[2] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[3] Univ Calif San Diego, Dept Pharmacol, San Diego, CA USA
[4] Vet Adm Med Ctr, San Diego, CA 92161 USA
来源:
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
|
2005年
/
16卷
/
11期
关键词:
D O I:
10.1681/ASN.2005040450
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
The use of gene-modified mouse models allows the experimental in vivo analysis of specific gene defects at the level of target cells. With respect to the epithelial sodium channel and some of its regulatory proteins, gene-modified models that control gene defects in a time- and tissue-dependent conditional or constitutive manner have been generated. The combination of molecular and physiologic approaches in these mouse models increases the understanding of the complex regulation and the cell signaling cascades involved in Na+ transport in target cells and may ultimately provide new insights into the pathophysiology of renal Na+ retention and BP regulation. This review summarizes and discusses the gene-targeting approaches that have been applied to the epithelial sodium channel and its regulatory proteins.
引用
收藏
页码:3160 / 3166
页数:7
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[41]
Vuagniaux G, 2000, J AM SOC NEPHROL, V11, P828, DOI 10.1681/ASN.V115828