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成人永久性甲状腺软骨中的血管内皮生长因子表达:对软骨不发生骨化的影响

VEGF expression in adult permanent thyroid cartilage: implications for lack of cartilage ossification.

作者信息

Pufe Thomas, Mentlein Rolf, Tsokos Michael, Steven Philipp, Varoga Deike, Goldring Mary B, Tillmann Bernhard N, Paulsen Friedrich P

机构信息

Institute of Anatomy, Christian-Albrechts-University, Kiel, Germany.

出版信息

Bone. 2004 Aug;35(2):543-52. doi: 10.1016/j.bone.2004.02.026.

Abstract

Vascular endothelial growth factor (VEGF) has been shown to play an important role during endochondral bone formation in hypertrophic cartilage remodeling, ossification, and angiogenesis, but it is not expressed in normal adult articular cartilage. Thyroid cartilage undergoes only partial ossification beginning at the age of about 20. Because it never completely ossifies, we investigated a possible role of VEGF and its receptors (VEGFRs) as well as the angiogenetic inhibitor endostatin in this permanent cartilage. In analysis of cartilage samples from all specimens evaluated, VEGF121 and VEGF165 were identified as the only VEGF splice forms expressed. In addition to VEGF, VEGFR-2 (kinase domain region/fetal liver kinase 1), but not VEGFR-1 (fms-like tyrosine kinase 1), was detectable by RT-PCR in cartilage. However, VEGFR-2 expression was only detectable up to the age of 19 years. Deposition of VEGF and VEGFR was confirmed by immunohistochemistry. VEGF concentrations measured by ELISA in thyroid cartilage increased with age in males but decreased in females. Endostatin concentrations measured by ELISA in thyroid cartilage were three times lower than in articular cartilage and showed no change with age, either in females or males. VEGF was immunostained within the intra- and pericellular matrices of some but not all chondrocytes. Thus, apart from its production in hypertrophic chondrocytes of growth plates, VEGF is also produced in single chondrocytes of thyroid cartilage. The data allow us to speculate that thyroid cartilage persists in an embryological state until it has reached its final size. After reaching its final size at the end of the second decade, VEGFR-2 is downregulated and ossification starts in the posterior part of the thyroid cartilage, proceeding ventrally. Both proteins, VEGF121 and VEGF165, should contribute to this process. VEGF concentration is high and changes in an age-related and sex-specific manner. Therefore, we postulate that VEGF is at least one of the key factors that is important for the lifelong ossification in thyroid cartilage.

摘要

血管内皮生长因子(VEGF)已被证明在软骨内骨形成过程中,在肥大软骨重塑、骨化和血管生成方面发挥重要作用,但在正常成人关节软骨中不表达。甲状腺软骨从大约20岁开始仅发生部分骨化。由于它从未完全骨化,我们研究了VEGF及其受体(VEGFRs)以及血管生成抑制剂内皮抑素在这种永久性软骨中的可能作用。在对所有评估标本的软骨样本进行分析时,VEGF121和VEGF165被确定为仅表达的VEGF剪接形式。除VEGF外,通过RT-PCR在软骨中可检测到VEGFR-2(激酶结构域区域/胎儿肝激酶1),但未检测到VEGFR-1(fms样酪氨酸激酶1)。然而,VEGFR-2表达仅在19岁之前可检测到。通过免疫组织化学证实了VEGF和VEGFR的沉积。通过ELISA测量的甲状腺软骨中的VEGF浓度在男性中随年龄增加而升高,但在女性中降低。通过ELISA测量的甲状腺软骨中的内皮抑素浓度比关节软骨低三倍,并且在女性或男性中均未显示随年龄变化。VEGF在一些但不是所有软骨细胞的细胞内和细胞周围基质中进行免疫染色。因此,除了在生长板的肥大软骨细胞中产生外,VEGF也在甲状腺软骨的单个软骨细胞中产生。这些数据使我们推测,甲状腺软骨在达到其最终大小之前一直处于胚胎状态。在第二个十年末达到其最终大小后,VEGFR-2被下调,甲状腺软骨后部开始骨化,并向腹侧进行。VEGF121和VEGF165这两种蛋白质都应该有助于这一过程。VEGF浓度很高,并且以与年龄和性别相关的方式变化。因此,我们假设VEGF至少是对甲状腺软骨终身骨化很重要的关键因素之一。

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