Lactoferrin is an estrogen responsive protein in the uterus of mice and rats

被引:21
作者
Jefferson, WN [1 ]
Padilla-Banks, E [1 ]
Newbold, RR [1 ]
机构
[1] NIEHS, Div Intramural Res, Environm Toxicol Program,Dev Endocrinol Sect, Lab Toxicol,Reprod Toxicol Grp,NIH, Res Triangle Pk, NC 27709 USA
关键词
estrogens; environmental estrogens; uterotrophic bioassay; marker proteins; lactoferrin; complement C3;
D O I
10.1016/S0890-6238(00)00061-7
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
To identify lactoferrin (LF) and determine its estrogen-responsiveness in the rat uterus, immature Sprague-Dawley rats were untreated or subcutaneously injected with 17 beta-estradiol (500 mu g/kg) for 3 days and uterine tissues collected. Outbred immature CD-1 mice, treated with 17 beta-estradiol, provided the positive control. By using a polyclonal antibody raised against mouse LF, minimal detectable protein was immunolocalized in uterine epithelial cells of untreated immature rats and mice. After estrogen treatment, LF was localized in all uterine epithelial cells of both species, although staining was more intense in mice than rats. In mice, LF was evenly distributed throughout the cytoplasm with intense staining in some cells, while in rats, it was seen mainly in the apical cytoplasm. For comparison to another well-known estrogen responsive protein in rats, complement C3 was immunolocalized within epithelial cells and it showed a different staining pattern than LF. Uterine tissue homogenates were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blots showed cross-reactivity with the mouse LF antibody. These findings indicate that LF is present in the rat uterus, and is induced by estrogens as reported in other species. Thus, LF is an important marker of estrogenic activity across species and will, therefore, have utility in screening for effects of environmental estrogenic compounds. Published by Elsevier Science Inc.
引用
收藏
页码:103 / 110
页数:8
相关论文
共 40 条
[11]   Methodologies for isolating estrogen-responsive proteins as markers of environmental toxicants [J].
Jefferson, WN ;
Teng, C ;
Newbold, RR .
TOXICOLOGY METHODS, 1996, 6 (04) :183-192
[12]  
JEFFERSON WN, 1996, CELL VISION, V3, P329
[13]  
Kelver ME, 1996, AM J REPROD IMMUNOL, V36, P243
[14]   ELECTROBLOTTING OF MULTIPLE GELS - A SIMPLE APPARATUS WITHOUT BUFFER TANK FOR RAPID TRANSFER OF PROTEINS FROM POLYACRYLAMIDE TO NITROCELLULOSE [J].
KYHSEANDERSEN, J .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1984, 10 (3-4) :203-209
[15]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[16]  
LI L, 1987, CANCER RES, V47, P4184
[17]   Various forms of mouse lactoferrins: purification and characterization [J].
Li, SH ;
Chen, YH .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1999, 726 (1-2) :45-52
[18]  
LIU YH, 1991, J BIOL CHEM, V266, P21880
[19]   LACTOFERRIN IN THE MOUSE UTERUS - ANALYSES OF THE PREIMPLANTATION PERIOD AND REGULATION BY OVARIAN-STEROIDS [J].
MCMASTER, MT ;
TENG, CT ;
DEY, SK ;
ANDREWS, GK .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (01) :101-111
[20]   Ontogeny of lactoferrin in the developing mouse uterus: A marker of early hormone response [J].
Newbold, RR ;
Hanson, RB ;
Jefferson, WN .
BIOLOGY OF REPRODUCTION, 1997, 56 (05) :1147-1157