Intraarticular senescent chondrocytes impair the cartilage regeneration capacity of mesenchymal stem cells

Stem Cell Res Ther. 2019 Mar 12;10(1):86. doi: 10.1186/s13287-019-1193-1.

Abstract

Background: Senescent cells exert a significant influence over their surrounding cellular environment. Senescent chondrocytes (SnChos) were found to be accumulated in degenerated cartilage present in joints affected by osteoarthritis. The influence of SnChos on exogenously transplanted stem cells has yet to be reported.

Methods: In this study, we evaluated the interactions between SnChos and bone marrow mesenchymal stem cells (BMSCs) when co-cultured as well as in the intra-articular senescent microenvironment (IASM). The effect of IASM on cartilage regeneration was also assessed.

Results: It was found that a small fraction of SnChos induced BMSC cellular senescence and apoptosis. SnChos also inhibited proliferation, facilitated stemness, and suppressed chondrogenic differentiation of BMSCs. BMSCs induced the apoptosis of SnChos, reduced the proportion of SnChos, stimulated SnChos proliferation, and revealed a bidirectional effect on SnChos inflammaging. IASM significantly suppressed the survival, proliferation, and appropriate differentiation of grafted BMSCs in vivo, all of which impaired cartilage regeneration. Anti-senescence agent ABT-263 was able to partly rescue the cells from the negative effects of SnChos.

Conclusions: The SnChos and BMSCs interacted with each other at cellular senescence, apoptosis, proliferation, differentiation, and cell functions. This interaction impaired the cartilage repair of MSCs. Anti-senescence agent provided a possible solution for this impairment.

Keywords: Bone marrow mesenchymal stem cells (BMSCs); Cartilage repair; Intra-articular senescent microenvironment (IASM); Osteoarthritis (OA); Senescent chondrocytes (SnChos).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage / pathology
  • Cartilage / physiology*
  • Cellular Senescence*
  • Chondrocytes / metabolism*
  • Chondrocytes / pathology
  • Coculture Techniques
  • Male
  • Mesenchymal Stem Cells / metabolism*
  • Mesenchymal Stem Cells / pathology
  • Rats
  • Rats, Sprague-Dawley
  • Regeneration*