Student Research Committee, Iran University of Medical Sciences, Tehran, Iran.
Physiology Research Centre, Iran University of Medical Sciences, Tehran, Iran.
Exp Physiol. 2021 Feb;106(2):544-554. doi: 10.1113/EP088911. Epub 2021 Jan 7.
What is the central question of this study? Is mesenchymal stem cell-conditioned medium capable of improving the pathological alterations of ovalbumin-induced asthma in mice? What is the main finding and its importance? Our study indicated that human amniotic membrane mesenchymal stem cell-conditioned medium is capable of modulating inflammation, fibrosis, oxidative stress and the pathological consequences of ovalbumin-induced allergic asthma in mice.
Paracrine factors secreted by mesenchymal stem cells (MSCs) have immunomodulatory, anti-inflammatory and antifibrotic properties, and the conditioned medium (CM) of these cells might have functional capabilities. We examined the effects of human amniotic membrane MSC-CM (hAM-MSC-CM) on ovalbumin (OVA)-induced asthma. Forty male Balb/c mice were randomly divided into the following four groups: control; OVA (sensitized and challenged with OVA); OVA+CM (sensitized and challenged with OVA and treated with hAM-MSC-CM); and OVA+Placebo (sensitized and challenged with OVA and treated with placebo). Forty-eight hours after the last challenge, serum and bronchoalveolar lavage fluid samples were collected and used for evaluation of inflammatory factors and cells, respectively. Lung tissue sections were stained with Haematoxylin and Eosin or Masson's Trichrome to evaluate pathological changes, and oxidative stress was assessed in fresh lung tissues. Treatment with hAM-MSC-CM significantly hindered histopathological changes and fibrosis and reduced the total cell count and the percentage of eosinophils and neutrophils in bronchoalveolar lavage fluid. Furthermore, it reduced serum levels of immunoglobulin E, interleukin-4, transforming growth factor-β and lung malondialdehyde. It also increased serum levels of interferon-γ and interleukin-10, in addition to the enzymatic activity of glutathione peroxidase, catalase and superoxide dismutase in lung tissue in comparison to the OVA and OVA+Placebo groups. This study showed that administration of hAM-MSC-CM can improve pathological conditions, such as inflammation, fibrosis and oxidative stress, in OVA-induced allergic asthma.
本研究的核心问题是什么?间充质干细胞条件培养基能否改善卵清蛋白诱导的哮喘小鼠的病理改变?主要发现及其重要性是什么?我们的研究表明,人羊膜间充质干细胞条件培养基能够调节炎症、纤维化、氧化应激和卵清蛋白诱导的过敏性哮喘的病理后果。
间充质干细胞(MSCs)分泌的旁分泌因子具有免疫调节、抗炎和抗纤维化特性,这些细胞的条件培养基(CM)可能具有功能能力。我们研究了人羊膜间充质干细胞 CM(hAM-MSC-CM)对卵清蛋白(OVA)诱导的哮喘的影响。40 只雄性 Balb/c 小鼠被随机分为以下四组:对照组;OVA(用 OVA 致敏和激发);OVA+CM(用 OVA 致敏和激发并用 hAM-MSC-CM 处理);OVA+安慰剂(用 OVA 致敏和激发并用安慰剂处理)。末次激发后 48 小时,收集血清和支气管肺泡灌洗液样本,分别用于评估炎症因子和细胞。用苏木精和伊红或 Masson 三色染色法对肺组织切片进行染色,以评估病理变化,并评估新鲜肺组织中的氧化应激。用 hAM-MSC-CM 处理可显著抑制组织病理学变化和纤维化,并减少支气管肺泡灌洗液中的总细胞计数和嗜酸性粒细胞和中性粒细胞的百分比。此外,与 OVA 和 OVA+安慰剂组相比,它还降低了血清免疫球蛋白 E、白细胞介素-4、转化生长因子-β和肺组织丙二醛水平。它还增加了血清干扰素-γ和白细胞介素-10水平,以及肺组织中谷胱甘肽过氧化物酶、过氧化氢酶和超氧化物歧化酶的酶活性。本研究表明,给予 hAM-MSC-CM 可改善 OVA 诱导的过敏性哮喘中的炎症、纤维化和氧化应激等病理状况。