Joints that learn to grow young
Stanford Medicine researchers identified a protein called 15-PGDH that accumulates in joints with age and gradually shuts down the cells responsible for making cartilage.
When they blocked it in old mice, cartilage grew back. When they exposed human tissue samples collected during knee replacement surgeries to the same treatment, those decades-old cells started producing new cartilage again. The mechanism is unusual: unlike most tissues, cartilage does not regrow through stem cells. Instead, the existing cartilage-producing cells, called chondrocytes, appear able to shift their gene activity and return to something like a younger state [8]. The same week, MIT Technology Review reported that Life Biosciences had just injected its first human patient, a person with glaucoma, with a treatment designed to regenerate nerve cells in the eye using a similar cellular reprogramming approach, and that the biotech sector is betting billions on this idea [114].
Stanford scientists regrow lost cartilage and reverse arthritis in major breakthrough
The 15-PGDH protein is part of a newly identified class the researchers called "gerozymes": proteins that become more active with age and suppress tissue repair across multiple systems, including muscle, bone, nerve, and blood cells. Blocking the protein in older mice didn't slow decline. It reversed it. An oral version of the drug is already in human trials for age-related muscle loss, which is the fastest path to the clinic [8].
Read the storyWhy 'reprogramming' is the buzziest approach to reversing aging right now
MIT Technology Review traced how this field went from fringe speculation to the hottest area in longevity biotech. Life Biosciences' trial is the first time a reprogramming approach has been tested in a living person. The company's chairman, David Sinclair, believes the same principle that may save one person's eyesight could eventually be applied more broadly. That's still speculative. The first trial is about glaucoma [114].
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