Roles for endoplasmic reticulum-associated degradation and the novel endoplasmic reticulum stress response gene derlin-3 in the ischemic heart

Peter J. Belmont, Wenqiong J. Chen, Matthew N. San Pedro, Donna J. Thuerauf, Nicole Gellings Lowe, Natalie Gude, Brett Hilton, Roland Wolkowicz, Mark A. Sussman, Christopher C. Glembotski

Research output: Contribution to journalArticlepeer-review

61 Scopus citations

Abstract

Rationale: Stresses, such as ischemia, impair folding of nascent proteins in the rough endoplasmic reticulum (ER), activating the unfolded protein response, which restores efficient ER protein folding, thus leading to protection from stress. In part, the unfolded protein response alleviates ER stress and cell death by increasing the degradation of terminally misfolded ER proteins via ER-associated degradation (ERAD). ERAD is increased by the ER stress modulator, activating transcription factor (ATF)6, which can induce genes that encode components of the ERAD machinery. Objective: Recently, it was shown that the mouse heart is protected from ischemic damage by ATF6; however, ERAD has not been studied in the cardiac context. A recent microarray study showed that the Derlin-3 (Derl3) gene, which encodes an important component of the ERAD machinery, is robustly induced by ATF6 in the mouse heart. Methods and Results: In the present study, activated ATF6 induced Derl3 in cultured cardiomyocytes, and in the heart, in vivo. Simulated ischemia (sI), which activates ER stress, induced Derl3 in cultured myocytes, and in an in vivo mouse model of myocardial infarction, Derl3 was also induced. Derl3 overexpression enhanced ERAD and protected cardiomyocytes from simulated ischemia-induced cell death, whereas dominant-negative Derl3 decreased ERAD and increased simulated ischemia-induced cardiomyocyte death. Conclusions: This study describes a potentially protective role for Derl3 in the heart, and is the first to investigate the functional consequences of enhancing ERAD in the cardiac context.

Original languageEnglish (US)
Pages (from-to)307-316
Number of pages10
JournalCirculation research
Volume106
Issue number2
DOIs
StatePublished - Feb 2010
Externally publishedYes

Keywords

  • Endoplasmic reticulum stress
  • Endoplasmic reticulum-associated degradation
  • Ischemia
  • Unfolded protein response

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

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