Lazowski D A, Fraher L J, Hodsman A, Steer B, Modrowski D, Han V K
Department of Physical Therapy, University of Western Ontario, Lawson Research Institute, London, Ontario, Canada.
Bone. 1994 Sep-Oct;15(5):563-76. doi: 10.1016/8756-3282(94)90282-8.
Regulation of long bone growth by growth hormone and other endocrine factors is mediated by the local synthesis of IGF-I in the growth plate. Recent evidence suggests that different regions of the growth plate exhibit variable growth rates. To investigate whether IGF-I gene expression in the growth plate differs in relation to growth, we examined the distribution of IGF-I mRNA and peptide using in situ hybridization and immunohistochemistry, respectively, in the tibiae of 18-week-old rats (n = 6). Osteoblasts were identified by osteocalcin immunoreactivity, and osteoclasts by tartrate-resistant acid phosphatase (TRAP) histochemistry. The abundance of IGF-I mRNA in growth plate chondrocytes was quantified by counting the autoradiographic signal associated with each cell. IGF-I mRNA was identified in chondrocytes of both the proliferative and hypertrophic zones of the growth plate. Cells in the marginal regions of both zones contained significantly more IGF-I mRNA than those in the central region (p < 0.05). In addition, IGF-I mRNA levels were greater in the periphery of the growth plate on the medial side of the tibia (p < 0.05) in which there was more active growth than the lateral side. IGF-I immunoreactivity was present predominantly in the hypertrophic zone chondrocytes and no regional differences in its distribution were observed. IGF-I mRNA and peptide were also identified in periosteal fibroblasts, notably at sites of muscle attachment to bone, and in osteoblasts at active sites of bone remodelling in the periosteal, endocortical, and endosteal bone envelopes. In the TRAP-positive osteoclasts, IGF-I immunoreactivity, but not IGF-I mRNA, was detected. In addition, both IGF-I mRNA and peptide were identified in the hemopoietic cells of the metaphyseal bone marrow, whereas only IGF-I immunoreactivity was detectable in the diaphysis. We conclude that, in the tibiae of mature rats: (i) IGF-I gene expression in the growth plate is related to its growth and/or synthetic activity; and (ii) the presence of IGF-I in osteoblasts and osteoclasts suggests its involvement in active bone growth and remodeling.
生长激素和其他内分泌因子对长骨生长的调节是通过生长板中IGF-I的局部合成介导的。最近的证据表明,生长板的不同区域表现出不同的生长速率。为了研究生长板中IGF-I基因表达与生长的关系,我们分别使用原位杂交和免疫组织化学方法,检测了18周龄大鼠(n = 6)胫骨中IGF-I mRNA和肽的分布。通过骨钙素免疫反应性鉴定成骨细胞,通过抗酒石酸酸性磷酸酶(TRAP)组织化学鉴定破骨细胞。通过计数与每个细胞相关的放射自显影信号来定量生长板软骨细胞中IGF-I mRNA的丰度。在生长板增殖区和肥大区的软骨细胞中均鉴定出IGF-I mRNA。两个区域边缘的细胞所含IGF-I mRNA明显多于中央区域的细胞(p < 0.05)。此外,胫骨内侧生长板周边的IGF-I mRNA水平更高(p < 0.05),内侧的生长比外侧更活跃。IGF-I免疫反应主要存在于肥大区软骨细胞中,未观察到其分布的区域差异。在骨膜成纤维细胞中也鉴定出IGF-I mRNA和肽,特别是在肌肉附着于骨的部位,以及骨膜、骨内膜和骨髓腔内骨重塑活跃部位的成骨细胞中。在TRAP阳性破骨细胞中,检测到IGF-I免疫反应,但未检测到IGF-I mRNA。此外,在干骺端骨髓的造血细胞中均鉴定出IGF-I mRNA和肽,而在骨干中仅可检测到IGF-I免疫反应。我们得出结论,在成熟大鼠的胫骨中:(i)生长板中IGF-I基因表达与其生长和/或合成活性相关;(ii)成骨细胞和破骨细胞中存在IGF-I表明其参与了活跃的骨生长和重塑。