Distribution pattern of somatostatin and cortistatin mRNA in human central and peripheral tissues

被引:60
作者
Dalm, VASH
Van Hagen, PM
de Krijger, RR
Kros, JM
Van Koetsveld, PM
Van Der Lely, AJ
Lamberts, SWJ
Hofland, LJ
机构
[1] Erasmus MC, Dept Internal Med, Josephine Nefkens Inst, NL-3015 GD Rotterdam, Netherlands
[2] Erasmus MC, Dept Immunol, Josephine Nefkens Inst, NL-3015 GD Rotterdam, Netherlands
[3] Erasmus MC, Dept Pathol, Josephine Nefkens Inst, NL-3015 GD Rotterdam, Netherlands
关键词
D O I
10.1111/j.1365-2265.2004.02024.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Somatostatin receptors (sst) and their endogenous ligand, somatostatin (SS), are widely expressed throughout the human body. Recently, the cDNA of a novel SS-like peptide, named cortistatin (CST), has been cloned. This CST was found to be expressed in more restricted areas, like brain cortex, testes, kidney, stomach and leucocytes. Further studies demonstrated a selective expression of CST in tissues and cells of the human immune system, while SS was not expressed. OBJECTIVE In the present study we investigated the expression pattern of both SS mRNA and CST mRNA in various human central and peripheral tissues by quantitative RT-PCR (Q-PCR), in order to evaluate whether CST is more widely expressed in man than described to date and to investigate the relationship between SS and CST expression levels in various tissues. Previously, two different CST mRNA isoforms have been described. Therefore, we investigated the expression of both isoforms by RT-PCR in the different tissues as well. RESULTS We demonstrate for the first time that CST mRNA is widely expressed in the human body. Interestingly, a selective expression of CST mRNA and not SS mRNA was only found in isolated cells of the human immune system, whereas different tissues expressed both SS and CST mRNA. CONCLUSION CST may have a broader functional role than previously assumed.
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收藏
页码:625 / 629
页数:5
相关论文
共 29 条
  • [1] Somatostatin receptor subtype expression in human thyroid and thyroid carcinoma cell lines
    Ain, KB
    Taylor, KD
    Tofiq, S
    Venkataraman, G
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (06) : 1857 - 1862
  • [2] Gene expression profiling in the post-mortem human brain - no cause for dismay
    Bahn, S
    Augood, S
    Standaert, DG
    Starkey, M
    Emson, PC
    [J]. JOURNAL OF CHEMICAL NEUROANATOMY, 2001, 22 (1-2) : 79 - 94
  • [3] Segmental expression of somatostatin receptor subtypes sst1 and sst2 in tubules and glomeruli of human kidney
    Balster, DA
    O'Dorisio, MS
    Summers, MA
    Turman, MA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2001, 280 (03) : F457 - F465
  • [4] Evidence for a selective loss of somatostatin receptor subtype expression in male germ cell tumors of seminoma type
    Baou, N
    Bouras, M
    Droz, JP
    Benahmed, M
    Krantic, S
    [J]. CARCINOGENESIS, 2000, 21 (04) : 805 - 810
  • [5] SOMATOSTATIN - A PEPTIDE WITH UNEXPECTED PHYSIOLOGICAL ACTIVITIES
    BRAZEAU, P
    [J]. AMERICAN JOURNAL OF MEDICINE, 1986, 81 (6B) : 8 - 13
  • [6] Multiple regulation of adenylyl cyclase activity by G-protein coupled receptors in human foetal lung fibroblasts
    Busto, R
    Carrero, I
    Zapata, P
    Colás, B
    Prieto, JC
    [J]. REGULATORY PEPTIDES, 2000, 95 (1-3) : 53 - 58
  • [7] Identification of functional somatostatin receptors and G-proteins in a new line of human foetal lung fibroblasts
    Busto, R
    Carrero, I
    Zapata, P
    Colás, B
    Prieto, JC
    [J]. ENDOCRINE RESEARCH, 2000, 26 (03) : 477 - 486
  • [8] CHESSELET MF, 1995, CIBA F SYMP, V190, P51
  • [9] Cortistatin rather than somatostatin as a potential endogenous ligand for somatostatin receptors in the human immune system
    Dalm, VA
    van Hagen, PM
    van Koetsveld, PM
    Langerak, AW
    van der Lely, AJ
    Lamberts, SW
    Hofland, LJ
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (01) : 270 - 276
  • [10] Cloning, mRNA expression, and chromosomal mapping of mouse and human preprocortistatin
    deLecea, L
    RuizLozano, P
    Danielson, PE
    PeelleKirley, J
    Foye, PE
    Frankel, WN
    Sutcliffe, JG
    [J]. GENOMICS, 1997, 42 (03) : 499 - 506