Calreticulin:: An intracellular Ca++-binding protein abundantly expressed and regulated by androgen in prostatic epithelial cells

被引:37
作者
Zhu, N
Pewitt, EB
Cai, XY
Cohn, EB
Lang, S
Chen, R
Wang, Z
机构
[1] Northwestern Univ, Sch Med, Dept Urol, Chicago, IL 60611 USA
[2] Northwestern Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Chicago, IL 60611 USA
关键词
D O I
10.1210/en.139.10.4337
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Calreticulin was identified in a screen for androgen-response genes in the rat Ventral prostate. Northern blot and Western blot analyses in the rat model showed that both calreticulin messenger RNA and protein are down-regulated by castration and up-regulated by androgen replacement in the prostate. Northern blot analysis showed that calreticulin expression level in the prostate is much higher than that in seminal vesicles, heart, brain, muscle, kidney, and liver. The regulation of calreticulin expression by androgen is only observed in the prostate and seminal vesicles, two male secondary sex organs. The induction of calreticulin by androgen in prostate organ culture partially resists protein synthesis inhibition, suggesting that calreticulin is a direct androgen-response gene. In situ hybridization and immunohistochemistry studies showed that calreticulin is an intracellular protein in prostatic epithelial cells. Because calreticulin is a major intracellular Ca++-binding protein with 1 high-affinity and 25 low-affinity Ca++ binding sites, our observations suggest that calreticulin is a promising candidate that mediates androgen regulation of intracellular Ca++ levels and/or signals in prostatic epithelial cells. The expression of calreticulin is also regulated by androgen in the mouse and human prostate, suggesting that androgen regulation and function of calreticulin in the prostate are conserved evolutionarily.
引用
收藏
页码:4337 / 4344
页数:8
相关论文
共 34 条
  • [1] OVEREXPRESSION OF CALRETICULIN INCREASES THE CA2+ CAPACITY OF RAPIDLY EXCHANGING CA2+ STORES AND REVEALS ASPECTS OF THEIR LUMENAL MICROENVIRONMENT AND FUNCTION
    BASTIANUTTO, C
    CLEMENTI, E
    CODAZZI, F
    PODINI, P
    DEGIORGI, F
    RIZZUTO, R
    MELDOLESI, J
    POZZAN, T
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 130 (04) : 847 - 855
  • [2] Bleackley R C, 1995, Curr Top Microbiol Immunol, V198, P145
  • [3] BOLLAG DM, 1991, PROTEIN METHODS, P181
  • [4] Bruchovsky N, 1975, Vitam Horm, V33, P61
  • [5] Bruchovsky N, 1996, PROSTATE, P13
  • [6] CALRETICULIN INHIBITS REPETITIVE INTRACELLULAR CA2+ WAVES
    CAMACHO, P
    LECHLEITER, JD
    [J]. CELL, 1995, 82 (05) : 765 - 771
  • [7] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [8] POLYMERIZATION OF DEOXYRIBONUCLEOTIDES IN RELATION TO ANDROGEN-INDUCED PROSTATIC GROWTH
    COFFEY, DS
    SHIMAZAKI, J
    WILLIAMS.HG
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1968, 124 (1-3) : 184 - +
  • [9] CALCIUM-CHANNEL ANTAGONISTS DELAY REGRESSION OF ANDROGEN-DEPENDENT TISSUES AND SUPPRESS GENE ACTIVITY ASSOCIATED WITH CELL-DEATH
    CONNOR, J
    SAWCZUK, IS
    BENSON, MC
    TOMASHEFSKY, P
    OTOOLE, KM
    OLSSON, CA
    BUTTYAN, R
    [J]. PROSTATE, 1988, 13 (02) : 119 - 130
  • [10] Calreticulin is essential for integrin-mediated calcium signalling and cell adhesion
    Coppolino, MG
    Woodside, MJ
    Demaurex, N
    Grinstein, S
    StArnaud, R
    Dedhar, S
    [J]. NATURE, 1997, 386 (6627) : 843 - 847