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甲状腺激素调节生长板中硫酸乙酰肝素蛋白聚糖的表达。

Thyroid hormone regulates heparan sulfate proteoglycan expression in the growth plate.

作者信息

Bassett J H D, Swinhoe R, Chassande O, Samarut J, Williams G R

机构信息

Molecular Endocrinology Group, Division of Medicine and Medical Research Council Clinical Sciences Centre, Hammersmith Hospital, Du Cane Road, London W12 0NN, United Kingdom.

出版信息

Endocrinology. 2006 Jan;147(1):295-305. doi: 10.1210/en.2005-0485. Epub 2005 Oct 13.

Abstract

Thyroid hormone is essential for normal skeletal development. Hypothyroidism is associated with growth arrest, failure of chondrocyte differentiation, and abnormal matrix synthesis. Thyroid hormone modulates the Indian hedgehog/PTHrP feedback loop and regulates fibroblast growth factor (FGF)/FGF receptor signaling. Because heparan sulfate (HS) proteoglycans (Prgs) (HSPGs) are absolutely required by these signaling pathways, we have investigated whether thyroid status affects HSPG expression within the growth plate. Tibial growth plate sections were obtained from 12-wk-old rats rendered euthyroid, thyrotoxic, or hypothyroid at 6 wk of age, 14-d-old congenitally hypothyroid Pax8-null mice, and TRalpha/TRbeta double-null mice lacking all thyroid hormone receptors. HS and chondroitin sulfate Prg expression was determined by immunohistochemistry using three monoclonal antibodies. There was increased HS staining in growth plates from hypothyroid animals predominantly within the extracellular matrix of reserve and proliferative zones. Cellular HS staining was also increased particularly in prehypertrophic chondrocytes. T3 regulation of HSPG core protein and HS synthetic and modification enzyme expression was studied in ATDC5 cells using semiquantitative RT-PCR. Thyroid hormone negatively regulated expression of the core protein Gpc6, the polymerase Ext1, and the modification enzyme Hs6st2. These studies demonstrate that the expression and distribution of growth plate Prgs are regulated by thyroid hormone, and the regulation of HSPG expression provides an important additional link between FGF and Indian hedgehog signaling and T3. These novel observations suggest that the cartilage matrix and especially HSPGs are critical mediators of the skeletal response to thyroid hormone.

摘要

甲状腺激素对正常骨骼发育至关重要。甲状腺功能减退与生长停滞、软骨细胞分化失败及基质合成异常有关。甲状腺激素调节印度刺猬因子/甲状旁腺激素相关蛋白反馈回路,并调节成纤维细胞生长因子(FGF)/FGF受体信号传导。由于这些信号通路绝对需要硫酸乙酰肝素(HS)蛋白聚糖(Prgs)(HSPGs),我们研究了甲状腺状态是否会影响生长板内HSPG的表达。从6周龄时甲状腺功能正常、甲状腺功能亢进或甲状腺功能减退的12周龄大鼠、14日龄先天性甲状腺功能减退的Pax8基因敲除小鼠以及缺乏所有甲状腺激素受体的TRα/TRβ双基因敲除小鼠获取胫骨生长板切片。使用三种单克隆抗体通过免疫组织化学法测定HS和硫酸软骨素Prg的表达。甲状腺功能减退动物的生长板中HS染色增加,主要在储备区和增殖区的细胞外基质内。细胞HS染色也增加,特别是在肥大前软骨细胞中。使用半定量逆转录聚合酶链反应在ATDC5细胞中研究了甲状腺激素对HSPG核心蛋白以及HS合成和修饰酶表达的调节。甲状腺激素对核心蛋白Gpc6、聚合酶Ext1和修饰酶Hs6st2的表达起负调节作用。这些研究表明生长板Prgs的表达和分布受甲状腺激素调节,HSPG表达的调节在FGF和印度刺猬因子信号传导与T3之间提供了一个重要的额外联系。这些新发现表明软骨基质尤其是HSPGs是骨骼对甲状腺激素反应的关键介质。

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