Human androgen deficiency: insights gained from androgen receptor knockout mouse models

被引:57
作者
Rana, Kesha [1 ]
Davey, Rachel A. [1 ]
Zajac, Jeffrey D. [1 ]
机构
[1] Univ Melbourne, Austin Hlth, Dept Med, Heidelberg, Vic, Australia
关键词
androgen receptor; androgen receptor knockout mouse model; androgen deficiency; PROSTATE EPITHELIAL DEVELOPMENT; MICE LACKING; MUSCLE STRENGTH; INSULIN-RESISTANCE; BODY-COMPOSITION; BONE-RESORPTION; TESTOSTERONE REPLACEMENT; SEX-DIFFERENCES; ADIPOSE-TISSUE; YOUNG MEN;
D O I
10.4103/1008-682X.122590
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
The mechanism of androgen action is complex. Recently, significant advances have been made into our understanding of how androgens act via the androgen receptor (AR) through the use of genetically modified mouse models. A number of global and tissue-specific AR knockout (ARKO) models have been generated using the Cre-loxP system which allows tissue- and/or cell-specific deletion. These ARKO models have examined a number of sites of androgen action including the cardiovascular system, the immune and hemopoetic system, bone, muscle, adipose tissue, the prostate and the brain. This review focuses on the insights that have been gained into human androgen deficiency through the use of ARKO mouse models at each of these sites of action, and highlights the strengths and limitations of these Cre-loxP mouse models that should be considered to ensure accurate interpretation of the phenotype.
引用
收藏
页码:169 / 177
页数:9
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