Mita A, Ricordi C, Miki A, Barker S, Khan A, Alvarez A, Hashikura Y, Miyagawa S, Ichii H
Cell Transplant Center, Diabetes Research Institute, University of Miami Leonard M. Miller School of Medicine, Miami, Florida 33136, USA.
Transplant Proc. 2009 Jan-Feb;41(1):314-5. doi: 10.1016/j.transproceed.2008.10.059.
Purification is one of the most important steps in human islet isolation. Although Ficoll-based density gradients are widely used, OptiPrep-based density gradients are used in few centers. Cytokine/chemokine production from human islet preparations varies widely. Some cytokines/chemokines have been reported to have adverse effects on human islet preparations. Control of cytokine/chemokine production may be a key to improve islet quality and quantity, leading to better transplantation outcomes. The aim of the present study was to investigate the effects on islet preparations of purification methods using various density gradients on viability, cellular composition, and proinflammatory cytokine/chemokine production. After the digestion phase, the extracts were divided into 2 groups for purification using a semiautomated cell processor with Ficoll-based or OptiPrep-based density gradients. Islet preparations cultured for 2 days were assessed regarding islet cell viability (fluorescein diacetate/propidium iodide [FDA/PI]), fractional beta-cell viability by FACS, and beta-cell content using iCys. Cytokine/chemokine production from islet preparations was also measured by Bio-plex. After purification, the purity, islet equivalents (IEQ), and islet recovery rates were comparable between the 2 groups. Although FDA/PI and fractional beta-cell viability showed no significant difference, survival of beta cells during culture was significantly higher in the OptiPrep compared with the Ficoll-based density gradient group. There were significantly lower tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, interferon (IFN)-gamma, IL-6, and MIP-1beta productions from the OptiPrep-based density gradient group. OptiPrep-based density gradients reduced cytokine/chemokine production by islet preparations. In addition, OptiPrep-based density gradient purification significantly reduced the loss of beta-cell mass during pretransplantation culture.
纯化是人类胰岛分离过程中最重要的步骤之一。尽管基于Ficoll的密度梯度法被广泛应用,但基于OptiPrep的密度梯度法仅在少数中心使用。人胰岛制剂中细胞因子/趋化因子的产生差异很大。据报道,一些细胞因子/趋化因子对人胰岛制剂有不良影响。控制细胞因子/趋化因子的产生可能是提高胰岛质量和数量的关键,从而带来更好的移植效果。本研究的目的是探讨使用各种密度梯度的纯化方法对胰岛制剂的活力、细胞组成以及促炎细胞因子/趋化因子产生的影响。消化阶段后,提取物被分为两组,使用基于Ficoll或OptiPrep密度梯度的半自动细胞处理器进行纯化。对培养2天的胰岛制剂进行评估,包括胰岛细胞活力(荧光素二乙酸酯/碘化丙啶[FDA/PI])、通过流式细胞术检测的β细胞活力分数以及使用iCys检测的β细胞含量。胰岛制剂中细胞因子/趋化因子的产生也通过Bio-plex进行测量。纯化后,两组之间的纯度、胰岛当量(IEQ)和胰岛回收率相当。尽管FDA/PI和β细胞活力分数没有显著差异,但与基于Ficoll的密度梯度组相比,OptiPrep组在培养期间β细胞的存活率显著更高。基于OptiPrep的密度梯度组中肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、干扰素(IFN)-γ、IL-6和MIP-1β的产生显著更低。基于OptiPrep的密度梯度降低了胰岛制剂中细胞因子/趋化因子的产生。此外,基于OptiPrep的密度梯度纯化显著减少了移植前培养期间β细胞质量的损失。