Theory-based cryopreservation mode of mesenchymal stromal cell spheroids

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-05-27 DOI:10.1016/j.cryobiol.2024.104906
O.I. Gordiyenko , I.F. Kovalenko , O.Y. Rogulska , N.A. Trufanova , T.M. Gurina , O.V. Trufanov , O.Y. Petrenko
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Abstract

Cryopreservation of spheroids requires development of new improved methods. The plasma membranes permeability coefficients for water and cryoprotectants determine time characteristics of mass transfer through the cell membranes, and therefore the optimal modes of cells cryopreservation. Here we proposed an approach to cryopreservation of multicellular spheroids which considers their generalized characteristics as analogues of the membranes’ permeability coefficients of the individual cells. We have determined such integral characteristics of spheroids from mesenchymal stromal cells (MSCs) as osmotically inactive volume; permeability coefficients for water and Me2SO molecules and the activation energy of their penetration. Based on these characteristics, we calculated the osmotic behavior of multicellular spheroids under cooling conditions to select the optimal cooling rate. We also determined the optimal cooling rate of spheroids using the probabilistic model developed based on the two-factor theory of cryodamage. From the calculation it follows that the optimal cooling rate of the MSC-based spheroids is 0.75°С/min. To verify the obtained theoretical estimates, we conducted experiments on freezing MSC-based spheroids under different modes. The obtained results of primary viability screening indicate that freezing at a constant linear cooling rate of 0.75–1.0°С/min gives a good result. Theoretical prediction of the spheroid osmotic behavior during cooling provided the basis for experimental verification of varying the temperature to which slow cooling should be carried out before immersion in liquid nitrogen. Slow freezing of spheroids to −40 °C followed by immersion in liquid nitrogen was shown to preserve cells better than slow freezing to −80 °C. Obtained data allow more effective use of MSC-based spheroids in drug screening and regenerative medicine.

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基于理论的间充质基质细胞球体冷冻保存模式。
球形细胞的冷冻保存需要开发新的改良方法。质膜对水和低温保护剂的渗透系数决定了通过细胞膜传质的时间特性,因此也决定了细胞低温保存的最佳模式。在此,我们提出了一种低温保存多细胞球的方法,该方法将多细胞球的总体特征视为单个细胞膜渗透系数的类似物。我们已经确定了间充质基质细胞(MSCs)球体的整体特征,如无渗透性体积、水和 Me2SO 分子的渗透系数及其渗透活化能。根据这些特征,我们计算了多细胞球体在冷却条件下的渗透行为,以选择最佳冷却速率。我们还利用基于低温损伤双因素理论开发的概率模型确定了球形体的最佳冷却速率。根据计算结果,基于 MSC 的球体的最佳冷却速率为 0.75 °С/分钟。为了验证所获得的理论估计值,我们进行了基于间充质干细胞的球体在不同模式下的冷冻实验。初步活力筛选结果表明,以 0.75 - 1.0 °С/min 的恒定线性冷却速率冷冻效果良好。对冷却过程中球体渗透行为的理论预测为实验验证提供了依据,实验验证了在浸入液氮前应改变缓慢冷却的温度。结果表明,将球形细胞缓慢冷冻至-40 °C,然后浸入液氮比缓慢冷冻至-80 °C更能保存细胞。所获得的数据有助于在药物筛选和再生医学中更有效地利用基于间充质干细胞的球形细胞。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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