Microtissues®

Summary

Published in Frontiers in Bioengineering and Biotechnology (2023), this peer-reviewed study used 3D Petri Dish® micro-molds to form scaffold-free 3D microtissues. Full citation: Rovere, Matteo, et al. Spheroid size influences cellular senescence and angiogenic potential of mesenchymal stromal cell-derived soluble factors and extracellular vesicles

🔬 Stem Cells

Spheroid size influences cellular senescence and angiogenic potential of mesenchymal stromal cell-derived soluble factors and extracellular vesicles

Frontiers in Bioengineering and Biotechnology 2023 Rovere, Matteo, et al
Cite as: Rovere, Matteo, et al. Spheroid size influences cellular senescence and angiogenic potential of mesenchymal stromal cell-derived soluble factors and extracellular vesicles. Frontiers in Bioengineering and Biotechnology (2023). doi:10.3389/fbioe.2023.1297644 doi.org/10.3389/fbioe.2023.1297644

Research Overview

The mesenchymal stromal cell secretome is an emerging regenerative tool, and 3D culture preserves MSC phenotype during extended maintenance. The spheroid interior, however, is hypoxic — which may boost the angiogenic output of adult MSCs, whose angiogenic potential normally trails that of perinatal-tissue MSCs.

This study compared large spheroids (2,600 cells, ~300 µm) with small ones (1,000 cells, ~200 µm) to determine how spheroid size shapes cellular senescence and angiogenic potential, isolating size — and the internal hypoxia that comes with it — as a controllable variable in secretome production.

Key Discoveries

  • Large (~300 µm, 2,600 cells) and small (~200 µm, 1,000 cells) MSC spheroids compared directly
  • Spheroid size tested as a driver of senescence and angiogenic secretome output
  • Internal hypoxia proposed as the mechanism boosting adult MSC angiogenic potential