Lindahl A, Isgaard J, Isaksson O G
Endocrinology. 1987 Sep;121(3):1070-5. doi: 10.1210/endo-121-3-1070.
The effect of GH pretreatment in vivo on the colony formation of epiphyseal chondrocytes from hypophysectomized rats and the subsequent responsiveness to insulin-like growth factor (IGF-I) was studied in vitro. Chondrocytes from epiphyseal growth plates of the proximal tibia of 36-day-old hypophysectomized rats were enzymatically isolated and cultured in suspension, stabilized with agarose (0.5%) in Ham's F-12 medium and serum supplement. After 14 days the cultures were terminated and screened for cloning efficiency (number of colonies with a diameter greater than 56 microns/1000 seeded cells) and for distribution of cloning efficiency as a function of colony size. Pretreatment with human GH in vivo for 24 h (10 micrograms X 3) increased the cloning efficiency during the subsequent culture period (control, 1.5 +/- 0.1; human GH, 4.4 +/- 0.3). Addition of IGF-I to the chondrocyte cultures from control rats caused a slight increase in cloning efficiency (control, 1.5 +/- 0.1; IGF-I, 2.2 +/- 0.3) but caused a marked increase in chondrocyte cultures from GH-pretreated rats (control, 4.4 +/- 0.4; IGF-I, 8.2 +/- 0.9). The cloning efficiency was increased 12 and 24 h, but not 4 h, after start of GH-treatment in vivo. The increased responsiveness to IGF-I in vivo showed a similar time course after GH pretreatment. The distribution of cloning efficiency was altered in cultures of chondrocytes isolated from the GH-pretreated rats; large colonies were overrepresented in the GH-treated group. Colonies with a diameter exceeding 180 microns were only seen in cultures of chondrocytes isolated from the GH-pretreated animals. Addition of IGF-I in vitro did not alter the distribution of cloning efficiency, but increased the mean colony size of all colonies. Pretreatment of the rats with two different doses of IGF-I in vivo for 24 h (5 micrograms X 3 or 50 micrograms X 3) had a slight stimulatory effect on subsequent colony formation, but no potentiation of IGF-I in vitro was demonstrated. The results of the present study show that pretreatment of hypophysectomized rats with GH, but not with IGF-I, promotes the formation of chondrocyte colonies and make the chondrocytes susceptible to IGF-I in vitro. The results suggest that GH induces colony formation by IGF-I-independent mechanisms and that IGF-I is a second effector in GH action as previously shown for cultured 3T3-preadipose cells.(ABSTRACT TRUNCATED AT 400 WORDS)
研究了生长激素(GH)体内预处理对垂体切除大鼠骨骺软骨细胞集落形成以及随后对胰岛素样生长因子(IGF-I)反应性的影响。酶法分离36日龄垂体切除大鼠胫骨近端骨骺生长板的软骨细胞,将其悬浮培养,在Ham's F-12培养基和血清补充剂中用琼脂糖(0.5%)稳定。14天后终止培养,筛选克隆效率(直径大于56微米的集落数/接种的1000个细胞)以及克隆效率随集落大小的分布情况。体内用人GH预处理24小时(10微克×3次)可提高后续培养期的克隆效率(对照组,1.5±0.1;人GH组,4.4±0.3)。向对照组大鼠的软骨细胞培养物中添加IGF-I可使克隆效率略有增加(对照组,1.5±0.1;IGF-I组,2.2±0.3),但向GH预处理大鼠的软骨细胞培养物中添加IGF-I则可使其显著增加(对照组,4.4±0.4;IGF-I组,8.2±0.9)。体内开始GH处理后12小时和24小时克隆效率增加,但4小时未增加。GH预处理后对IGF-I的反应性增加显示出类似的时间进程。从GH预处理大鼠分离的软骨细胞培养物中克隆效率的分布发生了改变;GH处理组中大型集落的比例过高。直径超过180微米的集落仅在从GH预处理动物分离的软骨细胞培养物中可见。体外添加IGF-I不会改变克隆效率的分布,但会增加所有集落的平均大小。用两种不同剂量的IGF-I体内预处理大鼠24小时(5微克×3次或50微克×3次)对随后的集落形成有轻微刺激作用,但未证明体外IGF-I有增强作用。本研究结果表明,垂体切除大鼠用GH而非IGF-I预处理可促进软骨细胞集落的形成,并使软骨细胞在体外对IGF-I敏感。结果提示,GH通过不依赖IGF-I的机制诱导集落形成,并且IGF-I是GH作用中的第二个效应物,如先前对培养的3T3前脂肪细胞所显示的那样。(摘要截短至400字)