The recruitment of primitive Lin- Sea-1+, CD34+, c-kit+ and CD271+ cells during the early intraperitoneal foreign body reaction

被引:19
作者
Vranken, Ilse [1 ]
De Visscher, Geofrey [1 ]
Lebacq, An [1 ]
Verbeken, Erik [2 ]
Flameng, Willem [1 ]
机构
[1] Katholieke Univ Leuven, Dept Cardiovasc Dis, Lab Expt Cardiac Surg, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Div Med Diagnost Sci, Dept Morphol & Mol Pathol, B-3000 Louvain, Belgium
关键词
foreign body response; inflammation; cell adhesion; primitive cell;
D O I
10.1016/j.biomaterials.2007.10.041
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Implanted materials, such as medical devices, provoke the body to initiate an inflammatory reaction, known as the foreign body reaction (FBR), which causes Several complications for example in hip prostheses, silicone implants, peritoneal dialysis catheters and left ventricular assist devices. FBR is initiated by macrophage adherence and results in granulation tissue formation. The early immunobiology and development of this tissue is not completely understood, but there are indications from related myofibroblast-forming diseases such as vascular repair and fibrosis that primitive stem cells also play a role in the formation of FBR-tissue. To investigate this, acellular photo-oxidized bovine pericardium patches were implanted intraperitoneally in rats and retrieved at time-points ranging from 6 h to 7 days. A significant fraction of Sca-1(+) (6 h-2 days), c-kit(+), CD34(+) and CD271(+) (2-3 days) stem/progenitor cells were detected. Colony-forming and differentiation capacity of the primitive stem cells into adipo-, osteo-, and myofibroblasts were shown. The presence of these primitive cells and their myofibroblastic differentiation potential were also confirmed at RNA level. The identification of specific primitive cells during FBR may have important implications for the inflammatory responses to inert materials and their use in tissue prostheses. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:797 / 808
页数:12
相关论文
共 48 条
[31]   CATHETER COMPLICATIONS ASSOCIATED WITH IMPLANTABLE SYSTEMS FOR PERITONEAL INSULIN DELIVERY - AN ANALYSIS OF FREQUENCY, PREDISPOSING FACTORS, AND OBSTRUCTING MATERIALS [J].
RENARD, E ;
BALDET, P ;
PICOT, MC ;
JACQUESAPOSTOL, D ;
LAUTON, D ;
COSTALAT, G ;
BRINGER, J ;
JAFFIOL, C .
DIABETES CARE, 1995, 18 (03) :300-306
[32]  
Rhodes NP, 1997, J BIOMED MATER RES, V37, P481, DOI 10.1002/(SICI)1097-4636(19971215)37:4<481::AID-JBM6>3.0.CO
[33]  
2-H
[34]   Primary murine MSC show highly efficient homing to the bone marrow but lose homing ability following culture [J].
Rombouts, WJC ;
Ploemacher, RE .
LEUKEMIA, 2003, 17 (01) :160-170
[35]   Inflammatory reaction dependence on implant localization in rat soft tissue models [J].
Rosengren, A ;
Danielsen, N ;
Bjursten, LM .
BIOMATERIALS, 1997, 18 (14) :979-987
[36]   The human hematopoietic stem cell compartment is heterogeneous for CXCR4 expression [J].
Rosu-Myles, M ;
Gallacher, L ;
Murdoch, B ;
Hess, DA ;
Keeney, M ;
Kelvin, D ;
Dale, L ;
Ferguson, SSG ;
Wu, DM ;
Fellows, F ;
Bhatia, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14626-14631
[37]   Circulating vascular progenitor cells contribute to vascular repair, remodeling, and lesion formation [J].
Sata, M .
TRENDS IN CARDIOVASCULAR MEDICINE, 2003, 13 (06) :249-253
[38]   Crucial role of stromal cell-derived factor-1α in neointima formation after vascular injury in apolipoprotein E-deficient mice [J].
Schober, A ;
Knarren, S ;
Lietz, M ;
Lin, EA ;
Weber, C .
CIRCULATION, 2003, 108 (20) :2491-2497
[39]   The myofibroblast -: A quarter century after its discovery [J].
Schürch, W ;
Seemayer, TA ;
Gabbiani, G .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (02) :141-147
[40]  
SPANGRUDE GJ, 1991, BLOOD, V78, P1395