4.2 Article

The Therapeutic Effect of ICAM 1 Overexpressing Mesenchymal Stem Cells on Acute Graft-Versus-Host Disease

期刊

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 46, 期 6, 页码 2624-2635

出版社

KARGER
DOI: 10.1159/000489689

关键词

Mesenchymal stem cells; Intercellular adhesion molecule-1; Graft-versus-host disease; Bone marrow transplantation; Murine GVHD model

资金

  1. National Key and Development Program of China [2016YFC1000305]
  2. Origin cell Technology Group grant

向作者/读者索取更多资源

Background/Aims: Mesenchymal stem cells (MSCs) do not readily migrate to appropriate sites, and this creates a major obstacle for their use in the treatment of graft-versus-host disease (GVHD). Intercellular adhesion molecule-1 (ICAM-1) can guide the homing of various immune cells to the proper anatomical location within secondary lymphoid organs (SLOs), which are the major niches for generating immune responses or tolerance. MSCs rarely migrate to SLOs after intravenous infusion, and are constitutively low expression of ICAM-1. So in our previous work, ICAM-1 was engineered into a murine MSC line C3H10T1/2 by retrovirus transfection system (ICAM-1MSCs). Here, we hypothesized that ICAM-1(high)MSCs may significantly improve their immunomodulatory effect. Methods: We used different co-culture methods combined with real-time PCR and flow cytometry to evaluate ICAM-1(high)MSCs immunomodulatory effect on dendritic cells (DCs) and T cells in vitro and in vivo, MSCs were labeled with carboxyfluorescein diacetate succinimidylester (CFSE) to detect its distribution in mouse model. Results: Our in vitro analyses revealed ICAM-1 MSCs could suppress DCs maturation according to co-culture methods and suppress the T cell immune response according to the mixed lymphocyte response (MLR) and lymphoblast transformation test (LTT) tests. We found that infusion of ICAM-1h'ghMSCs potently prolonged the survival of GVHD mouse model. The infused ICAM 1h'oMSCs migrate to SLOs in vivo, and suppressed DCs maturation, suppressed CD4+ T cell differentiation to Thl cells, and increased the ratios of Treg cells. Conclusions: Taken together, these data demonstrate that ICAM-lhqhMSCs had an enhanced immunosuppressive effect on DCs and T cells, which may help explain the protective effect in a GVHD model. This exciting therapeutic strategy may improve the clinical efficacy of MSC-based therapy for GVHD. (C) 2018 The Author(s) Published by S Karger AG, Basel.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Biochemistry & Molecular Biology

Drosophila p24 and Sec22 regulate Wingless trafficking in the early secretory pathway

Xue Li, Yihui Wu, Chenghao Shen, Tatyana Y. Belenkaya, Lorraine Ray, Xinhua Lin

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2015)

Article Cell Biology

The Drosophila tankyrase regulates Wg signaling depending on the concentration of Daxin

Ying Feng, Xue Li, Lorraine Ray, Haiyun Song, Jia Qu, Shuyong Lin, Xinhua Lin

CELLULAR SIGNALLING (2014)

Article Cell Biology

Effects of Early MSC Intervention on Preventing the Streptozotocin-Induced T1DM Progression in Mice

Lanlan Zha, Xue Li, Xiangyu Meng, Yuanlin Liu, Weijiang Liu, Yang Wang, Yue Fan, Bin Zhou, Pei Li, Rongxiu Zheng, Yi Zhang

OXIDATIVE MEDICINE AND CELLULAR LONGEVITY (2020)

Article Cell Biology

Wip1 regulates the immunomodulatory effects of murine mesenchymal stem cells in type 1 diabetes mellitus via targeting IFN-α/BST2

Na Zhou, Weijiang Liu, Wei Zhang, Yuanlin Liu, Xue Li, Yang Wang, Rongxiu Zheng, Yi Zhang

Summary: This study reveals the crucial role of Wip1 in modulating the immunosuppressive capacities of MSCs in T1DM mice, showing that Wip1(-/-)MSCs have weaker therapeutic effects and immunosuppressive capabilities. The findings suggest that Wip1 is essential for regulating the immunomodulation properties of MSCs in T1DM treatment.

CELL DEATH DISCOVERY (2021)

暂无数据