Skip to main content

ORIGINAL RESEARCH article

Front. Vet. Sci.
Sec. Veterinary Regenerative Medicine
Volume 11 - 2024 | doi: 10.3389/fvets.2024.1410855
This article is part of the Research Topic Links Between Regenerative Medicine and Immunotherapy: How Cellular Therapies Modulate Immune Responses for Improved Outcomes View all 7 articles

Impact of different formulations of platelet lysate on proliferative and immune profile of equine mesenchymal stromal cells

Provisionally accepted
Kevin Yaneselli Kevin Yaneselli 1*Gimena Ávila Gimena Ávila 1Andrea Rossi Andrea Rossi 2Analía Rial Analía Rial 2Sabrina Castro Sabrina Castro 1María J. Estradé María J. Estradé 1Agustina Algorta Agustina Algorta 1
  • 1 Faculty of Veterinary Medicine, University of the Republic, Montevideo, Uruguay
  • 2 Department of Biotechnological Development, Faculty of Medicine, University of the Republic, Montevideo, Uruguay

The final, formatted version of the article will be published soon.

    Platelet lysate (PL) is investigated as a potential replacement for fetal bovine serum (FBS) in cell culture. However, there is limited research on its impact on the immune profile of equine mesenchymal stromal cells (eMSCs). This study aimed to evaluate the effects of different PL formulations on the proliferative capacity, multipotentiality, and immune profile of equine adipose tissue-derived MSCs (eAD-MSCs). In vitro growth kinetics and trilineage differentiation of eAD-MSCs (n = 7) were assessed under three culture conditions: medium-concentration PL (MPL), highconcentration PL (HPL), and FBS as a control. The immune profile was evaluated by studying the expression of immunogenic receptors such as MHC I, MHC II, and immunomodulatory molecules IL-6, IL-10, and TNF-α, determined by gene expression, surface marker expression, and cytokine quantification. Both PL formulations, pooled from 5 donors, exhibited 3.3 and 6.5-fold higher platelet counts than baseline plasma for MPL and HPL, respectively. Higher concentrations of TGF-β and PDGF were found in both PL formulations compared to baseline. Furthermore, MPL and HPL subcultures demonstrated proliferative, clonogenic, and multipotent capacities similar to FBS. The immune profile of PL-cultured cells exhibited gene expression levels related to immunogenicity and immunomodulation similar to the reference condition, and the surface antigen presence of MHC II was also similar. However, HPL media exhibited higher IL-6, IL-10, and TNF-α concentrations in the culture supernatant. In conclusion, both PL media contained higher concentrations of growth factors compared to FBS, supporting the in vitro culture of eAD-MSCs with proliferative, clonogenic, and multipotent capacity similar to the reference medium. Nonetheless, PL usage led to a variation in the immunomodulatory cytokine microenvironment, with higher concentrations of IL-6, IL-10, and TNF-α in HPL media compared to MPL and FBS.

    Keywords: Platelet lysate, horse, Mesenchymal stromal/stem cells, Fetal bovine serum, xeno-free media, immunology

    Received: 01 Apr 2024; Accepted: 01 Jul 2024.

    Copyright: © 2024 Yaneselli, Ávila, Rossi, Rial, Castro, Estradé and Algorta. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Kevin Yaneselli, Faculty of Veterinary Medicine, University of the Republic, Montevideo, Uruguay

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.