Human Migratory Meniscus Progenitor Cells Are Controlled via the TGF-β Pathway

Summary

Degeneration of the knee joint during osteoarthritis often begins with meniscal lesions. Meniscectomy, previously performed extensively after meniscal injury, is now obsolete because of the inevitable osteoarthritis that occurs following this procedure. Clinically, meniscus self-renewal is well documented as long as the outer, vascularized meniscal ring remains intact. In contrast, regeneration of the inner, avascular meniscus does not occur. Here, we show that cartilage tissue harvested from the avascular inner human meniscus during the late stages of osteoarthritis harbors a unique progenitor cell population. These meniscus progenitor cells (MPCs) are clonogenic and multipotent and exhibit migratory activity. We also determined that MPCs are likely to be controlled by canonical transforming growth factor β (TGF-β) signaling that leads to an increase in SOX9 and a decrease in RUNX2, thereby enhancing the chondrogenic potential of MPC. Therefore, our work is relevant for the development of novel cell biological, regenerative therapies for meniscus repair.

Graphical Abstract

Highlights

• •

  Progenitor cells are found in the inner avascular part of human osteoarthritic menisci

• •

  These meniscus progenitor cells (MPCs) are clonogenic, migratory, and multipotent

• •

  MPCs are governed via the canonical TGF-β pathway

• •

  TGF-β3 via Smad2 reduces Runx2 to enhance the chondrogenic potential of MPCs

Abstract

Degeneration of knee joints during osteoarthritis often begins with meniscal lesions and regeneration of the inner, avascular meniscus does not occur. In this article, Miosge and colleagues show that cartilage tissue harvested from the inner human meniscus harbors unique meniscus progenitor cells (MPCs). These cells are controlled by canonical TGF-β signaling that leads to an increase in their chondrogenic potential.