Biomaterial implants mediate autologous stem cell recruitment in mice

被引:44
作者
Nair, A. [1 ,2 ]
Shen, J. [1 ,2 ]
Lotfi, P. [1 ,2 ]
Ko, C. -Y. [1 ,2 ]
Zhang, C. C. [3 ,4 ]
Tang, L. [1 ,2 ]
机构
[1] Univ Texas Arlington, Dept Bioengn, Arlington, TX 76019 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Bioengn, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Dev Biol, Dallas, TX 75390 USA
关键词
Autologous stem cells; Hematopoietic stem cells; Mesenchymal stem cells; Foreign body response; Flow cytometry; HEMATOPOIETIC PROGENITOR CELLS; STEM/PROGENITOR CELLS; INTERNATIONAL-SOCIETY; STROMAL CELLS; DIFFERENTIATION; THERAPY; REGENERATION; MOBILIZATION; HOST; MONOCYTES/MACROPHAGES;
D O I
10.1016/j.actbio.2011.06.050
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Autologous stem cells, recognized as the best cells for stem cell therapy, are associated with difficult extraction procedures which often lead to more traumas for the patients and time-consuming laboratory work, which delays their subsequent application. To combat such challenges, it was recently uncovered that, shortly after biomaterial implantation, following the recruitment of inflammatory cells, substantial numbers of mesenchymal stem cells (MSC) and hematopoietic stem cells (HSC) were recruited to the implantation sites. These multipotent MSC could be differentiated into various lineages in vitro. Inflammatory signals may be responsible for the gathering of stem cells, since there is a good relationship between biomaterial-mediated inflammatory responses and stem cell accumulation in vivo. In addition, the treatment with the anti-inflammatory drug dexamethasone substantially reduced the recruitment of both MSC and HSC. The results from this work support that such strategies could be further developed towards localized recruitment and differentiation of progenitor cells. This may permit the future development of autologous stem cell therapies without the need for tedious cell isolation, culture and transplantation. (C) 2011 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3887 / 3895
页数:9
相关论文
共 77 条
[1]
Abramoff M.D., 2004, Biophotonics International, V11, P36
[2]
Pathological axes of wound repair: Gastrulation revisited [J].
Aller, Maria-Angeles ;
Arias, Jose-Ignacio ;
Arias, Jaime .
THEORETICAL BIOLOGY AND MEDICAL MODELLING, 2010, 7
[3]
Induced pluripotent stem cells: current progress and potential for regenerative medicine [J].
Amabile, Giovanni ;
Meissner, Alexander .
TRENDS IN MOLECULAR MEDICINE, 2009, 15 (02) :59-68
[4]
Nonhematopoietic/endothelial SSEA-1+ cells define the most primitive progenitors in the adult murine bone marrow mesenchymal compartment [J].
Anjos-Afonso, Fernando ;
Bonnet, Dominique .
BLOOD, 2007, 109 (03) :1298-1306
[5]
Aging of mesenchymal stem cell in vitro [J].
Bonab, MM ;
Alimoghaddam, K ;
Talebian, F ;
Ghaffari, SH ;
Ghavamzadeh, A ;
Nikbin, B .
BMC CELL BIOLOGY, 2006, 7 (1)
[6]
Bone regeneration by implantation of purified, culture-expanded human mesenchymal stem cells [J].
Bruder, SP ;
Kurth, AA ;
Shea, M ;
Hayes, WC ;
Jaiswal, N ;
Kadiyala, S .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1998, 16 (02) :155-162
[7]
CIRCULATING FIBROCYTES DEFINE A NEW LEUKOCYTE SUBPOPULATION THAT MEDIATES TISSUE-REPAIR [J].
BUCALA, R ;
SPIEGEL, LA ;
CHESNEY, J ;
HOGAN, M ;
CERAMI, A .
MOLECULAR MEDICINE, 1994, 1 (01) :71-81
[8]
Bone marrow mesenchymal stem cells upregulate transient outward potassium currents in postnatal rat ventricular myocytes [J].
Cai Benzhi ;
Zhao Limei ;
Wang Ning ;
Liu Jiaqi ;
Zhu Songling ;
Meng Fanyu ;
Zhou Hongyu ;
Lu Yanjie ;
Ai Jing ;
Yang Baofeng .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2009, 47 (01) :41-48
[9]
Concise review: Mesenchymal stem cells: Their phenotype, differentiation capacity, immunological features, and potential for homing [J].
Chamberlain, Giselle ;
Fox, James ;
Ashton, Brian ;
Middleton, Jim .
STEM CELLS, 2007, 25 (11) :2739-2749
[10]
Effects of anti-inflammatory drugs on proliferation, cytotoxicity and osteogenesis in bone marrow mesenchymal stem cells [J].
Chang, Je-Ken ;
Li, Ching-Ju ;
Wu, Shun-Cheng ;
Yeh, Ching-Hua ;
Chen, Chung-Hwan ;
Fu, Yin-Chih ;
Wang, Gwo-Jaw ;
Ho, Mei-Ling .
BIOCHEMICAL PHARMACOLOGY, 2007, 74 (09) :1371-1382