Localization and regulation of the growth hormone receptor and growth hormone-binding protein in the rat growth plate

被引:45
作者
Gevers, EF
Van Der Eerden, BCJ
Karperien, M
Raap, AK
Robinson, ICAF
Wit, JM
机构
[1] Natl Inst Med Res, Div Mol Neuroendocrinol, London NW7 1AA, England
[2] Leiden Univ, Ctr Med, Dept Pediat, Leiden, Netherlands
[3] Leiden Univ, Ctr Med, Dept Endocrinol & Metab Dis, Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Dept Mol Cell Biol, Lab Cytochem & Cytol, Leiden, Netherlands
关键词
growth plate; chondrocyte; growth hormone receptor; growth hormone binding protein; tyramide signal amplification;
D O I
10.1359/jbmr.2002.17.8.1408
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Growth hormone (GH) has direct effects on the growth plate to stimulate longitudinal growth, but it is not clear which chondrocyte populations GH acts on. The dual effector theory suggests that GH would act primarily on the "stem cells." However, staining with a GH receptor (GHR) antibody is found in all layers of the growth plate in rabbits and humans. We now have investigated the localization and regulation of GHR and the related GH binding protein (GHBP) in the rat growth plate using a sensitive immunohistochemical method involving tyramide signal amplification (TSA) and antibodies specific for GHR or GHBP. Both GHR and GHBP were shown in the germinal and proliferative chondrocytes, but most clearly in early maturing chondrocytes at the interface between proliferative and hypertrophic cells. Staining for GHR and GHBP was located in both the cytoplasm and the nucleus. Expression of GHR mRNA and GHBP mRNA in the growth plate was confirmed by reverse-transcription polymerase chain reaction (RT-PCR). Immunohistochemical staining for GHR and GHBP decreased with age; in 12-week-old normal rats, only the early maturing chondrocytes were stained. In GH-deficient dwarf rats, staining seemed less than in normal rats, and in hypophysectomized (Hx) rats, staining for GHBP was clearly reduced. Treatment of Hx rats with thyroid hormones (T-3 + T-4), via subcutaneously (sc) implanted osmotic minipumps, induced little growth and induced a small layer of GHR-positive and GHBP-positive early maturing chondrocytes. Treatment with GH and thyroid hormones (TH) resulted in greater growth and a broader layer of GHR-positive and GHBP-positive cells, indistinguishable from normal rats. In contrast, dexamethasone treatment of normal rats inhibited their growth and reduced GHR and GHBP staining in the growth plate. These results show that GHR and GHBP in the growth plate are under hormonal control. The localization of GHR/GHBP suggests that in addition to actions on germinal and proliferative cells in young rats, GH also has effects on early maturing chondrocytes and may be involved in their differentiation to a fully hypertrophic chondrocyte.
引用
收藏
页码:1408 / 1419
页数:12
相关论文
共 64 条
  • [51] Effect of growth hormone and insulin-like growth factor I (IGF-I) on the expression of IGF-I messenger ribonucleic acid and peptide in rat tibial growth plate and articular chondrocytes in vivo
    Reinecke, M
    Schmid, AC
    Heyberger-Meyer, B
    Hunziker, EB
    Zapf, J
    [J]. ENDOCRINOLOGY, 2000, 141 (08) : 2847 - 2853
  • [52] ROBINSON I, 1993, INT J PAED S, V82, P22
  • [53] Truncated growth hormone receptor isoforms
    Ross, RJM
    [J]. ACTA PAEDIATRICA, 1999, 88 : 164 - 166
  • [54] IDENTIFICATION OF THE ORIGIN OF THE GROWTH HORMONE-BINDING PROTEIN IN RAT SERUM
    SADEGHI, H
    WANG, BS
    LUMANGLAS, AL
    LOGAN, JS
    BAUMBACH, WR
    [J]. MOLECULAR ENDOCRINOLOGY, 1990, 4 (12) : 1799 - 1805
  • [55] Bone homeostasis in growth hormone receptor-null mice is restored by IGF-I but independent of Stat5
    Sims, NA
    Clément-Lacroix, P
    Da Ponte, F
    Bouali, Y
    Binart, N
    Moriggl, R
    Goffin, V
    Coschigano, K
    Gaillard-Kelly, M
    Kopchick, J
    Baron, R
    Kelly, PA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (09) : 1095 - 1103
  • [56] Liver-derived insulin-like growth factor I (IGF-I) is the principal source of IGF-I in blood but is not required for postnatal body growth in mice
    Sjögren, K
    Liu, JL
    Blad, K
    Skrtic, S
    Vidal, O
    Wallenius, V
    LeRoith, D
    Törnell, J
    Isaksson, OGP
    Jansson, JO
    Ohlsson, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) : 7088 - 7092
  • [57] PASSIVE-IMMUNIZATION AGAINST INSULIN-LIKE GROWTH FACTOR-I DOES NOT INHIBIT GROWTH HORMONE-STIMULATED GROWTH OF DWARF RATS
    SPENCER, GSG
    HODGKINSON, SC
    BASS, JJ
    [J]. ENDOCRINOLOGY, 1991, 128 (04) : 2103 - 2109
  • [58] TISSUE DISTRIBUTION, CHARACTERIZATION, AND REGULATION OF MESSENGER-RIBONUCLEIC-ACID FOR GROWTH-HORMONE RECEPTOR AND SERUM BINDING-PROTEIN IN THE RAT
    TIONG, TS
    HERINGTON, AC
    [J]. ENDOCRINOLOGY, 1991, 129 (03) : 1628 - 1634
  • [59] Expression of Indian hedgehog, parathyroid hormone-related protein, and their receptors in the postnatal growth plate of the rat: Evidence for a locally acting growth restraining feedback loop after birth
    Van Der Eerden, BCJ
    Karperien, M
    Gevers, EF
    Lowik, CWGM
    Wit, JM
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (06) : 1045 - 1055
  • [60] The CCAAT/enhancer-binding protein-alpha is expressed in the germinal layer of the growth plate: colocalisation with the growth hormone receptor
    Vidal, NOA
    Ekberg, S
    Enerback, S
    Lindahl, A
    Ohlsson, C
    [J]. JOURNAL OF ENDOCRINOLOGY, 1997, 155 (03) : 433 - 441