Efficient and stable retroviral transfection of ovine endothelial cells with green fluorescent protein for cardiovascular tissue engineering

被引:9
作者
Afting, M
Stock, UA
Nasseri, B
Pomerantseva, I
Seed, B
Vacanti, JP
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Surg,Lab Tissue Engn & Organ Fabricat, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Mol Biol, Boston, MA 02114 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Integrat Med & Innovat Technol, Boston, MA 02114 USA
来源
TISSUE ENGINEERING | 2003年 / 9卷 / 01期
关键词
D O I
10.1089/107632703762687618
中图分类号
Q813 [细胞工程];
学科分类号
摘要
To determine whether cellular components of tissue-engineered cardiovascular structures are derived from cells harvested and seeded onto an acellular scaffold, or from cells originating from surrounding tissue (e.g., proximal and distal anastomosis), cellular retroviral transfection with green fluorescent protein (GFP) was used. Ovine endothelial cells (ECs) were transfected with a Moloney murine leukemia virus (Mo-MuLV)-based retroviral vector expressing GFP. Transfection was evaluated by fluorescence microscopy and fluorescence-activated cell sorting. The rate of transfection of the primary cells was 33.4% for ECs, 48 hours after transfection. Stable transfection could be observed for at least 25 subsequent passages. Retroviral transfection with GFP enables stable and reliable long-term labeling of ovine ECs. This approach might offer an attractive pathway to study tissue development, with emphasis on distinguishing between cellular components initially seeded onto a construct and those occurring as a result of cell ingrowth from surrounding tissue.
引用
收藏
页码:137 / 141
页数:5
相关论文
共 15 条
[1]   Optimizing fluorescent labeling of endothelial cells for tracking during long-term studies of autologous transplantation [J].
Fox, D ;
Kouris, GJ ;
Blumofe, KA ;
Heilizer, TJ ;
Husak, V ;
Greisler, HP .
JOURNAL OF SURGICAL RESEARCH, 1999, 86 (01) :9-16
[2]   FLUORESCENT CARBOCYANINE DYES ALLOW LIVING NEURONS OF IDENTIFIED ORIGIN TO BE STUDIED IN LONG-TERM CULTURES [J].
HONIG, MG ;
HUME, RI .
JOURNAL OF CELL BIOLOGY, 1986, 103 (01) :171-187
[3]   Neural toxicity of retroviruses [J].
Hurley, MJ ;
Bradford, HF ;
OHare, K ;
Stern, GM ;
Uchida, K .
NEUROSCIENCE LETTERS, 1996, 220 (01) :66-68
[4]   Rapid retroviral infection of human haemopoietic cells of different lineages:: efficient transfer in fresh T cells [J].
Introna, M ;
Barbui, AM ;
Golay, J ;
Bambacioni, F ;
Schirò, R ;
Bernasconi, S ;
Breviario, F ;
Erba, E ;
Borleri, G ;
Barbui, T ;
Biondi, A ;
Rambaldi, A .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (02) :449-461
[5]   CULTURE OF HUMAN ENDOTHELIAL CELLS DERIVED FROM UMBILICAL VEINS - IDENTIFICATION BY MORPHOLOGIC AND IMMUNOLOGICAL CRITERIA [J].
JAFFE, EA ;
NACHMAN, RL ;
BECKER, CG ;
MINICK, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1973, 52 (11) :2745-2756
[6]  
KINGSTON RE, 1998, CURRENT PROTOCOLS MO
[7]   TISSUE ENGINEERING [J].
LANGER, R ;
VACANTI, JP .
SCIENCE, 1993, 260 (5110) :920-926
[8]   Evidence for circulating bone marrow-derived endothelial cells [J].
Shi, Q ;
Rafii, S ;
Wu, MHD ;
Wijelath, ES ;
Yu, C ;
Ishida, A ;
Fujita, Y ;
Kothari, S ;
Mohle, R ;
Sauvage, LR ;
Moore, MAS ;
Storb, RF ;
Hammond, WP .
BLOOD, 1998, 92 (02) :362-367
[9]   Transplantation of a tissue-engineered pulmonary artery. [J].
Shin'oka, T ;
Imai, Y ;
Ikada, Y .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (07) :532-533
[10]   Creation of viable pulmonary artery autografts through tissue engineering [J].
Shinoka, T ;
Shum-Tim, D ;
Ma, PX ;
Tanel, RE ;
Isogai, N ;
Langer, R ;
Vacanti, JP ;
Mayer, JE .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1998, 115 (03) :536-545