Surgically relevant aspects of stem cell paracrine effects

被引:68
作者
Crisostomo, Paul R. [1 ]
Markel, Troy A. [1 ]
Wang, Yue [1 ]
Meldrum, Daniel R. [1 ,2 ,3 ]
机构
[1] Indiana Univ, Sch Med, Dept Surg, Indianapolis, IN 46204 USA
[2] Indiana Univ, Sch Med, Dept Physiol, Indianapolis, IN 46204 USA
[3] Indiana Univ, Sch Med, Ctr Immunol, Indianapolis, IN 46204 USA
关键词
D O I
10.1016/j.surg.2007.10.015
中图分类号
R61 [外科手术学];
学科分类号
摘要
STEM CELLs are undifferentiated, self-renewing, and multipotent (able to differentiate into multiple cell types). Unlike traditional treatment modalities, these unique characteristics may enable stem cells to undo irreversible cellular damage and rebuild injured or diseased tissue. Recent evidence suggests that stem cells may influence positively the recovery from injury via paracrine factors that promote tissue repair. Insights into paracrine mechanisms of stem cells may help the surgeon scientist devise more effective therapies and earlier widespread application. This review 1) unravels the pathways for stem cell-mediated paracrine protection; 2) highlights the growth factors and cytokines expressed; and 3) explores the potential of using stem cells clinically.
引用
收藏
页码:577 / 581
页数:5
相关论文
共 9 条
[1]   Gender differences in injury induced mesenchymal stem cell apoptosis and VEGF, TNF, IL-6 expression: Role of the 55 kDa TNF receptor (TNFR1) [J].
Crisostomo, Paul R. ;
Wang, Meijing ;
Herring, Christine M. ;
Markel, Troy A. ;
Meldrum, Kirstan K. ;
Lillemoe, Keith D. ;
Meldrum, Daniel R. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2007, 42 (01) :142-149
[2]  
CRISOSTOMO PR, IN PRESS SURGERY
[3]   Supportive interaction between cell survival signaling and angiocompetent factors enhances donor cell survival and promotes angiomyogenesis for cardiac repair [J].
Jiang, Shujia ;
Haider, Husnain Kh. ;
Idris, Niagara M. ;
Salim, Asmat ;
Ashraf, Muhammad .
CIRCULATION RESEARCH, 2006, 99 (07) :776-784
[4]  
MARKEL TA, IN PRESS AM J PHYSL
[5]   Haematopoietic stem cells do not transdifferentiate into cardiac myocytes in myocardial infarcts [J].
Murry, CE ;
Soonpaa, MH ;
Reinecke, H ;
Nakajima, H ;
Nakajima, HO ;
Rubart, M ;
Pasumarthi, KBS ;
Virag, JI ;
Bartelmez, SH ;
Poppa, V ;
Bradford, G ;
Dowell, JD ;
Williams, DA ;
Field, LJ .
NATURE, 2004, 428 (6983) :664-668
[6]   Bone marrow stem cells prevent left ventricular remodeling of ischemic heart through paracrine signaling [J].
Uemura, Ryota ;
Xu, Meifeng ;
Ahmad, Nauman ;
Ashraf, Muhammad .
CIRCULATION RESEARCH, 2006, 98 (11) :1414-1421
[7]   Signaling factors in stem cell-mediated repair of infarcted myocardium [J].
Vandervelde, S ;
van Luyn, MJA ;
Tio, RA ;
Harmsen, MC .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2005, 39 (02) :363-376
[8]   Human progenitor cells from bone marrow or adipose tissue produce VEGF, HGF, and IGF-I in response to TNF by a p38 MAPK-dependent mechanism [J].
Wang, Meijing ;
Crisostomo, Paul R. ;
Herring, Christine ;
Meldrum, Kirstan K. ;
Meldrum, Daniel R. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2006, 291 (04) :R880-R884
[9]   Pretreatment with adult progenitor cells improves recovery and decreases native myocardial proinflammatory signaling after ischemia [J].
Wang, MJ ;
Tsai, BM ;
Crisostomo, PR ;
Meldrum, DR .
SHOCK, 2006, 25 (05) :454-459