Expression of a renin/GFP transgene in mouse embryonic, extra-embryonic, and adult tissues

被引:62
作者
Jones, CA
Hurley, MI
Black, TA
Kane, CM
Pan, L
Pruitt, SC
Gross, KW
机构
[1] Roswell Pk Canc Inst, Dept Mol & Cellular Biol, Buffalo, NY 14263 USA
[2] Dyouville Coll, Dept Math & Nat Sci, Buffalo, NY 14201 USA
关键词
reporter gene; green fluorescent protein; giant cell trophoblast; juxtaglomerular cells; placenta;
D O I
10.1152/physiolgenomics.2000.4.1.75
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A reporter construct was assembled with 4-kb of renin 5'-flanking sequence fused to humanized green fluorescent protein (GFP) cDNA. Transgenic mice carrying this construct were produced and assayed for GFP expression. In the adult, expression was detected in juxtaglomerular (JG) cells of the kidney and granular convoluted tubular cells of the submandibular gland. Furthermore, treatment of mice with captopril induced GFP expression in renal vascular smooth muscle cells. During embryogenesis, GFP expression was first detected at embryonic day E13 in the adrenal gland and Wolffian duct. Expression was also seen in the developing renal vasculature as early as E14 and remained detectable through birth. Renal GFP expression became restricted to JG cells in adults. Fetal adrenal and gonadal arteries also expressed GFP. In the placenta, GFP was observed in giant cell trophoblasts, consistent with reports of renin expression in chorionic cells of both humans and mice. We conclude that 4 kb of renin 5' flank is sufficient to direct multiple known renin expression patterns. Furthermore, the renin-GFP construct characterized here will provide a useful vital reporter for renin expression.
引用
收藏
页码:75 / 81
页数:7
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