15.3:

Role of ER in the Secretory Pathway

JoVE Core
Cell Biology
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JoVE Core Cell Biology
Role of ER in the Secretory Pathway

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01:17 min

April 30, 2023

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 in the secretory pathway are the endoplasmic reticulum, the ER-Golgi intermediate compartment, and the Golgi apparatus. Eventually, the functional protein cargo is delivered within the endomembrane system, exported out of the cell, or inserted into the plasma membrane.

Endoplasmic reticulum: the gateway to the secretory pathway

The endoplasmic reticulum is the primary gateway to the secretory pathway. It is the site where the proteins are folded, modified, and checked for quality before entering the secretory pathway. Various physiological stresses can increase the demand for secretory proteins or cause the accumulation of misfolded proteins in the ER. The disruption in the balance between protein demand and capacity to deliver correctly folded proteins in the ER causes stress.

Unchecked ER stress disturbs ER homeostasis, resulting in cellular dysfunction and disease. The primary characteristics of ER-related diseases are decreased protein folding capacity, failure to recognize and respond to misfolded proteins, and improper activation of responses to misfolded proteins. ER stress is implicated in the pathogenesis of diseases like diabetes mellitus, viral infections, and cancer.  For example, in type II diabetes mellitus, insulin resistance in the peripheral tissues of the liver results in hypersecretion of insulin by the β cells. The secretory overload experienced by the β cells skews the ER balance. It can also result in cell death in later stages of type II diabetes mellitus.