Acute expression of the PRL receptor gene after ovariectomy in midpregnant mouse mammary gland

被引:13
作者
Mizoguchi, Y
Kim, JY
Sasaki, T
Hama, T
Sasaki, M
Enami, J
Sakai, S
机构
[1] UNIV TOKYO, FAC AGR, DEPT ANIM BREEDING, BUNKYO KU, TOKYO 113, JAPAN
[2] ZENYAYU KOGYO CO LTD, RES LAB, TOKYO 178, JAPAN
关键词
casein mRNA; lactogenesis; mammary gland; PRL receptor mRNA;
D O I
10.1507/endocrj.43.537
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In order to examine the time-dependent expression of the PRL receptor (PRL-R) gene at lactogenesis, the level of PRL-R mRNA was determined following ovariectomy in pregnant mouse mammary gland. Following reverse transcription, the quantity of mRNA was measured by the competitive polymerase chain reaction. The casein (a 22000 molecular weight component) mRNA level was measured as a marker for milk synthesis. Following ovariectomy, the onset of abortion occurred mostly at 22-23 h and the level of casein mRNA began to increase at 12 h. The long and short forms of PRL-R mRNAs were detected in a molar ratio of 1:0.2 on day 12 of pregnancy. Eight h after ovariectomy, the long form of PRL-R mRNA began to increase, showing a bell-shaped profile with the highest peak at 16 h. The short form of PRL-R mRNA was at low levels and remained constant. The levels of the long form of PRL-R mRNA decreased similarly in the presence and absence of foster pups from 24 to 48 h. Conversely, casein mRNA were maintained at high levels by supplying foster pups. The level of the long form of PRL-R mRNA reached a maximum prior to abortion. The present experiments demonstrated that the acute expression of the PRL-R gene occurred in the mammary gland at lactogenesis.
引用
收藏
页码:537 / 544
页数:8
相关论文
共 37 条
[1]   MULTIPLE FORMS OF PROLACTIN RECEPTOR MESSENGER-RIBONUCLEIC-ACID ARE SPECIFICALLY EXPRESSED AND REGULATED IN MURINE TISSUES AND THE MAMMARY CELL LINE-HC11 [J].
BUCK, K ;
VANEK, M ;
GRONER, B ;
BALL, RK .
ENDOCRINOLOGY, 1992, 130 (03) :1108-1114
[2]   MAMMARY GLUCOCORTICOID RECEPTOR OF MICE IN PREGNANCY AND IN LACTATION [J].
CHOMCZYNSKI, P ;
ZWIERZCHOWSKI, L .
BIOCHEMICAL JOURNAL, 1976, 158 (02) :481-483
[3]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[4]   ISOLATION, PURIFICATION, AND CHARACTERIZATION OF MOUSE PLACENTAL-LACTOGEN [J].
COLOSI, P ;
MARR, G ;
LOPEZ, J ;
HARO, L ;
OGREN, L ;
TALAMANTES, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (03) :771-775
[5]   EXPRESSION OF MULTIPLE FORMS OF THE PROLACTIN RECEPTOR IN MOUSE-LIVER [J].
DAVIS, JA ;
LINZER, DIH .
MOLECULAR ENDOCRINOLOGY, 1989, 3 (04) :674-680
[6]  
DAVIS JA, 1993, ENDOCRINOLOGY, V133, P224
[7]   EVOLUTION OF PROLACTIN RECEPTORS IN RABBIT MAMMARY-GLAND DURING PREGNANCY AND LACTATION [J].
DJIANE, J ;
DURAND, P ;
KELLY, PA .
ENDOCRINOLOGY, 1977, 100 (05) :1348-1356
[8]   PROLACTIN RECEPTOR GENE-EXPRESSION IN THE RABBIT - IDENTIFICATION, CHARACTERIZATION AND TISSUE DISTRIBUTION OF SEVERAL PROLACTIN RECEPTOR MESSENGER-RNAS ENCODING A UNIQUE PRECURSOR [J].
DUSANTERFOURT, I ;
GAYE, P ;
BELAIR, L ;
PETRIDOU, B ;
KELLY, PA ;
DJIANE, J .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1991, 77 (1-3) :181-192
[9]   IDENTIFICATION AND SEQUENCE-ANALYSIS OF A 2ND FORM OF PROLACTIN RECEPTOR BY MOLECULAR-CLONING OF COMPLEMENTARY-DNA FROM RABBIT MAMMARY-GLAND [J].
EDERY, M ;
JOLICOEUR, C ;
LEVIMEYRUEIS, C ;
DUSANTERFOURT, I ;
PETRIDOU, B ;
BOUTIN, JM ;
LESUEUR, L ;
KELLY, PA ;
DJIANE, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (06) :2112-2116
[10]   ANALYSIS OF CYTOKINE MESSENGER-RNA AND DNA - DETECTION AND QUANTITATION BY COMPETITIVE POLYMERASE CHAIN-REACTION [J].
GILLILAND, G ;
PERRIN, S ;
BLANCHARD, K ;
BUNN, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) :2725-2729