The confocal image shows chondrogenic progenitor cells migrating into the cartilage injury site in response to the stromal cell-derived factor 1(SDF1) contained in the hydrogel; © UI Health Care
A University of Iowa orthopedics research team is working on a solution with hopes it will result in a minimally invasive, practical, and inexpensive approach for repairing cartilage and preventing osteoarthritis.
Knee injuries are the bane of athletes everywhere. Current surgical options for repairing damaged cartilage caused by knee injuries are costly, can have complications, and often are not very effective in the long run. Even after surgery, cartilage degeneration can progress leading to painful arthritis.
"We are creating an hydrogel that can repair cartilage damage, regenerate stronger cartilage, and hopefully delay or eliminate the development of osteoarthritis and eliminate the need for total knee replacement," says Yin Yu, a graduate student in the lab of James Martin, PhD, UI assistant professor of orthopedics and rehabilitation. Yu is first author of the study, which is featured on the cover of the May issue of the journal Arthritis and Rheumatology.
Martin's team had previously identified precursor cells within normal cartilage that can mature into new cartilage tissue. This was a surprising discovery because of the long-held assumption that cartilage is one of the few tissues in the body that cannot repair itself.
The team also identified molecular signaling factors that attract these precursor cells, known as chondrogenic progenitor cells (CPC), out of the surrounding healthy tissue into the damaged area and cause them to develop into new, normal cartilage. One of the signals, called stromal cell-derived factor 1 (SDF1), acts like a homing beacon for the precursor cells.
In an experimental model of cartilage injury, Yu loaded the custom-made hydrogel with SDF1 and injected it into holes punched into the model cartilage. The precursor cells migrated toward the SDF1 signal and filled in the injury site. Subsequent application of a growth factor caused the cells to mature into normal cartilage that repaired the injury.
"This process gives us a great result," Yu says. "The new cartilage integrates seamlessly with the undamaged tissue, it has normal concentrations of proteoglycans, good structural properties, and looks like normal cartilage."
The new tissue is not as mechanically strong as normal cartilage, but Yu and Martin think that mechanical loading - the type of stress that is exerted during physical therapy and exercise - might improve the mechanical properties.
"There's really no cure for osteoarthritis except for total joint replacement, which is not particularly suitable for younger patients because the artificial joints wear out and need to be replaced multiple times," says Martin. "Our approach aims to leverage the body's own capacity for repair, and what we've shown is that cartilage does have regenerative potential; you just have to manipulate it just right."
To translate this approach into a therapy that can be used in people, the team now needs to include the growth factor in the gel in such a way that there is a stepwise release of the attractant SDF1 followed by the growth factor.
Yu and Martin plan to start animal trials within a year and, if the results are good, they hope to be ready to start human trials in about five years.
MEDICA-tradefair.com; Source: University of Iowa Health Care