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多次系统性给予间充质干细胞条件培养基可作为“魔法子弹”,恢复哮喘大鼠 IFN-γ/IL-4 平衡。

Systemic delivery of mesenchymal stem cells condition media in repeated doses acts as magic bullets in restoring IFN-γ/IL-4 balance in asthmatic rats.

机构信息

Drug Applied Research Center, Tabriz University of medical sciences, Tabriz, Iran.

Drug Applied Research Center, Tabriz University of medical sciences, Tabriz, Iran; Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Applied Cell Sciences, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Life Sci. 2018 Nov 1;212:30-36. doi: 10.1016/j.lfs.2018.09.049. Epub 2018 Sep 27.

Abstract

AIMS

With respect to recent advantage in stem cell application, given the concern reported previously after stem cell transplantation, mesenchymal stem cell-derived conditioned media (MSC-CM) could be a potential approach to guarantee more safety and efficient outcomes than the current stem cell-based regenerative therapies.

MAIN METHODS

Male rats were assigned into four experimental groups (n = 6); healthy rats (C group), OVA sensitized rats (S group), OVA sensitized rats received a single dose of 50 μl CM intravenously (S group + SD-CM) and OVA sensitized rats received repeated doses of 50 μl CM intravenously (S group + RD-CM). Two weeks post-allergen challenge, the therapeutic effects of systemic administrated CM in single and repeated dosages were investigated by monitoring the transcription of T-bet, GATA-3, IL-4 and IFN-γ genes along with pathological changes in asthmatic lung tissue. IL-4 and IFN-γ levels and IFN-γ/IL-4 ratio were further evaluated in sera.

KEY FINDINGS

Our data revealed that the systemic introduction of CM in repeated dosages could significantly reduce pathological injures in OVA-sensitized rats by the modulation of expression of T-bet and GATA-3 in lung tissues and interleukins levels (p < 0.001 to p < 0.05). In contrary, CM in single dosage did not yield any beneficial effect.

SIGNIFICANCE

Overall, we indicated that systemic administration of CM in repeated dosages, but not in single dose, could be strategic approach in amelioration of asthmatic changes, presumably by the regulating the differentiation of naive CD4 T cells into Th1/Th2 effector cells via modulation of T-bet and GATA-3 expression in OVA-sensitized male rats.

摘要

目的

鉴于最近干细胞应用的优势,间充质干细胞衍生的条件培养基(MSC-CM)可能是一种比当前基于干细胞的再生疗法更安全、更有效的方法,因为此前有报道称干细胞移植后存在担忧。

主要方法

雄性大鼠被分为四组实验(n=6);健康大鼠(C 组)、OVA 致敏大鼠(S 组)、OVA 致敏大鼠单次静脉注射 50 μl CM(S 组+SD-CM)和 OVA 致敏大鼠重复静脉注射 50 μl CM(S 组+RD-CM)。在过敏原攻击后 2 周,通过监测 T-bet、GATA-3、IL-4 和 IFN-γ 基因的转录以及哮喘肺组织的病理变化,研究单次和重复剂量系统给予 CM 的治疗效果。进一步评估血清中 IL-4 和 IFN-γ 水平和 IFN-γ/IL-4 比值。

主要发现

我们的数据表明,重复剂量的 CM 全身给药可以通过调节肺组织中 T-bet 和 GATA-3 的表达以及细胞因子水平(p<0.001 至 p<0.05)显著减轻 OVA 致敏大鼠的病理损伤。相反,单次剂量的 CM 没有产生任何有益的效果。

意义

总的来说,我们表明,重复剂量而不是单次剂量的 CM 全身给药可能是一种改善哮喘变化的策略方法,可能通过调节 T-bet 和 GATA-3 的表达来调节幼稚 CD4 T 细胞向 Th1/Th2 效应细胞的分化,从而改善 OVA 致敏雄性大鼠的哮喘变化。

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