Elisabeth Ytteborg, Jacob Torgersen, Grete Baeverfjord, Harald Takle
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To characterize the fusion process we analyzed an intermediate and a terminal stage of the pathology by using x-ray, histology, immunohistochemistry, real-time quantitative PCR and in situ hybridization. At early stage in the fusion process, disorganized and proliferating osteoblasts were prominent at the growth zones of the vertebral body endplates. PCNA positive cells further extended along the rims of fusing vertebral bodies. During the developing pathology, the marked border between the osteoblast growth zones and the chondrocytic areas connected to the arches became less distinct, as proliferating cells and chondrocytes blended through an intermediate zone. This cell proliferation appeared to be closely linked to fusion of opposing arch centra. During the fusion process a metaplastic shift appeared in the arch centra where cells in the intermediate zone between osteoblasts and chondrocytes co-expressed mixed signals of chondrogenic and osteogenic markers. A similar shift also occurred in the notochord where proliferating chordoblasts changed transcription profile from chondrogenic to also include osteogenic marker genes. In progressed fusions, arch centra and intervertebral space mineralized.</p><p><strong>Conclusion: </strong>Loss of cell integrity through cell proliferation and metaplastic shifts seem to be key events in the fusion process. The fusion process involves molecular regulation and cellular changes similar to those found in mammalian deformities, indicating that salmon is suitable for studying general bone development and to be a comparative model for spinal deformities.</p>","PeriodicalId":35905,"journal":{"name":"BMC Physiology","volume":"10 ","pages":"13"},"PeriodicalIF":0.0000,"publicationDate":"2010-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909226/pdf/","citationCount":"0","resultStr":"{\"title\":\"Morphological and molecular characterization of developing vertebral fusions using a teleost model.\",\"authors\":\"Elisabeth Ytteborg, Jacob Torgersen, Grete Baeverfjord, Harald Takle\",\"doi\":\"10.1186/1472-6793-10-13\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Spinal disorders are a major cause of disability for humans and an important health problem for intensively farmed animals. 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During the developing pathology, the marked border between the osteoblast growth zones and the chondrocytic areas connected to the arches became less distinct, as proliferating cells and chondrocytes blended through an intermediate zone. This cell proliferation appeared to be closely linked to fusion of opposing arch centra. During the fusion process a metaplastic shift appeared in the arch centra where cells in the intermediate zone between osteoblasts and chondrocytes co-expressed mixed signals of chondrogenic and osteogenic markers. A similar shift also occurred in the notochord where proliferating chordoblasts changed transcription profile from chondrogenic to also include osteogenic marker genes. In progressed fusions, arch centra and intervertebral space mineralized.</p><p><strong>Conclusion: </strong>Loss of cell integrity through cell proliferation and metaplastic shifts seem to be key events in the fusion process. 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引用次数: 0
摘要
背景:脊柱疾病是导致人类残疾的一个主要原因,也是集约化养殖动物的一个重要健康问题。实验表明,脊椎畸形的病因复杂,但在不同物种之间具有可比性。然而,人们对导致骨骼畸形的分子机制还知之甚少。为了进一步解释其中的机制,我们研究了大西洋鲑鱼(Salmo salar)骨代谢和脊椎融合发病机制的基本方面:在实验中,将幼年鲑鱼置于高热条件下,28%以上的鲑鱼椎体发生融合。为了描述融合过程的特征,我们使用 X 射线、组织学、免疫组化、实时定量 PCR 和原位杂交分析了病理的中期和末期阶段。在融合过程的早期阶段,椎体内板生长区的成骨细胞杂乱无章且不断增殖。PCNA 阳性细胞沿着融合椎体的边缘进一步延伸。在病理发展过程中,成骨细胞生长区和与椎弓相连的软骨细胞区之间的明显边界变得不那么明显,因为增殖细胞和软骨细胞通过中间区域混合在一起。这种细胞增殖似乎与对立的足弓中心融合密切相关。在融合过程中,拱形中心出现了移行转变,处于成骨细胞和软骨细胞中间区域的细胞共同表达软骨和成骨标记的混合信号。类似的转变也发生在脊索,增殖的脊索母细胞改变了转录谱,从软骨生成基因转录到成骨标记基因。在进展的融合过程中,椎弓中心和椎间隙矿化:结论:通过细胞增殖和移行转变丧失细胞完整性似乎是融合过程中的关键事件。融合过程涉及的分子调控和细胞变化与哺乳动物畸形中发现的类似,表明鲑鱼适合研究一般骨骼发育,并可作为脊柱畸形的比较模型。
Morphological and molecular characterization of developing vertebral fusions using a teleost model.
Background: Spinal disorders are a major cause of disability for humans and an important health problem for intensively farmed animals. Experiments have shown that vertebral deformities present a complex but comparable etiology across species. However, the underlying molecular mechanisms involved in bone deformities are still far from understood. To further explicate the mechanisms involved, we have examined the fundamental aspects of bone metabolism and pathogenesis of vertebral fusions in Atlantic salmon (Salmo salar).
Results: Experimentally, juvenile salmon were subjected to hyperthermic conditions where more than 28% developed fused vertebral bodies. To characterize the fusion process we analyzed an intermediate and a terminal stage of the pathology by using x-ray, histology, immunohistochemistry, real-time quantitative PCR and in situ hybridization. At early stage in the fusion process, disorganized and proliferating osteoblasts were prominent at the growth zones of the vertebral body endplates. PCNA positive cells further extended along the rims of fusing vertebral bodies. During the developing pathology, the marked border between the osteoblast growth zones and the chondrocytic areas connected to the arches became less distinct, as proliferating cells and chondrocytes blended through an intermediate zone. This cell proliferation appeared to be closely linked to fusion of opposing arch centra. During the fusion process a metaplastic shift appeared in the arch centra where cells in the intermediate zone between osteoblasts and chondrocytes co-expressed mixed signals of chondrogenic and osteogenic markers. A similar shift also occurred in the notochord where proliferating chordoblasts changed transcription profile from chondrogenic to also include osteogenic marker genes. In progressed fusions, arch centra and intervertebral space mineralized.
Conclusion: Loss of cell integrity through cell proliferation and metaplastic shifts seem to be key events in the fusion process. The fusion process involves molecular regulation and cellular changes similar to those found in mammalian deformities, indicating that salmon is suitable for studying general bone development and to be a comparative model for spinal deformities.
BMC PhysiologyBiochemistry, Genetics and Molecular Biology-Physiology
CiteScore
9.60
自引率
0.00%
发文量
0
期刊介绍:
BMC Physiology is an open access journal publishing original peer-reviewed research articles in cellular, tissue-level, organismal, functional, and developmental aspects of physiological processes. BMC Physiology (ISSN 1472-6793) is indexed/tracked/covered by PubMed, MEDLINE, BIOSIS, CAS, EMBASE, Scopus, Zoological Record and Google Scholar.