α1-Adrenoceptor subtypes differentially couple to growth promotion and inhibition in Chinese hamster ovary cells

被引:46
作者
Keffel, S
Alexandrov, A
Goepel, M
Michel, MC
机构
[1] Univ Essen Gesamthsch, Dept Med, D-4300 Essen, Germany
[2] Univ Essen Gesamthsch, Dept Urol, Essen, Germany
关键词
D O I
10.1006/bbrc.2000.2850
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
We have compared the coupling of human alpha(1A)-, alpha(1B)-, and alpha(1D)-adrenoceptors (expressed at approximate to 2000 fmol/mg protein in Chinese hamster ovary cells) to cellular growth promotion (as assessed by [H-3]thymidine incorporation) and related signaling mechanisms. Maximum elevation of intracellular Ca2+ by the three subtypes occurred with the rank order a, (1691 nM) > alpha(1D) (1215 nM) > alpha(1B), (360 nM). In contrast, activation of the ERK, JNK, and p38 forms of mitogen-activated protein kinases occurred with the rank order alpha(1D) > alpha(1A), > alpha(1B). alpha(1A)-Adrenoceptor stimulation inhibited basal and growth factor-stimulated [H-3]thymidine incorporation by 74%, and this was mitigated by p38 inhibition. In contrast, alpha(1D)-adrenoceptor stimulation enhanced cellular growth by 136%, and this was blocked by two distinct inhibitors of ERK activation. We conclude that within a given cell type alpha(1)-adrenoceptor subtypes can have opposite effects on cellular growth, although their proximal signal transduction displays only quantitative differences. (C) 2000 Academic Press.
引用
收藏
页码:906 / 911
页数:6
相关论文
共 33 条
  • [1] PD-098059 IS A SPECIFIC INHIBITOR OF THE ACTIVATION OF MITOGEN-ACTIVATED PROTEIN-KINASE KINASE IN-VITRO AND IN-VIVO
    ALESSI, DR
    CUENDA, A
    COHEN, P
    DUDLEY, DT
    SALTIEL, AR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) : 27489 - 27494
  • [2] Stimulation of α1A-adrenoceptors in rat-1 cells inhibits extracellular signal-regulated kinase by activating p38 mitogen-activated protein kinase
    Alexandrov, A
    Keffel, S
    Goepel, M
    Michel, MC
    [J]. MOLECULAR PHARMACOLOGY, 1998, 54 (05) : 755 - 760
  • [3] Differential regulation of 46 and 54 kDa jun N-terminal kinases and p38 mitogen-activated protein kinase by human α1A-adrenoceptors expressed in rat-1 cells
    Alexandrov, A
    Keffel, S
    Goepel, M
    Michel, MC
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 261 (02) : 372 - 376
  • [4] ANZUKHOVSKY EP, 1994, CIRC RES, V74, P937
  • [5] Selective activation of α1A-adrenergic receptors in neonatal cardiac myocytes is sufficient to cause hypertrophy and differential regulation of α1-adrenergic receptor subtype mRNAs
    Autelitano, DJ
    Woodcock, EA
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1998, 30 (08) : 1515 - 1523
  • [6] BALBOA MA, 1994, J BIOL CHEM, V269, P10511
  • [7] No role for Ca++ or protein kinase C in alpha-1A adrenergic receptor activation of mitogen-activated protein kinase pathways in transfected PC12 cells
    Berts, A
    Zhong, HY
    Minneman, KP
    [J]. MOLECULAR PHARMACOLOGY, 1999, 55 (02) : 296 - 303
  • [8] Adrenergic receptor stimulation of the mitogen-activated protein kinase cascade and cardiac hypertrophy
    Bogoyevitch, MA
    Andersson, MB
    GillespieBrown, J
    Clerk, A
    Glennon, PE
    Fuller, SJ
    Sugden, PH
    [J]. BIOCHEMICAL JOURNAL, 1996, 314 : 115 - 121
  • [9] BYLUND DB, 1994, PHARMACOL REV, V46, P121
  • [10] SPECIFIC ALPHA-1-ADRENERGIC RECEPTOR SUBTYPES MODULATE CATECHOLAMINE-INDUCED INCREASES AND DECREASES IN VENTRICULAR AUTOMATICITY
    DELBALZO, U
    ROSEN, MR
    MALFATTO, G
    KAPLAN, LM
    STEINBERG, SF
    [J]. CIRCULATION RESEARCH, 1990, 67 (06) : 1535 - 1551