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Regulation of the Unfolded Protein Response01:31

Regulation of the Unfolded Protein Response

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Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
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Role of ER in the Secretory Pathway01:17

Role of ER in the Secretory Pathway

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Eukaryotic cells have a special pathway that enables communication between various intracellular membrane-bound compartments and also with the extracellular environment. This pathway is termed as the secretory pathway.
Components of the secretory pathway
About a third of proteins synthesized in the cell are sorted via the secretory route. They shuffle between different compartments in membrane-bound vesicles until they reach their final destination. The main intracellular compartments involved...
5.3K
The Unfolded Protein Response01:37

The Unfolded Protein Response

4.4K
The ER is the hub of protein synthesis in a cell. It has robust systems to quality control protein folding and also for degradation of terminally misfolded proteins. Under normal conditions, a small proportion of misfolded proteins that cannot be salvaged need to be transported to the cytoplasm by the ER-associated degradation or ERAD pathways. However, if the ERAD cannot handle the misfolded proteins, the cell activates the unfolded protein response or UPR to adjust the protein folding...
4.4K
Export of Misfolded Proteins out of the ER01:32

Export of Misfolded Proteins out of the ER

3.5K
After folding, the ER assesses the quality of secretory and membrane proteins. The correctly folded proteins are cleared by the calnexin cycle for transport to their final destination, while misfolded proteins are held back in the ER lumen. The ER chaperones attempt to unfold and refold the misfolded proteins but sometimes fail to achieve the correct native conformation. Such terminally misfolded proteins are then exported to the cytosol by ER-associated degradation or ERAD pathway for...
3.5K
Endoplasmic Reticulum01:39

Endoplasmic Reticulum

94.1K
The Endoplasmic Reticulum (ER) in eukaryotic cells is a substantial network of interconnected membranes with diverse functions, from calcium storage to biomolecule synthesis. A primary component of the endomembrane system, the ER manufactures phospholipids critical for membrane function throughout the cell. Additionally, the two distinct regions of the ER specialize in the manufacture of specific lipids and proteins.
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Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

5.6K
Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
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Related Experiment Video

Updated: Jun 6, 2025

Molecular Modulation by Lentivirus-Delivered Specific shRNAs in Endoplasmic Reticulum Stressed Neurons
10:50

Molecular Modulation by Lentivirus-Delivered Specific shRNAs in Endoplasmic Reticulum Stressed Neurons

Published on: April 24, 2021

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Exploring Endocannabinoid System: Unveiling New Roles in Modulating ER Stress.

Ilaria Capolupo1,2, Maria Rosaria Miranda1,2,3, Simona Musella1

  • 1Department of Pharmacy, University of Salerno, Via G. Paolo II, Fisciano, 84084 Salerno, Italy.

Antioxidants (Basel, Switzerland)
|November 27, 2024
PubMed
Summary

The endocannabinoid system (ECS) helps restore cellular balance by regulating endoplasmic reticulum (ER) stress. Cannabinoid receptor (CB) activation by ECS components mitigates ER stress and inflammation.

Keywords:
ER stresscancercannabinoidsmetabolic disordersneurodegenerative diseaseoxidative stress

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Area of Science:

  • Cellular Biology
  • Molecular Medicine
  • Neuroscience

Background:

  • Endoplasmic reticulum (ER) dysfunction causes diseases like cancer and neurodegeneration via ER stress.
  • ER stress involves complex cellular responses impacting homeostasis.
  • Understanding ER failure mechanisms is crucial for disease intervention.

Purpose of the Study:

  • To review the role of the endocannabinoid system (ECS) in modulating ER stress.
  • To explore the interaction between ER stress and cannabinoid receptors (CB).
  • To highlight mechanisms of natural cannabinoids in regulating cellular stress responses.

Main Methods:

  • Literature review focusing on ER stress and the ECS.
  • Analysis of studies on cannabinoid receptor (CB) activation and its downstream effects.
  • Examination of cellular pathways including UPR and oxidative stress response.

Main Results:

  • CB activation by the ECS can restore ER homeostasis.
  • CBs regulate key ER stress markers like PERK, ATF6, and IRE1.
  • ECS signaling exhibits anti-inflammatory effects linked to ER stress resolution.

Conclusions:

  • The ECS plays a significant role in managing ER stress.
  • Targeting CBs offers potential therapeutic strategies for ER stress-related disorders.
  • Further research into natural cannabinoids' modulation of ER stress is warranted.