The Endoplasmic Reticulum (ER) is one of the most vital cell organelles found in eukaryotic cells. It is a continuous network of membranes involved in the production, modification, and transport of various substances such as proteins and lipids. Although indispensable in many cells, certain cells (like mature red blood cells) completely lack an ER. Cells that have high rates of protein or lipid production often possess an extensive endoplasmic reticulum.
There are two main types of endoplasmic reticulum in a cell:
Rough Endoplasmic Reticulum (RER)
Smooth Endoplasmic Reticulum (SER)
Below, we will explore the difference between RER and SER in points, followed by an easy-to-read table. We will also answer how the endoplasmic reticulum is important for membrane biogenesis and explain what the three differences between RER and SER are.
The endoplasmic reticulum forms a large, continuous network of flattened sacs and tubules. It extends throughout the cytoplasm, often connected to the nuclear envelope at one end and reaching out to the plasma membrane or cell periphery. This membranous network is classified into two types based on the presence or absence of ribosomes:
Rough Endoplasmic Reticulum (RER): Studded with ribosomes on its outer surface, giving it a “rough” appearance under an electron microscope.
Smooth Endoplasmic Reticulum (SER): Lacks ribosomes on its surface, resulting in a “smooth” appearance.
The ER plays a critical role in synthesising proteins, lipids, and other essential components. It also ensures that these molecules reach the correct destination within or outside the cell. Furthermore, the ER contributes to processes like membrane biogenesis, detoxification, and the formation of key organelles such as Golgi Apparatus and lysosomes.
A common question is: how is the endoplasmic reticulum important for membrane biogenesis? Membrane biogenesis refers to the process where new cellular membranes are formed from existing ones. The endoplasmic reticulum plays a pivotal role in this process in the following ways:
Lipid Synthesis: The Smooth Endoplasmic Reticulum synthesises phospholipids and cholesterol, essential building blocks of cellular membranes.
Protein Synthesis and Integration: The Rough Endoplasmic Reticulum synthesises integral membrane proteins. These proteins often remain embedded in the ER membrane before moving to other membranes (such as the Golgi or plasma membrane).
Transport of Membrane Components: Both RER and SER form transport vesicles that move membrane components to the Golgi Apparatus, which then refines and distributes them to other parts of the cell.
Thus, the endoplasmic reticulum ensures a constant supply of lipids and proteins for new membrane formation, making it crucial for maintaining and expanding various organelle membranes as cells grow or divide.
Ribosomes: The primary difference between RER and SER is the presence of ribosomes. RER has ribosomes bound to its surface, whereas SER does not.
Structure: RER is composed mainly of flattened sacs called cisternae, whereas SER predominantly consists of tubules and vesicles.
Functions:
RER is involved in protein synthesis and the initial stages of protein modification.
SER is responsible for synthesising lipids, and steroids, and also helps in carbohydrate metabolism and detoxification of certain substances.
Connection: RER is often located close to the nucleus and connected to the nuclear envelope. In contrast, SER can be found more peripherally, sometimes extending to the cell membrane.
Relationship: The SER can develop from the RER by shedding ribosomes, and it often provides vesicles that transport synthesised lipids to the Golgi Apparatus. Meanwhile, the RER provides proteins that also move to the Golgi for further processing.
If you were to narrow down the difference between RER and SER to just three key points, these would be:
Ribosomal Presence: RER has ribosomes; SER does not.
Primary Output: RER mainly produces proteins; SER mainly produces lipids and steroids.
Physical Structure: RER generally has flattened cisternae, whereas SER has tubular structures and vesicles.
These three differences encapsulate the most fundamental distinctions between these two types of endoplasmic reticulum.
To further reinforce your understanding of the difference between RER and SER, here are a few additional resources and activities:
RER: Ribosomes produce Reams of pRotein
SER: Synthesises Essential Lipids & Steroids (S-E-L-S)
1. What do ribophorins do in the RER?
a) Help in protein folding
b) Help ribosomes bind to the ER
c) Detoxify harmful substances
d) Synthesise lipids
2. Which type of ER is more common in cells specialising in lipid production?
a) RER
b) SER
c) Both RER and SER equally
d) None of the above
3. Which of the following statements about SER is incorrect?
a) SER is continuous with the nuclear envelope
b) SER lacks ribosomes
c) SER contributes to glycogen metabolism
d) SER helps synthesise lipids
Answers are highlighted for your easy reference.
1. Why do red blood cells not have an endoplasmic reticulum?
Mature red blood cells lose most of their organelles, including the nucleus and endoplasmic reticulum, to maximise space for haemoglobin. This specialised adaptation helps them transport oxygen efficiently.
2. Which part of the ER synthesises proteins, and why?
The RER synthesises proteins because it has ribosomes attached to its surface. Ribosomes decode mRNA to form polypeptide chains, which are then processed further within the RER.
3. Can the Smooth ER store substances?
Yes, in certain cells (such as muscle cells), the Smooth ER acts as a storage site for ions like calcium, which is crucial for muscle contraction.
4. Is there a functional link between RER and SER?
Absolutely. SER can bud off from RER when ribosomes detach, and they often cooperate by exchanging lipids and proteins. Together, they also send vesicles to the Golgi Apparatus for further processing.
5. Do prokaryotes have any type of endoplasmic reticulum?
Prokaryotic cells (like bacteria) do not have a true membrane-bound endoplasmic reticulum. They carry out protein and lipid synthesis using other mechanisms in the cytoplasm or on their plasma membrane.