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Immunobiology of mesenchymal stem cells.

作者信息

Ma S, Xie N, Li W, Yuan B, Shi Y, Wang Y

机构信息

Key Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences of Chinese Academy of Sciences/Shanghai Jiao Tong University School of Medicine, 225 South Chongqing Road, Shanghai 200025, China.

National Institutes for Food and Drug Control, No. 2 Tiantan Xili, Beijing 100050, China.

出版信息

Cell Death Differ. 2014 Feb;21(2):216-25. doi: 10.1038/cdd.2013.158. Epub 2013 Nov 1.


DOI:10.1038/cdd.2013.158
PMID:24185619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3890955/
Abstract

Mesenchymal stem cells (MSCs) can be isolated from almost all tissues and effectively expanded in vitro. Although their true in situ properties and biological functions remain to be elucidated, these in vitro expanded cells have been shown to possess potential to differentiate into specific cell lineages. It is speculated that MSCs in situ have important roles in tissue cellular homeostasis by replacing dead or dysfunctional cells. Recent studies have demonstrated that in vitro expanded MSCs of various origins have great capacity to modulate immune responses and change the progression of different inflammatory diseases. As tissue injuries are often accompanied by inflammation, inflammatory factors may provide cues to mobilize MSCs to tissue sites with damage. Before carrying out tissue repair functions, MSCs first prepare the microenvironment by modulating inflammatory processes and releasing various growth factors in response to the inflammation status. In this review, we focus on the crosstalk between MSCs and immune responses and their potential clinical applications, especially in inflammatory diseases.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/99d2f08960a0/cdd2013158f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/1b6bf2936d3f/cdd2013158f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/f4e544e983b6/cdd2013158f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/cae955b6af91/cdd2013158f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/99d2f08960a0/cdd2013158f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/1b6bf2936d3f/cdd2013158f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/f4e544e983b6/cdd2013158f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/cae955b6af91/cdd2013158f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/3890955/99d2f08960a0/cdd2013158f4.jpg

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Immunobiology of mesenchymal stem cells.

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[5]
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[6]
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[7]
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[10]
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本文引用的文献

[1]
Inflammatory pre-conditioning of mesenchymal multipotent stromal cells improves their immunomodulatory potency in acute pyelonephritis in rats.

Cytotherapy. 2013-4-2

[2]
Human mesenchymal stem cells increases expression of α-tubulin and angiopoietin 1 and 2 in focal cerebral ischemia and reperfusion.

Curr Neurovasc Res. 2013-5

[3]
Adoptive transfer of human gingiva-derived mesenchymal stem cells ameliorates collagen-induced arthritis via suppression of Th1 and Th17 cells and enhancement of regulatory T cell differentiation.

Arthritis Rheum. 2013-5

[4]
Different roles of PD-L1 and FasL in immunomodulation mediated by human placenta-derived mesenchymal stem cells.

Hum Immunol. 2012-12-20

[5]
Impaired therapeutic capacity of autologous stem cells in a model of type 2 diabetes.

Stem Cells Transl Med. 2012-1-26

[6]
Models of hemorrhagic shock: differences in the physiological and inflammatory response.

Cytokine. 2012-11-22

[7]
CCR2-dependent recruitment of macrophages by tumor-educated mesenchymal stromal cells promotes tumor development and is mimicked by TNFα.

Cell Stem Cell. 2012-11-15

[8]
Hypoxia-induced secretion of TGF-β1 in mesenchymal stem cell promotes breast cancer cell progression.

Cell Transplant. 2012-10-12

[9]
Mesenchymal stem cells repress Th17 molecular program through the PD-1 pathway.

PLoS One. 2012-9-17

[10]
Intravenous mesenchymal stem cells prevented rejection of allogeneic corneal transplants by aborting the early inflammatory response.

Mol Ther. 2012-8-28

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