Institute of Translational Medicine, The First Hospital of Jilin University, Changchun, 130061, China.
Department of Pediatric Gastroenterology, The First Hospital of Jilin University, Changchun, China.
Stem Cell Rev Rep. 2022 Oct;18(7):2444-2457. doi: 10.1007/s12015-022-10353-9. Epub 2022 Mar 10.
Mesenchymal stem cells (MSCs) have been used to achieve exciting therapeutic outcomes in many animal studies and clinical trials for various autoimmune diseases, including inflammatory bowel disease (IBD). Type 1 regulatory T (Tr1) cells are the main source of interleukin (IL) 10 in the intestine. Whether Tr1 cells are involved during MSC-mediated IBD treatment is unclear. We treated a murine model of 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis with human umbilical cord-derived MSCs (hUCMSCs) and found that the disease severity was alleviated significantly in a dose-dependent manner. hUCMSCs increased the proportion of Tr1 cells and decreased that of T helper (Th)-1 and Th17 cells in the spleen and mesenteric lymph nodes in different stages of colitis. We found that the upregulation of Tr1 cells by hUCMSCs was abrogated after blocking indoleamine-2,3-dioxygenase (IDO), and IDO knockdown in hUCMSCs reversed the increase in Tr1 cell proportions caused by hUCMSCs in colitis. Moreover, hUCMSCs inhibited apoptosis and promoted the proliferation of Tr1 cells. Our results suggest that Tr1 cells play an important role in the amelioration of IBD by MSCs, and they are the target population for the alleviation of IBD by MSCs, providing meaningful references for the study of therapeutic mechanisms of MSCs in other inflammatory diseases.
间充质干细胞(MSCs)已被用于实现许多动物研究和临床试验中各种自身免疫性疾病的令人兴奋的治疗结果,包括炎症性肠病(IBD)。1 型调节性 T(Tr1)细胞是肠道中白细胞介素(IL)10 的主要来源。在 MSC 介导的 IBD 治疗中是否涉及 Tr1 细胞尚不清楚。我们用人脐带来源的间充质干细胞(hUCMSCs)治疗 2,4,6-三硝基苯磺酸(TNBS)诱导的结肠炎小鼠模型,发现疾病严重程度呈剂量依赖性显著缓解。hUCMSCs 增加了脾脏和肠系膜淋巴结中 Tr1 细胞的比例,并降低了结肠炎不同阶段 Th1 和 Th17 细胞的比例。我们发现,阻断吲哚胺 2,3-双加氧酶(IDO)后,hUCMSCs 对 Tr1 细胞的上调作用被阻断,而 hUCMSCs 中的 IDO 敲低逆转了 hUCMSCs 在结肠炎中引起的 Tr1 细胞比例增加。此外,hUCMSCs 抑制了 Tr1 细胞的凋亡并促进了其增殖。我们的结果表明,Tr1 细胞在 MSC 改善 IBD 中发挥重要作用,它们是 MSC 缓解 IBD 的靶细胞群,为研究 MSC 在其他炎症性疾病中的治疗机制提供了有意义的参考。