Tuning Secretomes for Regenerative Medicine

In this narrative review, the systematic tailoring of cell-derived secretomes for regenerative medicine is comprehensively discussed. The review begins by evaluating a diverse array of cell sources, including platelets, endothelial cells, osteoblasts, chondrocytes, tenocytes, and mesenchymal stem cells (MSCs). From this foundation, we critically analyze how modulating cell culture conditions can be used to directly influence the therapeutic and paracrine profiles of the resulting secretomes. Specifically, we address the impact of the following critical parameters on secretome fabrication: (i) Culture Medium Supplementation: The use of defined media, supplements, and chemical priming agents. (ii) Cell Cultivation Formats: A comparative analysis of 2D monolayer cultures versus 3D spheroids. (iii) Culture Duration and Fluidics: The effects of culture time alongside static versus dynamic culture systems. (iv) Microenvironmental Stress: The influence of varying oxygen levels (for example, hypoxia) and induced oxidative stress on secretory output.

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Publication Details

Journal
Biology
Published
2026-06-16
DOI
https://doi.org/10.3390/biology15120941
Primary Topic
Periodontal Regeneration and Treatments
Type
article
Field-Weighted Citation Impact
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article

Tuning Secretomes for Regenerative Medicine

Johanna Buschmann
Biology
Periodontal Regeneration and Treatments
article

Tuning Secretomes for Regenerative Medicine

Johanna Buschmann
article en

Abstract

In this narrative review, the systematic tailoring of cell-derived secretomes for regenerative medicine is comprehensively discussed. The review begins by evaluating a diverse array of cell sources, including platelets, endothelial cells, osteoblasts, chondrocytes, tenocytes, and mesenchymal stem cells (MSCs). From this foundation, we critically analyze how modulating cell culture conditions can be used to directly influence the therapeutic and paracrine profiles of the resulting secretomes. Specifically, we address the impact of the following critical parameters on secretome fabrication: (i) Culture Medium Supplementation: The use of defined media, supplements, and chemical priming agents. (ii) Cell Cultivation Formats: A comparative analysis of 2D monolayer cultures versus 3D spheroids. (iii) Culture Duration and Fluidics: The effects of culture time alongside static versus dynamic culture systems. (iv) Microenvironmental Stress: The influence of varying oxygen levels (for example, hypoxia) and induced oxidative stress on secretory output.

BiologyVol. 15(12)
University Hospital of Zurich (CH)
Openalex Percentile: Top 5%
Periodontal Regeneration and Treatments
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