On this page
Centrioles are the microscopic cylinders that organize the cell's skeleton during division and anchor structures like cilia and flagella. These organelles play an essential role in animal cells and many lower plant cells. During cell division, the centrioles coordinate the spindle fibres that pull apart chromosome types by centromere position. When viewed in cross-section under an electron microscope, the base (or proximal end) of a centriole reveals a striking, turbine-like pattern. This is the cartwheel structure, a highly ordered scaffold that gives the centriole its distinct nine-fold symmetry.
What is the structure of centriole cartwheel triplet fibrils?
The centriole follows a "9+0" structural arrangement, meaning its wall is made of nine outer fibrils with no central microtubules (Microbe Notes, 2023). Each of these nine peripheral fibrils is a triplet microtubule. Unlike a standard isolated microtubule, which is a single tube, a triplet is formed from three joined sub-fibers called the A, B and C tubules.
Because these tubules share walls, they do not all require the same amount of building material. The structural breakdown is precise:
A-tubule: The innermost tube. It is a complete microtubule made of 13 protofilaments (chains of tubulin proteins).
B-tubule: The middle tube. It is incomplete, containing roughly 10 protofilaments of its own and sharing a wall (about 3 protofilaments) with the A-tubule.
C-tubule: The outermost tube. It is also incomplete, containing about 10 protofilaments and sharing a wall with the B-tubule.
This interlocking design means a single triplet fibril contains a total of 33 distinct protofilaments. The entire triplet is pitched at an angle of roughly 40 degrees, giving the centriole its characteristic tilted, pinwheel appearance. The resulting centriole is a robust cylinder, typically 150 to 250 nm in diameter and 300 to 700 nm long.
How does the cartwheel establish 9-fold symmetry?
Inside the ring of nine triplets lies the cartwheel itself. It acts as the assembly template when a new centriole is born.
The core of the cartwheel is the central hub, a rod-like structure roughly 25 nm in diameter. Radiating outward from this hub are nine delicate protein strands called radial spokes. At the tip of each spoke is a dense cluster called the pinhead, which binds exclusively to the complete A-tubule of a triplet fibril. This scaffolding is built primarily from a protein called SAS-6. A landmark 2007 study in *Current Biology* demonstrated that SAS-6 is the fundamental cartwheel protein that establishes this 9-fold symmetry (Nakazawa et al., 2007). The researchers found that SAS-6 dimers naturally self-assemble into a nine-sided ring. When cells are deprived of SAS-6, they struggle to build proper centrioles, often producing flawed structures with 7, 8, 10 or 11 triplets instead of the standard nine.
Visualising cellular structures
Memorising protofilament counts and protein names is a common hurdle in cell biology. Instead of relying purely on text, picturing the physical geometry of the cell makes the rules intuitive. If you are preparing for exams or untangling complex cellular mechanisms, the Fermi Concept Library maps out these structural rules from the ground up.
When you cannot quite picture how three distinct tubules fit together at a 40-degree angle, Fermi's AI tutor can draw the cross-section for you. It holds the context of your question, walks you through the transition from triplet to doublet microtubules, and tests your understanding before moving on to the next topic.
Checklist: Mapping a centriole cross-section
If you are asked to diagram or label a centriole in an exam, check your work against these key structural rules to ensure full marks:
Count the triplets: There must be exactly nine peripheral groups.
Check the overlap: The innermost ring (A) is complete. The middle (B) and outer (C) rings are incomplete C-shapes attached to the one before them.
Connect the spokes: Draw the nine radial spokes connecting the central hub to the A-tubule only.
Empty the centre: Ensure there are no isolated microtubules in the middle. The "9+0" pattern applies here.



