Effect of Expansion Media on Functional Characteristics of Bone Marrow-Derived Mesenchymal Stromal Cells

Author:

Jakl Viktoria1,Popp Tanja2ORCID,Haupt Julian23,Port Matthias2,Roesler Reinhild4,Wiese Sebastian4ORCID,Friemert Benedikt3,Rojewski Markus T.15ORCID,Schrezenmeier Hubert15

Affiliation:

1. Institute for Transfusion Medicine, University Hospital Ulm, 89081 Ulm, Germany

2. Bundeswehr Institute of Radiobiology, 80937 Munich, Germany

3. Clinic for Trauma Surgery and Orthopedics, Army Hospital Ulm, 89081 Ulm, Germany

4. Core Unit of Mass Spectrometry and Proteomics, Ulm University Medical Center, 89081 Ulm, Germany

5. Institute for Clinical Transfusion Medicine and Immunogenetics Ulm, German Red Cross Blood Donation Service Baden-Württemberg—Hessia and University Hospital Ulm, 89081 Ulm, Germany

Abstract

The therapeutic efficacy of mesenchymal stromal cells (MSCs) has been shown to rely on their immunomodulatory and regenerative properties. In order to obtain sufficient numbers of cells for clinical applications, MSCs have to be expanded ex vivo. Expansion media with xenogeneic-free (XF) growth-promoting supplements like human platelet lysate (PL) or serum- and xenogeneic-free (SF/XF) formulations have been established as safe and efficient, and both groups provide different beneficial qualities. In this study, MSCs were expanded in XF or SF/XF media as well as in mixtures thereof. MSCs cultured in these media were analyzed for phenotypic and functional properties. MSC expansion was optimal with SF/XF conditions when PL was present. Metabolic patterns, consumption of growth factors, and secretome of MSCs differed depending on the type and concentration of supplement. The lactate per glucose yield increased along with a higher proportion of PL. Many factors in the supernatant of cultured MSCs showed distinct patterns depending on the supplement (e.g., FGF-2, TGFβ, and insulin only in PL-expanded MSC, and leptin, sCD40L PDGF-AA only in SF/XF-expanded MSC). This also resulted in changes in cell characteristics like migratory potential. These findings support current approaches where growth media may be utilized for priming MSCs for specific therapeutic applications.

Funder

Sanitätsakademie der Bundeswehr

University of Ulm

Publisher

MDPI AG

Subject

General Medicine

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