ACTIVATION OF MAP KINASE ASSOCIATED WITH THE PRIMING EFFECT OF LHRH

被引:59
作者
MITCHELL, R
SIM, PJ
LESLIE, T
JOHNSON, MS
THOMSON, FJ
机构
[1] MRC Brain Metabolism Unit, Edinburgh EH8 9JZ
关键词
D O I
10.1677/joe.0.140R015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A MAP kinase activity assay was developed to determine whether the LHRH receptor could activate this enzyme (particularly during LHRH priming). In anterior pituitary tissue from pro-oestrous rats LHRH caused concentration-dependent activation of MAP kinase after 5-10 min and continued for up to 60 min of incubation. The magnitude of this response correlated with that of LHRH priming on various days of the oestrous cycle but not with the magnitude of 1st hour (unprimed) LHRH-induced LH release. The response to LHRH was mimicked by a phorbol ester but not by ionomycin and was blocked with high potency by GF 109203X but not by H7 (in a similar manner to the PKC species that mediates LHRH priming). Neither the tyrosine kinase inhibitor lavendustin A nor the protein synthesis inhibitor cycloheximide blocked LHRH-induced MAP kinase activation. The possible functional significance of MAP kinase activation in gonadotrophs is considered with respect to LHRH priming.
引用
收藏
页码:R15 / R18
页数:4
相关论文
共 32 条
[1]  
ALVAREZ E, 1991, J BIOL CHEM, V266, P15277
[2]  
CLARKLEWIS I, 1991, J BIOL CHEM, V266, P15180
[3]   EXTRACELLULAR SIGNAL-REGULATED KINASES - ERKS IN PROGRESS [J].
COBB, MH ;
BOULTON, TG ;
ROBBINS, DJ .
CELL REGULATION, 1991, 2 (12) :965-978
[4]   ACTIVATION OF MITOGEN-ACTIVATED PROTEIN-KINASE KINASE BY V-RAF IN NIH 3T3 CELLS AND INVITRO [J].
DENT, P ;
HASER, W ;
HAYSTEAD, TAJ ;
VINCENT, LA ;
ROBERTS, TM ;
STURGILL, TW .
SCIENCE, 1992, 257 (5075) :1404-1407
[5]   A 42-KD TYROSINE KINASE SUBSTRATE LINKED TO CHROMAFFIN CELL SECRETION EXHIBITS AN ASSOCIATED MAP KINASE-ACTIVITY AND IS HIGHLY RELATED TO A 42-KD MITOGEN-STIMULATED PROTEIN IN FIBROBLASTS [J].
ELY, CM ;
ODDIE, KM ;
LITZ, JS ;
ROSSOMANDO, AJ ;
KANNER, SB ;
STURGILL, TW ;
PARSONS, SJ .
JOURNAL OF CELL BIOLOGY, 1990, 110 (03) :731-742
[6]  
Fink G., 1988, P1349
[7]   ISOQUINOLINESULFONAMIDES, NOVEL AND POTENT INHIBITORS OF CYCLIC-NUCLEOTIDE DEPENDENT PROTEIN-KINASE AND PROTEIN KINASE-C [J].
HIDAKA, H ;
INAGAKI, M ;
KAWAMOTO, S ;
SASAKI, Y .
BIOCHEMISTRY, 1984, 23 (21) :5036-5041
[8]   MITOGEN-ACTIVATED-PROTEIN-KINASE-CATALYZED PHOSPHORYLATION OF MICROTUBULE-ASSOCIATED PROTEINS, MICROTUBULE-ASSOCIATED PROTEIN-2 AND MICROTUBULE-ASSOCIATED PROTEIN-4, INDUCES AN ALTERATION IN THEIR FUNCTION [J].
HOSHI, M ;
OHTA, K ;
GOTOH, Y ;
MORI, A ;
MUROFUSHI, H ;
SAKAI, H ;
NISHIDA, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 203 (1-2) :43-52
[9]  
HSU CYJ, 1991, J BIOL CHEM, V266, P21105
[10]   EVIDENCE FOR A DISTINCT H7-RESISTANT FORM OF PROTEIN-KINASE-C IN RAT ANTERIOR-PITUITARY GLAND [J].
ISON, AJ ;
MACEWAN, DJ ;
JOHNSON, MS ;
CLEGG, RA ;
CONNOR, K ;
MITCHELL, R .
FEBS LETTERS, 1993, 329 (1-2) :199-204