Molecular and Cellular Analysis of Lipogems-Processed Lipoaspirates for Evaluating the Efficacy of Treatments in Regenerative Medicine
Autologous adipose tissue is a readily available source of mesenchymal stromal cells (MSCs) for regenerative applications. Here, human lipoaspirates from eight donors processed with the Lipogems system were characterized by flow cytometry (MSC/pericyte markers and inflammatory markers), immunocytochemistry (NANOG, OCT3/4, SOX2), and functional assays assessing proliferation, senescence, apoptosis, multilineage differentiation, IDO activity, and ROS levels. Lipogems-derived cultures fulfilled MSC immunophenotypic criteria while showing marked inter-donor variability in MSC/pericyte proportions, stemness-marker expression, differentiation bias, inflammatory profile, and oxidative status. In contrast, senescence and apoptosis were comparable across samples. Clinical evaluation, based on surgeon-assessed outcomes after autologous treatment, scored on a 1–10 scale, was consistently high across donors (7–10). Overall, Lipogems-processed lipoaspirates harbor a heterogeneous but functionally competent stromal compartment; these data support a sample-specific quality framework (composition, differentiation tendency, inflammation/ROS, IDO responsiveness) to improve reproducibility and optimization of regenerative protocols.
Authors
- Beatrice Castiglioni
- Michela Bosetti (ORCID: https://orcid.org/0000-0002-3682-8702)
- Domenico Aprile (ORCID: https://orcid.org/0000-0003-1166-3259)
- Tiziana Squillaro (ORCID: https://orcid.org/0000-0003-1088-5351)
- G. Di Bernardo
- N. Alessio
- Sura H. A. Al Sammarraie
Institutions
- Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT)
- University of Campania "Luigi Vanvitelli" (IT)
- Link Campus University (IT)
- Temple University (US)
Publication Details
- Journal
- Stem Cell Reviews and Reports
- Published
- 2026-04-11
- DOI
- https://doi.org/10.1007/s12015-026-11094-9
- Primary Topic
- Mesenchymal stem cell research
- Type
- article
- Field-Weighted Citation Impact
- 0.00