Concise Review: The Bystander Effect: Mesenchymal Stem Cell-Mediated Lung Repair

被引:56
作者
Savukinas, Ulrika Blank [1 ]
Enes, Sara Rolandsson [1 ]
Sjoland, Annika Andersson [1 ]
Westergren-Thorsson, Gunilla [1 ]
机构
[1] Lund Univ, Lung Biol Unit, Dept Expt Med Sci, Solvegatan 19,BMC C12, S-22184 Lund, Sweden
基金
英国医学研究理事会;
关键词
Mesenchymal stem cell; Lung; Regenerative medicine; Paracrine communication; Immunomodulation; Stem cell niche; ANGIOPOIETIN-1; GENE-THERAPY; STROMAL CELLS; BONE-MARROW; UMBILICAL-CORD; MITOCHONDRIAL DYSFUNCTION; EXTRACELLULAR VESICLES; MYOCARDIAL-INFARCTION; AIRWAY INFLAMMATION; MOUSE LUNG; ADULT LUNG;
D O I
10.1002/stem.2357
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Mesenchymal stem or stromal cells (MSCs), a heterogeneous subset of adult stem/progenitor cells, have surfaced as potential therapeutic units with significant clinical benefit for a wide spectrum of disease conditions, including those affecting the lung. Although MSCs carry both self-renewal and multilineage differentiation abilities, current dogma holds that MSCs mainly contribute to tissue regeneration and repair by modulating the host tissue via secreted cues. Thus, the therapeutic benefit of MSCs is thought to derive from so called bystander effects. The regenerative mechanisms employed by MSCs in the lung include modulation of the immune system as well as promotion of epithelial and endothelial repair. Apart from secreted factors, a number of recent findings suggest that MSCs engage in mitochondrial transfer and shedding of membrane vesicles as a means to enhance tissue repair following injury. Furthermore, it is becoming increasingly clear that MSCs are an integral component of epithelial lung stem cell niches. As such, MSCs play an important role in coupling information from the environment to stem and progenitor populations, such that homeostasis can be ensured even in the face of injury. It is the aim of this review to outline the major mechanisms by which MSCs contribute to lung regeneration, synthesizing recent preclinical findings with data from clinical trials and potential for future therapy.
引用
收藏
页码:1437 / 1444
页数:8
相关论文
共 97 条
[1]
Mitochondrial Dysfunction Increases Allergic Airway Inflammation [J].
Aguilera-Aguirre, Leopoldo ;
Bacsi, Attila ;
Saavedra-Molina, Alfredo ;
Kurosky, Alexander ;
Sur, Sanjiv ;
Boldogh, Istvan .
JOURNAL OF IMMUNOLOGY, 2009, 183 (08) :5379-5387
[2]
Miro1 regulates intercellular mitochondrial transport & enhances mesenchymal stem cell rescue efficacy [J].
Ahmad, Tanveer ;
Mukherjee, Shravani ;
Pattnaik, Bijay ;
Kumar, Manish ;
Singh, Suchita ;
Kumar, Manish ;
Rehman, Rakhshinda ;
Tiwari, Brijendra K. ;
Jha, Kumar A. ;
Barhanpurkar, Amruta P. ;
Wani, Mohan R. ;
Roy, Soumya S. ;
Mabalirajan, Ulaganathan ;
Ghosh, Balaram ;
Agrawal, Anurag .
EMBO JOURNAL, 2014, 33 (09) :994-1010
[3]
Mesenchymal stem cells promote alveolar epithelial cell wound repair in vitro through distinct migratory and paracrine mechanisms [J].
Akram, Khondoker M. ;
Samad, Sohel ;
Spiteri, Monica A. ;
Forsyth, Nicholas R. .
RESPIRATORY RESEARCH, 2013, 14
[4]
Contrasting Expression of Canonical Wnt Signaling Reporters TOPGAL, BATGAL and Axin2LacZ during Murine Lung Development and Repair [J].
Al Alam, Denise ;
Green, Melissa ;
Irani, Reza Tabatabai ;
Parsa, Sara ;
Danopoulos, Soula ;
Sala, Frederic G. ;
Branch, Jonathan ;
El Agha, Elie ;
Tiozzo, Caterina ;
Voswinckel, Robert ;
Jesudason, Edwin C. ;
Warburton, David ;
Bellusci, Saverio .
PLOS ONE, 2011, 6 (08)
[5]
Human mesenchymal stem cells alter antigen-presenting cell maturation and induce T-cell unresponsiveness [J].
Beyth, S ;
Borovsky, Z ;
Mevorach, D ;
Liebergall, M ;
Gazit, Z ;
Aslan, H ;
Galun, E ;
Rachmilewitz, J .
BLOOD, 2005, 105 (05) :2214-2219
[6]
Atmospheric Oxygen Inhibits Growth and Differentiation of Marrow-Derived Mouse Mesenchymal Stem Cells via a p53-Dependent Mechanism: Implications for Long-Term Culture Expansion [J].
Boregowda, Siddaraju V. ;
Krishnappa, Veena ;
Chambers, Jeremy W. ;
Lograsso, Philip V. ;
Lai, Wen-Tzu ;
Ortiz, Luis A. ;
Phinney, Donald G. .
STEM CELLS, 2012, 30 (05) :975-987
[7]
Association between mitochondrial dysfunction and severity and outcome of septic shock [J].
Brealey, D ;
Brand, M ;
Hargreaves, I ;
Heales, S ;
Land, J ;
Smolenski, R ;
Davies, NA ;
Cooper, CE ;
Singer, M .
LANCET, 2002, 360 (9328) :219-223
[8]
A phase 1b study of placenta-derived mesenchymal stromal cells in patients with idiopathic pulmonary fibrosis [J].
Chambers, Daniel C. ;
Enever, Debra ;
Ilic, Nina ;
Sparks, Lisa ;
Whitelaw, Kylie ;
Ayres, John ;
Yerkovich, Stephanie T. ;
Khalil, Dalia ;
Atkinson, Kerry M. ;
Hopkins, Peter M. A. .
RESPIROLOGY, 2014, 19 (07) :1013-1018
[9]
Mesenchymal Stem Cells for Bronchopulmonary Dysplasia: Phase 1 Dose-Escalation Clinical Trial [J].
Chang, Yun Sil ;
Ahn, So Yoon ;
Yoo, Hye Soo ;
Sung, Se In ;
Choi, Soo Jin ;
Oh, Won Il ;
Park, Won Soon .
JOURNAL OF PEDIATRICS, 2014, 164 (05) :966-+
[10]
Keratinocyte Growth Factor Gene Delivery via Mesenchymal Stem Cells Protects against Lipopolysaccharide-Induced Acute Lung Injury in Mice [J].
Chen, Jie ;
Li, Chunsun ;
Gao, Xiaofang ;
Li, Chonghui ;
Liang, Zhixin ;
Yu, Ling ;
Li, Yanqin ;
Xiao, Xiaoyi ;
Chen, Liangan .
PLOS ONE, 2013, 8 (12)