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首页> 外文期刊>Molecular and Cellular Endocrinology >Amphiregulin lacks an essential role for the bone anabolic action of parathyroid hormone
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Amphiregulin lacks an essential role for the bone anabolic action of parathyroid hormone

机译:两性调节蛋白缺乏甲状旁腺激素的骨合成代谢作用

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摘要

Although parathyroid hormone (PTH) has long been known to act as a bone anabolic agent when administered intermittently, the exact underlying mechanisms remain largely unknown. Amphiregulin (AREG), a ligand of the epidermal growth factor receptor, has been identified to be a PTH target gene in vitro and in vivo. Here, we used female global AREG knockout (AREG-KO) mice to explore the role of AREG in mediating the bone anabolic effects of PTH. AREG-KO mice were characterized by unchanged distal femoral cancellous bone mass and only subtle decreases in bone mineral density (BMD) and cortical thickness at the femoral midshaft at 3 and 8 months of age, relative to wildtype controls. AREG deficiency was associated with complex changes in the mRNA expression of other EGFR ligands in femoral cancellous bone osteoblasts in situ in 3-week-old mice. To examine the bone anabolic effects of PTH in the absence and presence of AREG, we injected 3-month-old AREG-KO females and wildtype control littermates with 80 mu g/kg PTH or vehicle 5 times per week over 4 weeks. Intermittent PTH treatment of AREG-KO mice led to increases in femoral trabecular and cortical BMD, cortical thickness, endocortical and periosteal bone formation, cancellous bone formation rate, and serum osteocalcin, comparable to those observed in wildtype control mice. In conclusion, our data indicate that the bone anabolic effects of PTH do not require AREG, at least in 3-month-old female mice. (C) 2015 The Authors. Published by Elsevier Ireland Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
机译:尽管长期以来断断续续地服用甲状旁腺激素(PTH)可以作为骨合成代谢药物,但确切的潜在机制仍然未知。表皮生长因子受体的配体双调蛋白(AREG)在体外和体内已被确定为PTH靶基因。在这里,我们使用雌性全球AREG基因敲除(AREG-KO)小鼠来研究AREG在介导PTH的骨合成代谢作用中的作用。相对于野生型对照,AREG-KO小鼠的特征是股骨远端松质骨质保持不变,并且在3和8个月大时,股骨中轴的骨矿物质密度(BMD)和皮质厚度只有微小的降低。 AREG缺乏与3周龄小鼠原位股骨松质骨成骨细胞中其他EGFR配体mRNA表达的复杂变化有关。为了检查在不存在和存在AREG的情况下PTH的骨合成代谢作用,我们在4周内每周给3个月大的AREG-KO雌性和野生型对照同窝小鼠注射80μg / kg PTH或媒介物,每周5次。与野生型对照小鼠相比,AREG-KO小鼠的间歇性PTH治疗导致股骨小梁和皮质BMD,皮质厚度,皮质内膜和骨膜骨形成,松质骨形成率以及血清骨钙素增加。总之,我们的数据表明,至少在3个月大的雌性小鼠中,PTH的骨合成代谢作用不需要AREG。 (C)2015作者。由Elsevier Ireland Ltd.发布。这是CC BY-NC-ND许可(http://creativecommons.org/licenses/by-nc-nd/4.0/)下的开放获取文章。

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