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Modulation of the mesenchymal stem cell migration capacity via preconditioning with topographic microstructure
Zhengdong Li1,2, Xun Xu1,2, Weiwei Wang1
1Institute of Biomaterial Science and Berlin-Brandenburg Center for Regenerative Therapies, Helmholtz-Zentrum Geesthacht, Teltow, Germany.
Clinical Hemorheology and Microcirculation
|September 5, 2017
Summary
Microscale roughness on culture surfaces enhances mesenchymal stem cells (MSCs) migration velocity. This physical preconditioning strategy also boosts focal adhesion kinase (FAK) and mitogen-activated protein kinase (MAPK) activation for improved therapeutic potential.
Area of Science:
- Biomaterials Science
- Stem Cell Biology
- Regenerative Medicine
Background:
- Mesenchymal stem cells (MSCs) possess significant therapeutic potential, but controlling their behavior, particularly migration, is crucial for effective application.
- Current methods to influence MSC migration are diverse, yet efficient physical preconditioning strategies are continuously sought.
- Understanding the cellular mechanisms underlying MSC migration modulation is key to advancing regenerative medicine.
Purpose of the Study:
- To investigate the impact of topographic microstructures on polystyrene (PS) culture surfaces as a physical preconditioning method for modulating MSC migration.
- To assess the effect of microscale roughness on the mobilization velocity and migratory behavior of human adipose-derived mesenchymal stem cells (hADSCs).
- To examine the involvement of key signaling pathways, specifically focal adhesion kinase (FAK) and mitogen-activated protein kinase (MAPK), in microtopography-induced MSC responses.
Main Methods:
- Creation of polystyrene culture vessel surfaces with varying topographic microstructures at the microscale.
- Preconditioning of human adipose-derived mesenchymal stem cells (hADSCs) on these engineered surfaces.
- Analysis of cell migration trajectories after reseeding to quantify mobilization velocity.
- Biochemical assays to measure the activation levels of focal adhesion kinase (FAK) and mitogen-activated protein kinase (MAPK).
Main Results:
- Brief preconditioning with specific microtopographies significantly promoted the mobilization velocity of hADSCs.
- The enhanced migration velocity persisted even after the removal of the microstructured surface.
- Elevated activation levels of FAK and MAPK were observed in hADSCs during and following the microtopography preconditioning.
Conclusions:
- Topographic microstructures on culture surfaces offer a feasible physical strategy to enhance MSC migration.
- This preconditioning approach effectively modulates hADSC mobilization velocity and key intracellular signaling pathways (FAK, MAPK).
- Transplantation of stem cells preconditioned with microtopography holds promise for enhancing therapeutic efficacy in regenerative medicine applications.

