Related Experiment Video
Updated: Feb 23, 2026

Author Spotlight: Exploring the Role of Unfolded Protein Response in HIV-1 Replication and Infectivity
Published on: June 14, 2024
Coordinating Organismal Metabolism During Protein Misfolding in the ER Through the Unfolded Protein Response
Vishwanatha K Chandrahas1, Jaeseok Han2, Randal J Kaufman3
1Degenerative Diseases Program, Sanford_Burnham_Prebys Medical Discovery Institute, 92037, La Jolla, CA, USA.
Abstract:
The endoplasmic reticulum (ER) is a cellular organelle responsible for folding of secretory and membrane proteins. Perturbance in ER homeostasis caused by various intrinsic/extrinsic stimuli challenges the protein-folding capacity of the ER, leading to an ER dysfunction, called ER stress. Cells have developed a defensive response to adapt and/or survive in the face of ER stress that may be detrimental to cell function and survival. When exposed to ER stress, the cell activates a complex and elaborate signaling network that includes translational modulation and transcriptional induction of genes. In addition to these autonomous responses, recent studies suggest that the stressed tissue secretes peptides or unknown factors that transfer the signal to other cells in the same or different organs, leading the organism as a whole to cope with challenges in a non-autonomous manner. In this review, we discuss the mechanisms by which cells adapt to ER stress challenges autonomously and transfer the stress signal to non-stressed cells in different organs.
Related Concept Videos
The Unfolded Protein Response
Regulation of the Unfolded Protein Response
Export of Misfolded Proteins out of the ER
Protein Folding Quality Check in the RER
Protein Modifications in the RER
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal...
Molecular Chaperones and Protein Folding
The...

