Eukaryotic Cells: The Endoplasmic Reticulum (A-level Biology)
Rough Endoplasmic Reticulum (RER)
- The RER contains stacked, fluid-filled membranes. The RER is a membrane bound organelle located near the nucleus. It is structurally very similar to the Golgi Apparatus. It is made up of thin, fluid filled membranes that are stacked together.
- The surface of the RER is covered in ribosomes. This is why we call it the rough endoplasmic reticulum, because it looks bumpy under a microscope. The ribosomes attached to the RER are the ribosomes that are responsible for making proteins that are meant to exported outside of the cell or to the cell surface membrane.
- The RER folds and packages proteins and sends them to the Golgi Apparatus. Proteins meant for export are made by the ribosomes and then released into the RER, which folds them and packages them and then sends them to the Golgi Apparatus. Proteins that are meant for use inside of the cell are primarily made at ribosomes that are free floating in the cytoplasm.
Smooth Endoplasmic Reticulum (SER)
- The SER does not have ribosomes. The SER is structurally similar to the RER. Except its smooth because it has no ribosomes on its surface.
- Its main function is to synthesise lipids. The SER synthesises many lipids such as cholesterol, and other molecules such as steroids and hormones for use inside the cell and for export outside of the cell. When exporting these molecules, the SER packages them and sends them to the Golgi Apparatus.
- The SER is also involved in detoxification. The SER plays a crucial role in detoxification of toxins that are either consumed by the cell, such as alcohol, or toxins produced as metabolic byproducts of metabolism.
The endoplasmic reticulum (ER) is a network of flattened sacs and tubules that is present within eukaryotic cells. It is involved in protein synthesis, lipid metabolism, and the maintenance of cellular homeostasis.
The endoplasmic reticulum can be divided into two main types: rough endoplasmic reticulum (RER) and smooth endoplasmic reticulum (SER). The RER is studded with ribosomes, which are involved in protein synthesis. The SER, on the other hand, does not have ribosomes and is involved in lipid metabolism and the detoxification of drugs and other harmful substances.
The rough endoplasmic reticulum plays a crucial role in protein synthesis by being the site of synthesis of secreted and membrane-bound proteins. The ribosomes on the surface of the RER translate the mRNA into a polypeptide chain, which is then folded and modified in the lumen of the RER before being transported to the Golgi apparatus for further processing.
The endoplasmic reticulum plays a crucial role in the maintenance of cellular homeostasis by regulating the levels of calcium ions in the cytoplasm. The SER contains calcium pumps that sequester calcium ions, preventing their levels from becoming too high and triggering cellular damage. The ER also helps to maintain the balance between the production and degradation of lipids and other cellular components.
The endoplasmic reticulum and the Golgi apparatus are closely related and work together to modify, sort, and package proteins and lipids for transport to other parts of the cell or outside the cell. Proteins and lipids are transported from the RER to the Golgi apparatus, where they are modified, sorted, and packaged into vesicles for transport to their final destination.
Yes, the endoplasmic reticulum can be involved in a number of disease processes. For example, disruptions in ER function, such as those that occur in diseases like Alzheimer’s and Huntington’s, can lead to the accumulation of misfolded proteins, which can trigger cellular damage and contribute to the progression of the disease. The ER is also involved in a number of metabolic diseases, such as type 2 diabetes, where it plays a role in insulin resistance.
The endoplasmic reticulum can be visualised in a cell by using electron microscopy or by staining the cell with special dyes. Electron microscopy provides a high-resolution image of the ER, while staining techniques, such as the ER tracker dyes, allow the ER to be visualised in living cells under a fluorescence microscope. These techniques are used by researchers to study the structure and function of the ER in different cell types and under different conditions.
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