Koyama Eiki, Ochiai Takanaga, Rountree Ryan B, Kingsley David M, Enomoto-Iwamoto Motomi, Iwamoto Masahiro, Pacifici Maurizio
Department of Orthopaedic Surgery, Thomas Jefferson University, College of Medicine, Philadelphia, PA 19107, USA.
Ann N Y Acad Sci. 2007 Nov;1116:100-12. doi: 10.1196/annals.1402.063.
Indian hedgehog (Ihh) has been previously found to regulate synovial joint formation. To analyze mechanisms, we carried out morphological, molecular, and cell fate map analyses of interzone and joint development in wild-type and Ihh(-/-) mouse embryo long bones. We found that Ihh(-/-) cartilaginous digit anlagen remained fused and lacked interzones or mature joints, whereas wrist skeletal elements were not fused but their joints were morphologically abnormal. E14.5 and E17.5 wild-type digit and ankle prospective joints expressed hedgehog target genes including Gli1 and Gli2 and interzone-associated genes including Gdf5, Erg, and tenascin-C, but expression of all these genes was barely detectable in mutant joints. For cell fate map analysis of joint progenitor cells, we mated Gdf5-Cre(+/-)/Rosa R26R(+/-) double transgenic mice with heterozygous Ihh(+/-) mice and monitored reporter beta-galactosidase activity and gene expression in triple-transgenic progeny. In control Gdf5-Cre(+/-)/R26R(+/-)/Ihh(+/-) limbs, reporter-positive cells were present in developing interzones, articulating layers, and synovial lining tissue and absent from underlying growth plates. In mutant Gdf5-Cre(+/-)/R26R(+/-)/Ihh(-/-) specimens, reporter-positive cells were present also. However, the cells were mostly located around the prospective and uninterrupted digit joint sites and, interestingly, still expressed Erg, tenascin-C, and Gdf5. Topographical analysis revealed that interzone and associated cells were not uniformly distributed, but were much more numerous ventrally. A similar topographical bias was seen for cavitation process and capsule primordia formation. In sum, Ihh is a critical and possibly direct regulator of joint development. In its absence, distribution and function of Gdf5-expressing interzone-associated cells are abnormal, but their patterning at prospective joint sites still occurs. The joint-forming functions of the cells appear to normally involve a previously unsuspected asymmetric distribution along the ventral-to-dorsal plane of the developing joint.
先前已发现印度刺猬信号蛋白(Ihh)可调节滑膜关节的形成。为分析其机制,我们对野生型和Ihh基因敲除(Ihh(-/-))小鼠胚胎长骨的中间带及关节发育进行了形态学、分子学和细胞命运图谱分析。我们发现,Ihh(-/-)小鼠的软骨指原基仍融合在一起,缺乏中间带或成熟关节,而腕部骨骼元件未融合,但关节形态异常。胚胎期第14.5天(E14.5)和第17.5天(E17.5)的野生型指关节和踝关节的预期关节表达刺猬信号通路靶基因,包括Gli1和Gli2,以及与中间带相关的基因,包括Gdf5、Erg和腱生蛋白-C,但在突变关节中几乎检测不到所有这些基因的表达。为了对关节祖细胞进行细胞命运图谱分析,我们将Gdf5-Cre(+/-)/Rosa R26R(+/-)双转基因小鼠与杂合Ihh(+/-)小鼠交配,并监测三转基因后代中的报告基因β-半乳糖苷酶活性和基因表达。在对照Gdf5-Cre(+/-)/R26R(+/-)/Ihh(+/-)肢体中,报告基因阳性细胞存在于发育中的中间带、关节层和滑膜衬里组织中,而在下方的生长板中不存在。在突变的Gdf5-Cre(+/-)/R26R(+/-)/Ihh(-/-)标本中,也存在报告基因阳性细胞。然而,这些细胞大多位于预期的和未中断的指关节部位周围,有趣的是,它们仍然表达Erg、腱生蛋白-C和Gdf5。地形分析显示,中间带及相关细胞分布并不均匀,腹侧数量更多。在空化过程和关节囊原基形成过程中也观察到类似的地形偏向。总之,Ihh是关节发育的关键且可能是直接调节因子。在其缺失的情况下,表达Gdf5的中间带相关细胞的分布和功能异常,但它们在前瞻性关节部位的模式化仍会发生。这些细胞的关节形成功能似乎通常涉及沿发育中关节腹背平面的一种先前未被怀疑的不对称分布。