Gene expression of catecholamine synthesizing enzymes and beta adrenoceptor subtypes during rat embryogenesis

被引:27
作者
Fujinaga, M
Scott, JC
机构
[1] STANFORD UNIV, SCH MED, DEPT ANESTHESIA, STANFORD, CA 94305 USA
[2] VA PALO ALTO HLTH CARE SYST, ANESTHESIOL SERV, PALO ALTO, CA 94304 USA
[3] UNIV NEW MEXICO, SCH MED, DEPT ANESTHESIOL, ALBUQUERQUE, NM 87131 USA
关键词
catecholamines; catecholamine synthesizing enzyme; beta adrenoceptor; embryogenesis; rat;
D O I
10.1016/S0304-3940(97)00511-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Timed-pregnant Sprague-Dawley rats were killed between gestational day (GD) 8 and 10, and embryos were explanted and separated into developmental stages according to a modified Theiler's system. Total RNA from each stage was isolated and subjected to reverse transcription-polymerase chain reaction (RT-PCR) assays to examine gene expression of catecholamine synthesizing enzymes and three subtypes of beta adrenoceptors. Expression of these genes was detected at much earlier stages than previously reported, and each enzyme and receptor subtype showed a different pattern of gene expression. For example, mRNA for tyrosine hydroxylase, the rate-limiting enzyme for catecholamine synthesis, was detected as early as stage 10a, late GD 8, before the neural crest cells appear (stage 12, mid GD 10). This contradicts the common belief that catecholamines are produced only in the cells of sympathoadrenal lineage which originate from the neural crest cells and the cells of central nervous system. Results from the present study indicate that catecholamine synthesis is not limited to the cells of sympathoadrenal lineage. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:108 / 112
页数:5
相关论文
共 25 条
[11]  
KAUFMAN MH, 1981, J ANAT, V133, P235
[12]  
KIRBY ML, 1972, ANAT REC, V173, P469
[13]   WHOLE EMBRYO CULTURE - INTERPRETATION OF ABNORMAL-DEVELOPMENT INVITRO [J].
KLUG, S .
REPRODUCTIVE TOXICOLOGY, 1991, 5 (03) :237-244
[14]   TARGETED DISRUPTION OF THE TYROSINE-HYDROXYLASE LOCUS RESULTS IN SEVERE CATECHOLAMINE DEPLETION AND PERINATAL LETHALITY IN MICE [J].
KOBAYASHI, K ;
MORITA, S ;
SAWADA, H ;
MIZUGUCHI, T ;
YAMADA, K ;
NAGATSU, I ;
HATA, T ;
WATANABE, Y ;
FUJITA, K ;
NAGATSU, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :27235-27243
[15]   BETA-ADRENERGIC STIMULATION OF GROWTH-HORMONE (GH) RELEASE INVIVO, AND SUBSEQUENT INHIBITION OF GH-RELEASING FACTOR-INDUCED GH SECRETION [J].
KRIEG, RJ ;
PERKINS, SN ;
JOHNSON, JH ;
ROGERS, JP ;
ARIMURA, A ;
CRONIN, MJ .
ENDOCRINOLOGY, 1988, 122 (02) :531-537
[16]   CATECHOLAMINES AND MORPHOGENESIS OF CHICK NEURAL TUBE AND NOTOCHORD [J].
LAWRENCE, IE ;
BURDEN, HW .
AMERICAN JOURNAL OF ANATOMY, 1973, 137 (02) :199-207
[17]   CARDIAC PACEMAKING - OBLIGATORY ROLE OF CATECHOLAMINES [J].
POLLACK, GH .
SCIENCE, 1977, 196 (4291) :731-738
[18]   DOPAMINE BETA-HYDROXYLASE DEFICIENCY - A GENETIC DISORDER OF CARDIOVASCULAR REGULATION [J].
ROBERTSON, D ;
HAILE, V ;
PERRY, SE ;
ROBERTSON, RM ;
PHILLIPS, JA ;
BIAGGIONI, I .
HYPERTENSION, 1991, 18 (01) :1-8
[19]   Targeted disruption of the mouse beta 1-adrenergic receptor gene: Developmental and cardiovascular effects [J].
Rohrer, DK ;
Desai, KH ;
Jasper, JR ;
Stevens, ME ;
Regula, DP ;
Barsh, GS ;
Bernstein, D ;
Kobilka, BK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7375-7380
[20]   CATECHOLAMINES IN THE YOLK-SAC EPITHELIUM OF THE RAT [J].
SCHLUMPF, M ;
LICHTENSTEIGER, W .
ANATOMY AND EMBRYOLOGY, 1979, 156 (02) :177-187