1 Department of Urology, Osaka University Graduate School of Medicine, Osaka, Japan. 2 Department of Gastroenterological Surgery, National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Hiroshima, Japan. 3 Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine, Osaka, Japan. 4 Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Osaka, Japan. 5 Address correspondence to: Masayoshi Okumi, M.D., Ph.D., Department of Urology, Osaka University Graduate School of Medicine, 2-2 E4 Yamadaoka, Suita, Osaka 565-0871, Japan; Masahiro Tanemura, M.D., Ph.D., Department of Gastroenterological Surgery, National Hospital Organization Kure Medical Center and Chugoku Cancer Center, 3-1 Aoyamacho, Kure, Hiroshima 737-0023, Japan.
Transplantation. 2014 Aug 15;98(3):277-84. doi: 10.1097/TP.0000000000000230.
In addition to its abundance and easy accessibility, adipose tissue yields more potent immunoregulatory stem cells (adipose tissue-derived stem cells, ADSCs) than does bone marrow. However, the beneficial effects of ADSCs on alloreactivity are scarcely known. This study evaluated the beneficial effects of ADSCs in rat kidney transplantation and analyzed the underlying molecular mechanism.
Dark Agouti rat kidneys were transplanted into Lewis rats. Autologous ADSCs (2×10) were injected through the left renal artery of the donors before the nephrectomy (ADSCs group). Graft survival, histologic changes, and the expression of several cytokines and proteins were assessed. In an in vitro experiment, the immunosuppressive capacity of ADSCs was tested in a mixed lymphocyte reaction.
Histologic findings of the ADSCs group revealed a reduced rejection grade, whereas the number of infiltrated CD4/CD8 T cells was also significantly decreased as compared to the control. Relative to these findings, injection of ADSCs led to a significantly prolonged mean graft survival compared with the control. In vitro, autologous ADSCs dose-dependently suppressed alloreactive lymphocytes. Moreover, ADSCs increased the level of tumor necrosis factor-inducible gene 6 protein (TSG-6) in mixed lymphocyte reaction, which has an anti-inflammatory capacity. Recombinant TSG-6 markedly suppressed alloreactive T cells through downregulating CD44, which may lead to the suppression of T-cell activation and infiltration into allografts.
Our findings clearly showed that ADSCs attenuated acute rejection by secreting TSG-6 as well as through direct cell interaction. These findings contribute to the clinical application of these cells in solid organ transplantation.
脂肪组织不仅丰富且易于获取,还能产生比骨髓更有效的免疫调节干细胞(脂肪组织源性干细胞,ADSCs)。然而,ADSCs 对同种异体反应的有益影响鲜为人知。本研究评估了 ADSCs 在大鼠肾移植中的有益作用,并分析了其潜在的分子机制。
将黑毛 Agouti 大鼠的肾脏移植到 Lewis 大鼠体内。在供体肾切除前,通过左肾动脉注射 2×10 个自体 ADSCs(ADSCs 组)。评估移植物存活、组织学变化以及几种细胞因子和蛋白的表达。在体外实验中,通过混合淋巴细胞反应测试 ADSCs 的免疫抑制能力。
ADSCs 组的组织学发现表明排斥反应程度降低,与对照组相比,浸润的 CD4/CD8 T 细胞数量也明显减少。与这些发现相比,与对照组相比,ADSCs 注射导致平均移植物存活时间显著延长。在体外,自体 ADSCs 呈剂量依赖性抑制同种反应性淋巴细胞。此外,ADSCs 在混合淋巴细胞反应中增加肿瘤坏死因子诱导基因 6 蛋白(TSG-6)的水平,具有抗炎能力。重组 TSG-6 通过下调 CD44 显著抑制同种反应性 T 细胞,这可能导致 T 细胞活化和浸润同种移植物的抑制。
我们的研究结果清楚地表明,ADSCs 通过分泌 TSG-6 以及通过直接细胞相互作用来减轻急性排斥反应。这些发现为这些细胞在实体器官移植中的临床应用提供了依据。