Yoshida E, Noshiro M, Kawamoto T, Tsutsumi S, Kuruta Y, Kato Y
Department of Biochemistry, Hiroshima University Faculty of Dentistry, Hiroshima, 734-8553, Japan.
Exp Cell Res. 2001 Apr 15;265(1):64-72. doi: 10.1006/excr.2001.5161.
Indian hedgehog (Ihh) is highly expressed in prehypertrophic chondrocytes in vivo and has been proposed to regulate the proliferation and maturation of chondrocytes and bone collar formation in the growth plate. In high-density cultures of rabbit growth-plate chondrocytes, Ihh mRNA was also expressed at the highest level in the prehypertrophic stage. To explore endogenous factors that regulate Ihh expression in chondrocytes, we examined the effects of various growth factors on Ihh mRNA expression in this system. Retinoic acid (RA) and bone morphogenetic protein-2 enhanced Ihh mRNA expression, whereas PTH/PTH-related peptide (PTHrP) markedly suppressed Ihh expression. RA at more than 10(-8) M induced the expression of Ihh and Patched 1 (Ptc1) within 3 h, before it increased the type X collagen mRNA level at 6-24 h. Cycloheximide blocked the up-regulation of Ihh by RA, indicating the requirement of de novo protein synthesis for this stimulation. These findings suggest that RA is involved in the up-regulation of Ihh during endochondral bone formation. In contrast to RA, PTH (1-84) at 10(-7) M abolished the mRNA expression of Ihh and Ptc1 within 2-4 h, before it suppressed the expression of type X collagen at 12-24 h. The inhibition of Ihh expression by PTH (1-84) did not require de novo protein synthesis. PTH (1-34), PTHrP (1-34), and (Bu)(2)cAMP also suppressed Ihh expression. On the other hand, Ihh has been reported to induce PTHrP synthesis in the perichondrium. Consequently, the direct inhibitory action of PTH/PTHrP on Ihh appears to be a negative feedback mechanism that prevents excess PTHrP accumulation in cartilage.
印度刺猬因子(Ihh)在体内的前肥大软骨细胞中高度表达,有人提出它可调节软骨细胞的增殖和成熟以及生长板中骨环的形成。在兔生长板软骨细胞的高密度培养中,Ihh mRNA在肥大前期也表达至最高水平。为了探究调节软骨细胞中Ihh表达的内源性因素,我们在此系统中检测了各种生长因子对Ihh mRNA表达的影响。视黄酸(RA)和骨形态发生蛋白-2增强了Ihh mRNA的表达,而甲状旁腺激素/甲状旁腺激素相关肽(PTHrP)则显著抑制Ihh的表达。浓度超过10^(-8) M的RA在3小时内诱导Ihh和patched 1(Ptc1)的表达,之后在6 - 24小时增加X型胶原mRNA水平。放线菌酮阻断了RA对Ihh的上调作用,表明这种刺激需要从头合成蛋白质。这些发现提示RA参与了软骨内骨形成过程中Ihh的上调。与RA相反,10^(-7) M的甲状旁腺激素(1 - 84)在2 - 4小时内消除了Ihh和Ptc1的mRNA表达,之后在12 - 24小时抑制X型胶原的表达。甲状旁腺激素(1 - 84)对Ihh表达的抑制不需要从头合成蛋白质。甲状旁腺激素(1 - 34)、甲状旁腺激素相关肽(1 - 34)和双丁酰环磷腺苷(Bu)2cAMP也抑制Ihh的表达。另一方面,据报道Ihh可诱导软骨膜中甲状旁腺激素相关肽的合成。因此,甲状旁腺激素/甲状旁腺激素相关肽对Ihh的直接抑制作用似乎是一种负反馈机制,可防止甲状旁腺激素相关肽在软骨中过度积累。