Maia Leandro, Dias Marianne Camargos, de Moraes Carolina Nogueira, de Paula Freitas-Dell'Aqua Camila, da Mota Ligia S L Silveira, Santiloni Valquíria, da Cruz Landim-Alvarenga Fernanda
Department of Animal Reproduction, São Paulo State University, Prof. Doutor Walter Mauricio Correa n/n, CEP: 18618-681, Botucatu, São Paulo, Brazil.
Department of Genetics, Bioscience Institute, São Paulo State University, Prof. Dr. Antônio Celso Wagner Zanin, 250, CEP: 18618-689, Botucatu, São Paulo, Brazil.
Cell Biol Int. 2017 Mar;41(3):239-248. doi: 10.1002/cbin.10708. Epub 2017 Feb 2.
Cryopreservation is a feasible alternative to maintaining several cell lines, particularly for immediate therapeutic use, transportation of samples, and implementation of new in vitro studies. This work parts from the hypothesis that the medium of cryopreservation composed by 90% of conditioned medium (CM) supports cryopreservation of equine umbilical cord intervascular matrix mesenchymal stem cells (UCIM-MSCs), allowing the maintenance of the biological properties for the establishment of cell banks intended for therapeutic use and in vitro studies. Thus, we evaluated the viability, apoptosis/necrosis rates, immunophenotypic profile (IP), chromosomal stability, clonicity, and differentiation potential of UCIM-MSCs cryopreserved with four different mediums (with FBS: M1, M3, M4 and without FBS: M2). After 3 months of cryopreservation, samples were thawed and analyzed. The potential of differentiation in the mesodermal lineages, clonicity, and the chromosomal stability were maintained after cryopreservation of UCIM-MSCs with medium containing FBS. Changes (P < 0.05) at IP for some markers were observed at cells cryopreserved with medium M1-M3. Only the UCIM-MSCs cryopreserved with the CM (M4) had similar viability post-thaw (P = 0.23) when compared with fresh cells. We proved the hypothesis that the medium of cryopreservation containing CM supports the cryopreservation of UCIM-MSCs, at the experimental conditions, being the medium that better maintains the biological characteristics observed at fresh cells. Thus, future studies of UCIM-MSCs secretome should be conducted to better understand the beneficial and protective effects of the CM during the freezing process.
冷冻保存是维持多种细胞系的一种可行替代方法,特别是对于即时治疗用途、样本运输以及开展新的体外研究而言。本研究基于这样的假设:由90%的条件培养基(CM)组成的冷冻保存培养基能够支持马脐带血管间充质干细胞(UCIM-MSCs)的冷冻保存,从而维持其生物学特性,以建立用于治疗和体外研究的细胞库。因此,我们评估了用四种不同培养基(含胎牛血清:M1、M3、M4;不含胎牛血清:M2)冷冻保存的UCIM-MSCs的活力、凋亡/坏死率、免疫表型谱(IP)、染色体稳定性、克隆性和分化潜能。冷冻保存3个月后,将样本解冻并进行分析。用含胎牛血清的培养基冷冻保存UCIM-MSCs后,其在中胚层谱系中的分化潜能、克隆性和染色体稳定性得以维持。在用M1 - M3培养基冷冻保存的细胞中,观察到某些标志物的IP发生了变化(P < 0.05)。与新鲜细胞相比,只有用CM(M4)冷冻保存的UCIM-MSCs解冻后的活力相似(P = 0.23)。我们证实了这一假设:在实验条件下,含CM的冷冻保存培养基能够支持UCIM-MSCs的冷冻保存,该培养基能更好地维持新鲜细胞所观察到的生物学特性。因此,未来应开展UCIM-MSCs分泌组的研究,以更好地了解CM在冷冻过程中的有益和保护作用。