TY - JOUR
T1 - New concepts of endoplasmic reticulum function in the heart
T2 - Programmed to conserve
AU - Doroudgar, Shirin
AU - Glembotski, Christopher C.
N1 - Funding Information:
Research in the Glembotski lab is supported by National Institutes of Health , grants HL-075573 , HL-085577 , and HL104535 to CCG, and by grants and fellowships to SD from the SDSU Heart Institute, the Rees-Stealy Research Foundation , the San Diego Chapter of the Achievement Rewards for College Scientists (ARCS) Foundation , the American Heart Association (Predoctoral Fellowship 10PRE3410005 ), and the Inamori Foundation to SD.
PY - 2013/2
Y1 - 2013/2
N2 - Secreted and membrane proteins play critical roles in myocardial health and disease. Studies in non-myocytes have shown that the peri-nuclear ER is the site for synthesis, folding, and quality control of most secreted and membrane proteins, as well as a nexus of a signal transduction system, called the ER stress response, which informs the cell about the status of ER protein folding. Moreover, the dynamic physical and functional association of the ER with mitochondria is a key site responsible for integrating ER function and mitochondrial metabolism, but is only just beginning to be understood in the myocardium. Although a great deal is known about roles played by the sarcoplasmic reticulum (SR) in contractile calcium handling in the heart, little is known about the relative locations and functions of the peri-nuclear ER and the SR in terms of secreted and membrane protein synthesis and folding. In this review we will explore the current state of knowledge of the location of secreted and membrane protein synthesis, folding, and quality control machinery in cardiac myocytes, as well as our understanding of the functional consequences of ER stress and the unfolded protein response in the heart in terms of protein synthesis, cell growth, and metabolic regulation. This article is part of a Special Issue entitled "Focus on Cardiac Metabolism".
AB - Secreted and membrane proteins play critical roles in myocardial health and disease. Studies in non-myocytes have shown that the peri-nuclear ER is the site for synthesis, folding, and quality control of most secreted and membrane proteins, as well as a nexus of a signal transduction system, called the ER stress response, which informs the cell about the status of ER protein folding. Moreover, the dynamic physical and functional association of the ER with mitochondria is a key site responsible for integrating ER function and mitochondrial metabolism, but is only just beginning to be understood in the myocardium. Although a great deal is known about roles played by the sarcoplasmic reticulum (SR) in contractile calcium handling in the heart, little is known about the relative locations and functions of the peri-nuclear ER and the SR in terms of secreted and membrane protein synthesis and folding. In this review we will explore the current state of knowledge of the location of secreted and membrane protein synthesis, folding, and quality control machinery in cardiac myocytes, as well as our understanding of the functional consequences of ER stress and the unfolded protein response in the heart in terms of protein synthesis, cell growth, and metabolic regulation. This article is part of a Special Issue entitled "Focus on Cardiac Metabolism".
KW - ER stress response
KW - Endoplasmic reticulum
KW - Folding
KW - Protein synthesis
KW - Quality control
KW - Sarcoplasmic reticulum
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U2 - 10.1016/j.yjmcc.2012.10.006
DO - 10.1016/j.yjmcc.2012.10.006
M3 - Review article
C2 - 23085588
AN - SCOPUS:84872683707
SN - 0022-2828
VL - 55
SP - 85
EP - 91
JO - Journal of Molecular and Cellular Cardiology
JF - Journal of Molecular and Cellular Cardiology
IS - 1
ER -