EXPRESSION AND AGONIST-INDUCED DOWN-REGULATION OF MESSENGER-RNAS OF M2-MUSCARINIC AND M3-MUSCARINIC ACETYLCHOLINE-RECEPTORS IN CULTURED CEREBELLAR GRANULE CELLS

被引:64
作者
FUKAMAUCHI, F [1 ]
HOUGH, C [1 ]
CHUANG, DM [1 ]
机构
[1] NIMH,BIOL PSYCHIAT BRANCH,MOLEC NEUROBIOL,BLDG 10,ROOM 3N-212,BETHESDA,MD 20892
关键词
MUSCARINIC RECEPTOR MESSENGER RNA; DESENSITIZATION; CEREBELLAR GRANULE CELLS;
D O I
10.1111/j.1471-4159.1991.tb08210.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The regulation and expression of muscarinic acetylcholine receptor (mAChR) mRNA was studied in cultured cerebellar granule cells using Northern blot hybridization. mRNA species for m2- and m3-mAChRs but not m1- and m4-mAChRs were detected in these cells. The expression of mRNAs of both m2- and m3-mAChRs reached a maximum on the tenth day in culture but their expression patterns differed. Treatment of cerebellar granule cells after 8 days in culture with 100-mu-M carbachol led to differential down-regulation of the mRNA species of both mAChR subtypes present. Muscarinic receptor antagonists, atropine (1-mu-M) and pirenzepine (10-mu-M), prevented carbachol-induced m3-mAChR mRNA down-regulation observed at 8 h. However, exposure to either atropine or pirenzepine alone for 8 h led to a significant up-regulation of m3-mAChR mRNA. Thus, the mRNA species for both m2- and m3-mAChR subtypes are differentially expressed in culture and down-regulated by agonist stimulation. The loss of these mRNA species may play a role in the down-regulation of mAChR binding sites that occurs after desensitization.
引用
收藏
页码:716 / 719
页数:4
相关论文
共 15 条
[1]   THE MOLECULAR-BASIS OF MUSCARINIC RECEPTOR DIVERSITY [J].
BONNER, TI .
TRENDS IN NEUROSCIENCES, 1989, 12 (04) :148-151
[2]   CLONING AND EXPRESSION OF THE HUMAN AND RAT M5 MUSCARINIC ACETYLCHOLINE-RECEPTOR GENES [J].
BONNER, TI ;
YOUNG, AC ;
BRANN, MR ;
BUCKLEY, NJ .
NEURON, 1988, 1 (05) :403-410
[3]  
BUCKLEY NJ, 1988, J NEUROSCI, V8, P4646
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]  
CHUANG D-M, 1989, Society for Neuroscience Abstracts, V15, P974
[6]   NUMBER AND EVOLUTIONARY CONSERVATION OF ALPHA-TUBULIN AND BETA-TUBULIN AND CYTOPLASMIC BETA-ACTIN AND GAMMA-ACTIN GENES USING SPECIFIC CLONED CDNA PROBES [J].
CLEVELAND, DW ;
LOPATA, MA ;
MACDONALD, RJ ;
COWAN, NJ ;
RUTTER, WJ ;
KIRSCHNER, MW .
CELL, 1980, 20 (01) :95-105
[7]   HOMOLOGOUS DESENSITIZATION OF MUSCARINIC CHOLINERGIC, HISTAMINERGIC, ADRENERGIC, AND SEROTONERGIC RECEPTORS COUPLED TO PHOSPHOLIPASE-C IN CEREBELLAR GRANULE CELLS [J].
DILLONCARTER, O ;
CHUANG, DM .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (02) :598-603
[8]   SELECTIVE RELEASE OF GLUTAMATE FROM CEREBELLAR GRANULE CELLS DIFFERENTIATING IN CULTURE [J].
GALLO, V ;
CIOTTI, MT ;
COLETTI, A ;
ALOISI, F ;
LEVI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (24) :7919-7923
[9]   COMPARATIVE-STUDIES OF PHOSPHOINOSITIDE HYDROLYSIS INDUCED BY ENDOTHELIN-RELATED PEPTIDES IN CULTURED CEREBELLAR ASTROCYTES, C6-GLIOMA AND CEREBELLAR GRANULE CELLS [J].
LIN, WW ;
LEE, CY ;
CHUANG, DM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (02) :512-519
[10]   MOLECULAR PHARMACOLOGY OF MUSCARINIC RECEPTOR HETEROGENEITY [J].
MEI, L ;
ROESKE, WR ;
YAMAMURA, HI .
LIFE SCIENCES, 1989, 45 (20) :1831-1851