Spleen lymphocyte kinetics in mice under normal and inflammatory conditions:: An application of the transgenic mouse expressing β-galactosidase (ROSA 26)

被引:3
作者
Hosoya, K
Takashima, H
Matsuda, K
Terasaki, T [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Dept Mol Biopharm & Genet, Sendai, Miyagi 980, Japan
[2] Tohoku Univ, New Ind Creat Hatchery, Aoba Ku, Sendai, Miyagi 9808578, Japan
[3] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Toyama 9300194, Japan
关键词
cell kinetic; cell delivery; ROSA; 26; mouse; beta-galactosidase;
D O I
10.1248/bpb.25.1378
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to develop a method for the measurement of the cell kinetics of spleen lymphocytes using the ROSA 26 transgenic mouse ubiquitously expressing beta-galactosidase (beta-gal). Spleen lymphocytes were isolated from ROSA 26 mice and intravenously inoculated into C57BL/6 mice under normal conditions and inflammatory conditions following lipopolysaccharide (LPS) treatment. Spleen lymphocyte accumulation in tissues was determined as a measurement of beta-gal activity. Spleen lymphocytes isolated from ROSA 26 mice have beta-gal activities of 1.45 x 10(-4) pg per cell. A good correlation between beta-gal activities and cell numbers was obtained (r(2) = 0.999) over the range 1 x 10(3) to 1 x 10(7) cells, corresponding to 70 fg to 350 pg beta-gal activity. Spleen lymphocytes (4 x 10(7) cells) were intravenously inoculated into normal mice and subsequently each tissue was isolated and the corresponding beta-gal activity measured. Spleen lymphocyte accumulation was relatively high in the spleen and lymph nodes. The accumulated spleen lymphocyte cell number was 1.39 x 10(7) cells/g spleen and 5.45 x 10(7) cells/g lymph node 1 h and 6 h after inoculation, respectively, and this remained constant up to 24 h. In the lung, lymphocyte accumulation was 3.98 x 10(7) cells/g tissue 10 min after inoculation then gradually fell to 7.09 x 10(5) cells/g tissue after 24 h. In addition, the femoral muscle following intramuscular injection of LPS showed a high accumulation of spleen lymphocytes, whereas the untreated and contralateral femoral muscle had the same level as the background. In conclusion, spleen lymphocytes isolated from ROSA 26 mice can be used to measure beta-gal activity and the sensitivity is relatively high over the 70 fg to 350 pg range. This suggests that cells isolated from the ROSA 26 mouse can be applied to the study of cell kinetics.
引用
收藏
页码:1378 / 1380
页数:3
相关论文
共 14 条
[1]   1,2-DIOXETANES - NOVEL CHEMI-LUMINESCENT ENZYME SUBSTRATES - APPLICATIONS TO IMMUNOASSAYS [J].
BRONSTEIN, I ;
EDWARDS, B ;
VOYTA, JC .
JOURNAL OF BIOLUMINESCENCE AND CHEMILUMINESCENCE, 1989, 4 (01) :99-111
[2]   A role for lymphocytes and cytokines on the eosinophil migration induced by LPS [J].
Castro-Faria-Neto, HC ;
Penido, CM ;
Larangeira, AP ;
Silva, AR ;
Bozza, PT .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1997, 92 :197-200
[3]   DETERMINATION OF THE ORIGIN AND NATURE OF BRAIN MACROPHAGES AND MICROGLIAL CELLS IN MOUSE CENTRAL-NERVOUS-SYSTEM, USING NONRADIOACTIVE INSITU HYBRIDIZATION AND IMMUNOPEROXIDASE TECHNIQUES [J].
DEGROOT, CJA ;
HUPPES, W ;
SMINIA, T ;
KRAAL, G ;
DIJKSTRA, CD .
GLIA, 1992, 6 (04) :301-309
[4]   PROMOTER TRAPS IN EMBRYONIC STEM-CELLS - A GENETIC SCREEN TO IDENTIFY AND MUTATE DEVELOPMENTAL GENES IN MICE [J].
FRIEDRICH, G ;
SORIANO, P .
GENES & DEVELOPMENT, 1991, 5 (09) :1513-1523
[5]   A CHEMILUMINESCENT ASSAY FOR QUANTITATION OF BETA-GALACTOSIDASE IN THE FEMTOGRAM RANGE - APPLICATION TO QUANTITATION OF BETA-GALACTOSIDASE IN IACZ-TRANSFECTED CELLS [J].
JAIN, VK ;
MAGRATH, IT .
ANALYTICAL BIOCHEMISTRY, 1991, 199 (01) :119-124
[6]   Kinetics of central nervous system microglial and macrophage engraftment: Analysis using a transgenic bone marrow transplantation model [J].
Kennedy, DW ;
Abkowitz, JL .
BLOOD, 1997, 90 (03) :986-993
[7]   Ubiquitous expression of marker transgenes in mice and rats [J].
Kisseberth, WC ;
Brettingen, NT ;
Lohse, JK ;
Sandgren, EP .
DEVELOPMENTAL BIOLOGY, 1999, 214 (01) :128-138
[8]  
KRALL WJ, 1994, BLOOD, V83, P2737
[9]  
MATHEW LT, 1987, NUCL MED BIOL, V14, P51
[10]   STUDIES OF H-2KB MUTANT MICE .2. DEFINITION OF NEW H-2 SPECIFICITIES (H-2,68,69,71,72) USING THE H-2KB MUTANT, B6.C-H-2BM10 [J].
MORGAN, GM ;
MCKENZIE, IFC ;
MELVOLD, RW .
IMMUNOGENETICS, 1980, 11 (01) :43-53