in CryABR120G cardiomyocytes but did not alter autophagic flux. In vivo, CLR01 administration also resulted in reduced protein aggregates in CryABR120G transgenic mice.

CONCLUSIONS:

CLR01 can inhibit CryABR120G aggregate formation and decrease cytotoxicity in cardiomyocytes undergoing proteotoxic stress, presumably through clearance of the misfolded protein via increased proteasomal function. CLR01 or related compounds may be therapeutically useful in treating the pathogenic sequelae resulting from proteotoxic heart disease.

• Authors: Na Xu, Gal Bitan, Thomas Schrader, Frank-Gerrit Klärner, Hanna Osinska, Jeffrey Robbins
• Journal: Journal of the American Heart Association (J Am Heart Assoc) Vol. 6 Issue 8 (Aug 08 2017) ISSN: 2047-9980 [Electronic] England
• PMID: 28862927 (Publication Type: Journal Article)
• Copyright: © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

Chemical References

• Bridged-Ring Compounds
• CLR01 compound
• CLR03 compound
• Organophosphates
• Organophosphorus Compounds
• Protein Aggregates
• alpha-Crystallin B Chain
• Proteasome Endopeptidase Complex

Topics

• Adenoviridae (genetics)
• Animals
• Bridged-Ring Compounds (pharmacology)
• Cells, Cultured
• Dose-Response Relationship, Drug
• Genetic Vectors
• Mice, Transgenic
• Mutation
• Myocytes, Cardiac (drug effects, metabolism, pathology)
• Organophosphates (pharmacology)
• Organophosphorus Compounds (pharmacology)
• Proteasome Endopeptidase Complex (metabolism)
• Protein Aggregates
• Protein Aggregation, Pathological
• Protein Folding
• Proteolysis
• Rats
• Rats, Sprague-Dawley
• Time Factors
• Transduction, Genetic
• Transfection
• Ubiquitination
• alpha-Crystallin B Chain (genetics, metabolism)