Budesonide Analogues Preserve Stem Cell Pluripotency and Delay 3D Gastruloid Development

Author:

Amoroso Filomena12ORCID,Ibello Eduardo12ORCID,Saracino Federica1,Cermola Federica1,Ponticelli Giovanna1ORCID,Scalera Enrica3ORCID,Ricci Francesca3,Villetti Gino3,Cobellis Gilda2ORCID,Minchiotti Gabriella1ORCID,Patriarca Eduardo Jorge1,De Cesare Dario1,D’Aniello Cristina1

Affiliation:

1. Stem Cell Fate Laboratory, Institute of Genetics and Biophysics “A. Buzzati Traverso”, Consiglio Nazionale delle Ricerche (CNR), 80131 Naples, Italy

2. Department of Precision Medicine, University of Campania Luigi Vanvitelli, 80138 Naples, Italy

3. Experimental Pharmacology & Translational Science Department, Corporate Pre-Clinical R&D, Chiesi Farmaceutici S.p.A., 43122 Parma, Italy

Abstract

Small molecules that can modulate or stabilize cell–cell interactions are valuable tools for investigating the impact of collective cell behavior on various biological processes such as development/morphogenesis, tissue regeneration and cancer progression. Recently, we showed that budesonide, a glucocorticoid widely used as an anti-asthmatic drug, is a potent regulator of stem cell pluripotency. Here we tested the effect of different budesonide derivatives and identified CHD-030498 as a more effective analogue of budesonide. CHD-030498 was able to prevent stem cell pluripotency exit in different cell-based models, including embryonic stem-to-mesenchymal transition, spontaneous differentiation and 3D gastruloid development, and at lower doses compared to budesonide.

Publisher

MDPI AG

Subject

Pharmaceutical Science

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