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间充质干细胞可改变易感和抗性小鼠体内巨噬细胞对硕大利什曼原虫感染的免疫反应。

Mesenchymal stem cells alter macrophage immune responses to Leishmania major infection in both susceptible and resistance mice.

作者信息

Dameshghi Safura, Zavaran-Hosseini Ahmad, Soudi Sara, Shirazi Fatemeh Jalali, Nojehdehi Shahrzad, Hashemi Seyed Mahmoud

机构信息

Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Immunol Lett. 2016 Feb;170:15-26. doi: 10.1016/j.imlet.2015.12.002. Epub 2015 Dec 15.

Abstract

Mesenchymal stem cells (MSCs) are attracted to inflammation site and switch immune system to modulate inflammatory responses. This ability makes MSCs the best candidate cells for stem cell therapy of infection diseases. Therefore, we aimed to evaluate the modulatory effect of adipose-derived MSCs (AD-MSCs) on macrophages in Leishmania (L.) major infection. Macrophages and MSCs were isolated from both susceptible (BALB/c) and resistance (C57BL/6) strains. After co-culture of AD-MSCs with macrophages using a transwell system, we assessed MSCs-educated macrophage responses to L. major infection. Our results indicated suppression in levels of tumor necrosis factor α (TNF-α) and interleukin 10 (IL-10) of MSCs co-cultured macrophages in response to L. major infection. To clarify the effects of this suppression on inflammatory conditions, TNF-α/IL-10 ratio was calculated, indicating an increase in TNF-α/IL-10 ratio in MSCs co-cultured groups. The higher TNF-α/IL-10 ratio was observed in BALB/c macrophages co-cultured with BALB/c MSCs. Nitric oxide (NO) assay presented a significant reduction in the supernatant of all MSCs co-cultured groups compared to control. We observed a significant reduction in phagocytosis of MSCs co-cultured groups in response to L. major infection without any significant differences in the phagocytic index. In conclusion, our results represented a new spectrum of immunomodulation induced by MSCs co-cultured with macrophages in response to L. major infection. The magnitude of immunoregulation was different between BALB/c and C57BL/6 strains. Our findings also showed that MSCs exerted potential effect of M1 polarization due to unequal decrease in levels of TNF-α and IL-10 when we considered TNF-α and IL-10as representatives of M1 and M2 phenotypes, respectively. Induction of inflammatory cytokine milieu and reduction in level of IL-10 provides a new hope for stem cell therapy of leishmaniasis in susceptible models.

摘要

间充质干细胞(MSCs)被吸引至炎症部位,并调节免疫系统以调控炎症反应。这种能力使MSCs成为感染性疾病干细胞治疗的最佳候选细胞。因此,我们旨在评估脂肪来源的间充质干细胞(AD-MSCs)对杜氏利什曼原虫(L.)主要感染中巨噬细胞的调节作用。巨噬细胞和MSCs均从易感(BALB/c)和抗性(C57BL/6)品系中分离得到。使用Transwell系统将AD-MSCs与巨噬细胞共培养后,我们评估了经MSCs诱导的巨噬细胞对杜氏利什曼原虫主要感染的反应。我们的结果表明,共培养的MSCs巨噬细胞在对杜氏利什曼原虫主要感染的反应中,肿瘤坏死因子α(TNF-α)和白细胞介素10(IL-10)水平受到抑制。为阐明这种抑制对炎症状态的影响,计算了TNF-α/IL-10比值,结果表明共培养的MSCs组中TNF-α/IL-10比值升高。在与BALB/c MSCs共培养的BALB/c巨噬细胞中观察到更高的TNF-α/IL-10比值。一氧化氮(NO)检测显示,与对照组相比,所有共培养的MSCs组的上清液中NO显著减少。我们观察到共培养的MSCs组在对杜氏利什曼原虫主要感染的反应中吞噬作用显著降低,而吞噬指数无显著差异。总之,我们的结果揭示了在对杜氏利什曼原虫主要感染的反应中,与巨噬细胞共培养的MSCs诱导的免疫调节新谱。BALB/c和C57BL/6品系之间的免疫调节程度不同。我们的研究结果还表明,当我们分别将TNF-α和IL-10视为M1和M2表型的代表时,由于TNF-α和IL-10水平下降不均等,MSCs发挥了M1极化的潜在作用。炎症细胞因子环境的诱导和IL-10水平的降低为易感模型中利什曼病的干细胞治疗提供了新希望。

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