Why Could a Tendon Be Used to Replace a Ligament?

Tendons and ligaments are dense, fibrous connective tissues with distinct roles in the musculoskeletal system. Tendons function as the interface between muscle and bone, transferring the force generated by muscle contraction to create movement. Ligaments connect one bone to another, stabilizing joints and limiting excessive motion. When a ligament suffers a complete rupture, such as a severe tear of the anterior cruciate ligament (ACL), it often requires surgical reconstruction because it cannot heal robustly. Surgeons commonly use a piece of tendon tissue as a biological substitute to restore the joint’s stability.

Fundamental Differences in Tissue Composition

Both tendons and ligaments are primarily composed of Type I collagen protein, which gives them high tensile strength and a degree of stiffness. The arrangement of these collagen fibers is a key difference reflecting their separate functions. Tendons are structured to manage high, unidirectional pulling forces, aligning their collagen fibers in a dense, parallel fashion. Ligaments must resist forces from multiple directions to stabilize a joint through its range of motion.

Ligaments have a slightly less parallel, more interwoven organization of collagen fibers, sometimes including elastin for greater stretch. Both tissues have low vascularity, meaning they have a poor blood supply compared to muscle tissue. This limited blood flow is why severe ligament injuries, like a complete ACL tear, often fail to repair themselves effectively, necessitating a replacement graft.

Load-Bearing Requirements and Tensile Strength

The decision to use a tendon graft is based on matching the replacement tissue’s strength to the demands of the original ligament. Tendons are engineered to withstand immense tensile forces as they transmit muscle contraction power to the skeleton. The tight, parallel bundling of Type I collagen fibers within the tendon provides this exceptional longitudinal strength. Their ultimate tensile strength, ranging from 50 to 150 megapascals, makes them highly durable.

A replacement ligament, especially in a high-demand joint like the knee, must possess similar high tensile strength to prevent re-rupture. The tendon’s parallel fiber orientation provides the immediate “time zero” strength needed after surgery. This allows the graft to immediately take on the high directional forces required to stabilize the joint. The stiffness characteristics of the tendon, which relate to its resistance to stretching under tension, are well-suited to act as an immediate mechanical restraint within the joint.

The Graft Transformation Process

After implantation, the tendon undergoes a complex biological process known as “ligamentization,” necessary for it to functionally adapt to its new role. The process begins with necrosis, where tendon cells die due to blood supply loss upon transplantation; subsequently, the graft is revascularized, and new cells repopulate the tissue. The replacement tissue enters a proliferative phase, changing structurally and biologically as it shifts from a tendon-like to a ligament-like structure. Over many months, new collagen is synthesized and remodeled under the mechanical stresses within the joint. The collagen fibers, initially aligned strictly in parallel, begin to reorient themselves into a more complex, interwoven pattern, allowing the former tendon to better resist multi-directional forces. This slow process often takes 1 to 3 years to reach a mature, stable state resembling the native ligament.

Where Replacement Tendons Come From

The source of the replacement tendon material is categorized based on its origin. An autograft uses tissue harvested from the patient’s own body, frequently taken from the hamstring, patellar, or quadriceps tendons. Autografts are desirable because they are the patient’s own living tissue, resulting in faster incorporation and carrying no risk of disease transmission or immune rejection.

The primary drawback of an autograft is donor site morbidity, which includes pain, weakness, or complication at the removal site. Alternatively, an allograft uses tendon tissue from a deceased human donor, such as the Achilles or tibialis anterior tendon. Allografts eliminate donor site morbidity and shorten surgical time but involve a risk of slower integration and a very small, though managed, risk of disease transmission.