首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Differential regulation of GDF-5 and FGF-2/4 by immobilisation in ovo exposes distinct roles in joint formation.
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Differential regulation of GDF-5 and FGF-2/4 by immobilisation in ovo exposes distinct roles in joint formation.

机译:通过固定在卵中对GDF-5和FGF-2 / 4的差异调节,揭示了关节形成中的不同作用。

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摘要

Members of the fibroblast growth factor (FGF) family and growth and differentiation factor 5 (GDF-5) have been implicated in joint specification, but their roles in subsequent cavity formation are not defined. Cavity formation (cavitation) depends upon limb movement in embryonic chicks and factors involved in joint formation are often identified by their expression at the joint-line. We have sought support for the roles of FGF-2, FGF-4, and GDF-5 in cavitation by defining expression patterns, immunohistochemically, during joint formation and establishing whether these are modified by in ovo immobilisation. We found that FGF-2 exhibited low level nuclear expression in chondrocytes and fibrocartilage cells close to presumptive joints, but showed significantly higher expression levels in cells at, and directly bordering, the forming joint cavity. This high-level joint line FGF-2 expression was selectively diminished in immobilised limbs. In contrast, we show that FGF-4 does not exhibit differential joint-line expression and was unaffected by immobilisation. GDF-5 protein also failed to show joint-line selective labelling, and although immobilisation induced a cartilaginous fusion across presumptive joints, it did not affect cellular GDF-5 expression patterns. Examining changes in GDF-5 expression in response to a direct mechanical strain stimulus in primary embryonic chick articular surface (AS) cells in vitro discloses only small mechanically-induced reductions in GDF-5 expression, suggesting that GDF-5 does not exert a direct positive contribution to the mechano-dependent joint cavitation process. This notion was supported by retroviral overexpression of UDPGD, a characteristic factor involved in hyaluronan (HA) accumulation at presumptive joint lines, which was also found to produce small decreases in AS cell GDF-5 expression. These findings support a direct mechano-dependent role for FGF-2, but not FGF-4, in the cavitation process and indicate that GDF-5 is likely to influence chondrogenesis positively without contributing directly to joint cavity formation.
机译:成纤维细胞生长因子(FGF)家族成员和生长与分化因子5(GDF-5)的成员已牵涉到联合规范中,但尚未定义它们在随后的腔形成中的作用。空洞的形成(空化)取决于雏鸡的肢体运动,并且通常通过它们在关节线上的表达来确定参与关节形成的因素。我们通过在关节形成过程中通过免疫组织化学定义表达模式并确定卵内固定是否修饰这些表达模式,来寻求对FGF-2,FGF-4和GDF-5在空化中的作用的支持。我们发现FGF-2在靠近假定关节的软骨细胞和纤维软骨细胞中表现出低水平的核表达,但是在形成关节腔处并与之直接接壤的细胞中表现出明显更高的表达水平。在固定的肢体中,这种高水平的关节细胞FGF-2表达选择性降低。相反,我们表明FGF-4不会显示差异的联合表达,并且不受固定化的影响。 GDF-5蛋白也未能显示关节选择性标记,尽管固定化诱导了假定关节之间的软骨融合,但它并不影响细胞GDF-5的表达方式。体外检查原代鸡雏关节表面(AS)细胞中直接机械应变刺激引起的GDF-5表达变化,发现仅机械诱导的GDF-5表达小幅降低,表明GDF-5不会直接发挥作用对依赖机械力的空化过程的积极贡献。 UDPGD的逆转录病毒过表达支持了这一观点,UDPGD是在假定的关节细胞中参与透明质酸(HA)积累的特征因子,还发现它会导致AS细胞GDF-5表达的少量降低。这些发现支持空化过程中FGF-2(而不是FGF-4)具有直接的机械依赖性作用,并表明GDF-5可能在不直接促进关节腔形成的情况下积极地影响软骨形成。

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