ER stress-induced secretion of proteins and their extracellular functions in the heart
Endoplasmic reticulum (ER) stress is a result of conditions that imbalance protein homeostasis or proteostasis at the ER, for example ischemia, and is a common event in various human pathologies, including the diseased heart. Cardiac integrity and function depend on the active secretion of mature pr...
Gespeichert in:
| Hauptverfasser: | , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
10 September 2020
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| In: |
Cells
Year: 2020, Jahrgang: 9, Heft: 9 |
| ISSN: | 2073-4409 |
| DOI: | 10.3390/cells9092066 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/cells9092066 Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2073-4409/9/9/2066 |
| Verfasserangaben: | Bianca A. Meyer and Shirin Doroudgar |
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| 520 | |a Endoplasmic reticulum (ER) stress is a result of conditions that imbalance protein homeostasis or proteostasis at the ER, for example ischemia, and is a common event in various human pathologies, including the diseased heart. Cardiac integrity and function depend on the active secretion of mature proteins from a variety of cell types in the heart, a process that requires an intact ER environment for efficient protein folding and trafficking to the secretory pathway. As a consequence of ER stress, most protein secretion by the ER secretory pathway is decreased. Strikingly, there is a select group of proteins that are secreted in greater quantities during ER stress. ER stress resulting from the dysregulation of ER Ca2+ levels, for instance, stimulates the secretion of Ca2+-binding ER chaperones, especially GRP78, GRP94, calreticulin, and mesencephalic astrocyte-derived neurotrophic factor (MANF), which play a multitude of roles outside the cell, strongly depending on the cell type and tissue. Here we review current insights in ER stress-induced secretion of proteins, particularly from the heart, and highlight the extracellular functions of these proteins, ranging from the augmentation of cardiac cell viability to the modulation of pro- and anti-apoptotic, oncogenic, and immune-stimulatory cell signaling, cell invasion, extracellular proteostasis, and more. Many of the roles of ER stress-induced protein secretion remain to be explored in the heart. This article is part of a special issue entitled “The Role of Proteostasis Derailment in Cardiac Diseases.” | ||
| 650 | 4 | |a cardiac myocytes | |
| 650 | 4 | |a cardiokines | |
| 650 | 4 | |a cell signaling | |
| 650 | 4 | |a ER stress | |
| 650 | 4 | |a protein secretion | |
| 650 | 4 | |a proteostasis | |
| 650 | 4 | |a secreted ER chaperones | |
| 650 | 4 | |a unfolded protein response (UPR) | |
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