Lozito Thomas P, Tuan Rocky S
Center for Cellular and Molecular Engineering, Department of Orthopaedic Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Center for Cellular and Molecular Engineering, Department of Orthopaedic Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Dev Biol. 2015 Mar 15;399(2):249-62. doi: 10.1016/j.ydbio.2014.12.036. Epub 2015 Jan 14.
Lizards capable of caudal autotomy exhibit the remarkable ability to "drop" and then regenerate their tails. However, the regenerated lizard tail (RLT) is known as an "imperfect replicate" due to several key anatomical differences compared to the original tail. Most striking of these "imperfections" concerns the skeleton; instead of the vertebrae of the original tail, the skeleton of the RLT takes the form of an unsegmented cartilage tube (CT). Here we have performed the first detailed staging of skeletal development of the RLT CT, identifying two distinct mineralization events. CTs isolated from RLTs of various ages were analyzed by micro-computed tomography to characterize mineralization, and to correlate skeletal development with expression of endochondral ossification markers evaluated by histology and immunohistochemistry. During early tail regeneration, shortly after CT formation, the extreme proximal CT in direct contact with the most terminal vertebra of the original tail develops a growth plate-like region that undergoes endochondral ossification. Proximal CT chondrocytes enlarge, express hypertrophic markers, including Indian hedgehog (Ihh), apoptose, and are replaced by bone. During later stages of tail regeneration, the distal CT mineralizes without endochondral ossification. The sub-perichondrium of the distal CT expresses Ihh, and the perichondrium directly calcifies without cartilage growth plate formation. The calcified CT perichondrium also contains a population of stem/progenitor cells that forms new cartilage in response to TGF-β stimulation. Treatment with the Ihh inhibitor cyclopamine inhibited both proximal CT ossification and distal CT calcification. Thus, while the two mineralization events are spatially, temporally, and mechanistically very different, they both involve Ihh. Taken together, these results suggest that Ihh regulates CT mineralization during two distinct stages of lizard tail regeneration.
能够进行尾自切的蜥蜴展现出了非凡的能力,即“脱落”然后再生其尾巴。然而,由于与原始尾巴相比存在一些关键的解剖学差异,再生蜥蜴尾巴(RLT)被称为“不完美的复制品”。这些“不完美”中最显著的是骨骼方面;RLT的骨骼不是原始尾巴的椎骨,而是呈无节段软骨管(CT)的形式。在此,我们首次对RLT CT的骨骼发育进行了详细分期,确定了两个不同的矿化事件。通过微计算机断层扫描分析从不同年龄的RLT分离出的CT,以表征矿化,并将骨骼发育与通过组织学和免疫组织化学评估的软骨内骨化标记物的表达相关联。在早期尾巴再生过程中,CT形成后不久,与原始尾巴最末端椎骨直接接触的最近端CT会发育出一个类似生长板的区域,该区域会经历软骨内骨化。近端CT软骨细胞增大,表达包括印度刺猬因子(Ihh)在内的肥大标记物,凋亡,然后被骨替代。在尾巴再生的后期阶段,远端CT在没有软骨内骨化的情况下矿化。远端CT的软骨膜下层表达Ihh,并且软骨膜直接钙化,没有形成软骨生长板。钙化的CT软骨膜还包含一群干/祖细胞,它们在受到转化生长因子-β刺激时会形成新的软骨。用Ihh抑制剂环杷明处理可抑制近端CT骨化和远端CT钙化。因此,虽然这两个矿化事件在空间、时间和机制上有很大不同,但它们都涉及Ihh。综上所述,这些结果表明Ihh在蜥蜴尾巴再生的两个不同阶段调节CT矿化。