Harnessing matrix stiffness to engineer a bone marrow niche for hematopoietic stem cell rejuvenation

Cell Stem Cell. 2023 Apr 6;30(4):378-395.e8. doi: 10.1016/j.stem.2023.03.005.

Abstract

Hematopoietic stem cell (HSC) self-renewal and aging are tightly regulated by paracrine factors from the bone marrow niche. However, whether HSC rejuvenation could be achieved by engineering a bone marrow niche ex vivo remains unknown. Here, we show that matrix stiffness fine-tunes HSC niche factor expression by bone marrow stromal cells (BMSCs). Increased stiffness activates Yap/Taz signaling to promote BMSC expansion upon 2D culture, which is largely reversed by 3D culture in soft gelatin methacrylate hydrogels. Notably, 3D co-culture with BMSCs promotes HSC maintenance and lymphopoiesis, reverses aging hallmarks of HSCs, and restores their long-term multilineage reconstitution capacity. In situ atomic force microscopy analysis reveals that mouse bone marrow stiffens with age, which correlates with a compromised HSC niche. Taken together, this study highlights the biomechanical regulation of the HSC niche by BMSCs, which could be harnessed to engineer a soft bone marrow niche for HSC rejuvenation.

Keywords: aging; bone marrow stromal cell; hematopoietic stem cell; matrix; niche; rejuvenation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow* / metabolism
  • Coculture Techniques
  • Hematopoietic Stem Cells / metabolism
  • Mesenchymal Stem Cells* / metabolism
  • Mice
  • Rejuvenation
  • Stem Cell Niche