HIGH EXPRESSION OF HUMAN BETA-S-GLOBINS AND ALPHA-GLOBINS IN TRANSGENIC MICE - ERYTHROCYTE ABNORMALITIES, ORGAN DAMAGE, AND THE EFFECT OF HYPOXIA

被引:79
作者
FABRY, ME [1 ]
COSTANTINI, F [1 ]
PACHNIS, A [1 ]
SUZUKA, SM [1 ]
BANK, N [1 ]
AYNEDJIAN, HS [1 ]
FACTOR, SM [1 ]
NAGEL, RL [1 ]
机构
[1] COLUMBIA UNIV,DEPT GENET & DEV,NEW YORK,NY 10032
关键词
D O I
10.1073/pnas.89.24.12155
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A line of transgenic mice with two cointegrated transgenes, the human beta(S)- and alpha2-globin genes, linked to the beta-globin locus control region was produced and bred with mice carrying a deletion of the mouse beta(major)-globin gene. In transgenic mice homozygous for the beta(major) deletion (alpha(H)beta(S)[beta(MDD)]; where alpha(H) is human alpha-globin and MD is mouse deletion), 72.5 +/- 2.4% (mean +/- SD) of the beta-chains are beta(S) and the ratio of alpha(H)- to beta(S)-globin was 0.73. Introduction of a heterozygous mouse alpha-globin deletion into mice homozygous for the beta(major) deletion (alpha(H)beta(S)[alpha(MD)beta(MDD)]) resulted in 65.1 +/- 8.5% beta(S) and a human alpha/beta ratio of 0.89 +/- 0.2. Sickling occurs in 95% of erythrocytes from alpha(H)beta(S)[beta(MDD)] mice after slow deoxygenation. Transmission electron microscopy revealed polymer fiber formation but not fascicles of fiber. Increased organ weight was noted in lung, spleen, and kidney of transgenic mice vs. controls that may be due to hypertrophy or increased blood volume in the lungs and/or increased tissue water content. The hemoglobin content of lung, spleen, and kidney was also elevated in transgenic animals due to trapped hemoglobin and/or increased blood volume. When transgenic and control mice were examined by magnetic resonance imaging at 9.4 tesla, some transgenic animals had enlarged kidneys with prolonged relaxation time, consistent with increased organ weight and water content. The glomerular filtration rate was elevated in transgenic animals, which is characteristic of young sickle cell patients. Furthermore, exposure to hypoxia resulted in significantly decreased hematocrit, increased erythrocyte density, and induced a urine-concentrating defect. We conclude that the transgenic mouse line reported here has chronic organ damage and further hematological and organ dysfunction can be induced by hypoxia.
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页码:12155 / 12159
页数:5
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