EPR oxygen mapping (EPROM) of engineered cartilage grown in a hollow-fiber bioreactor

被引:21
作者
Ellis, SJ
Velayutham, M
Velan, SS
Petersen, EF
Zweier, JL
Kuppusamy, P
Spencer, RGS
机构
[1] NIA, Nucl Magnet Resonance Unit, NIH, Gerontol Res Ctr, Baltimore, MD 21224 USA
[2] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Div Cardiol,EPR Ctr, Baltimore, MD 21205 USA
关键词
EPR; cartilage; chondrocytes; oximetry; oxygen mapping;
D O I
10.1002/mrm.1262
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 [临床医学]; 100207 [影像医学与核医学]; 1009 [特种医学];
摘要
A novel electron paramagnetic resonance (EPR)-based oxygen mapping procedure (EPROM) is applied to cartilage grown in a single-, hollow-fiber bioreactor (HFBR) system. Chondrocytes harvested from the sterna of 17-day-old chick embryos were inoculated into an HFBR and produced hyaline cartilage over a period of 4 weeks. Tissue oxygen maps were generated according to the EPROM technique (Velan et al., Magn Reson Med 2000;43:804-809) by making use of the line-broadening effects of oxygen on the signal generated from nitroxide spin probes. In addition, the effect on oxygen consumption of the addition of cyanide to the tissue was investigated. Cyanide is a potent inhibitor of oxidative phosphorylation, and accordingly, given the constant provision of oxygen to the tissue, it would be expected to increase oxygen levels within the HFBR. The EPROM measurements showed a significant increase in oxygen concentration In the cartilage after the addition of cyanide. In contrast to other methods for studying oxygen in cartilage, EPROM can provide direct, noninvasive visualization of local concentrations in three dimensions. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:819 / 826
页数:8
相关论文
共 53 条
[1]
Oxygen and lactate concentrations measured in vivo in the intervertebral discs of patients with scoliosis and back pain [J].
Bartels, EM ;
Fairbank, JCT ;
Winlove, CP ;
Urban, JPG .
SPINE, 1998, 23 (01) :1-7
[2]
Bartsch P, 1966, Z Med Labortech, V7, P342
[3]
BATES EJ, 1984, BIOCHEM INT, V8, P629
[4]
DEDIFFERENTIATED CHONDROCYTES REEXPRESS THE DIFFERENTIATED COLLAGEN PHENOTYPE WHEN CULTURED IN AGAROSE GELS [J].
BENYA, PD ;
SHAFFER, JD .
CELL, 1982, 30 (01) :215-224
[5]
Eaton GR., 1991, EPR imaging and in vivo EPR
[6]
EXPRESSION OF MESSENGER-RNAS FOR COLLAGENS AND OTHER MATRIX COMPONENTS IN DEDIFFERENTIATING AND REDIFFERENTIATING HUMAN CHONDROCYTES IN CULTURE [J].
ELIMA, K ;
VUORIO, E .
FEBS LETTERS, 1989, 258 (02) :195-198
[7]
EMEL'YANOV N A, 1971, Ukrayins'kyi Biokhimichnyi Zhurnal, V43, P390
[8]
Sensitivity of chondrocytes of growing cartilage to reactive oxygen species [J].
Fragonas, E ;
Pollesello, P ;
Mlinarik, V ;
Toffanin, R ;
Grando, C ;
Godeas, C ;
Vittur, F .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1998, 1425 (01) :103-111
[9]
OXYGEN RADICALS, INFLAMMATION, AND ARTHRITIS - PATHOPHYSIOLOGICAL CONSIDERATIONS AND IMPLICATIONS FOR TREATMENT [J].
GREENWALD, RA .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 1991, 20 (04) :219-240
[10]
IMAGING RADIO-FREQUENCY ELECTRON-SPIN-RESONANCE SPECTROMETER WITH HIGH-RESOLUTION AND SENSITIVITY FOR INVIVO MEASUREMENTS [J].
HALPERN, HJ ;
SPENCER, DP ;
VANPOLEN, J ;
BOWMAN, MK ;
NELSON, AC ;
DOWEY, EM ;
TEICHER, BA .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1989, 60 (06) :1040-1050