Department of Trauma, Plastic and Reconstructive Surgery, Goettingen University Hospital, University Medicine Goetingen, Robert Koch Str. 40, 37075 Goettingen, Germany.
J Mol Histol. 2009 Oct;40(5-6):331-41. doi: 10.1007/s10735-009-9244-z. Epub 2009 Dec 1.
Urocortin-1 (UCN) a corticotropin releasing-factor (CRF) related peptide, has been found to be expressed in many different tissues like the central nervous system, the cardiovascular system, adipose tissue, and skeletal muscle. The effects of UCN are mediated via stimulation of CRF-receptors 1 and 2 (CRFR1 and 2, CRFR's) with a high affinity for CRFR2. It has been shown that the CRF-related peptides and CRFR's are involved in the regulation of stress-related endocrine, autonomic and behavioural responses. Using immunocytochemistry, immunohistochemistry and RT-PCR, we now can show the differentiation dependent expression of UCN mRNA and peptide in human mesenchymal progenitor cells (MSCs) directed to the osteoblastic phenotype for the first time. UCN expression was down regulated by TGF-beta and BMP-2 in the early proliferation phase of osteoblast development, whereas dexamethasone (dex) minimally induced UCN gene expression during matrix maturation after 24 h stimulation. Stimulation of MSCs for 28 days with ascorbate/beta-glycerophosphate (asc/bGp) induced UCN gene expression at day 14. This effect was prevented when using 1,25-vitamin D3 or dex in addition. There was no obvious correlation to osteocalcin (OCN) gene expression in these experiments. In MSCs from patients with metabolic bone disease (n = 9) UCN gene expression was significantly higher compared to MSCs from normal controls (n = 6). Human MSCs did not express any of the CRFR's during differentiation to osteoblasts. Our results indicate that UCN is produced during the development of MSCs to osteoblasts and differentially regulated during culture as well as by differentiation factors. The expression is maximal between proliferation and matrix maturation phase. However, UCN does not seem to act on the osteoblast itself as shown by the missing CRFR's. Our results suggest new perspectives on the role of urocortin in human skeletal tissue in health and disease.
尿皮质素-1(UCN)是一种促肾上腺皮质素释放因子(CRF)相关肽,已在中枢神经系统、心血管系统、脂肪组织和骨骼肌等多种组织中发现。UCN 的作用是通过刺激 CRF 受体 1 和 2(CRFR1 和 2,CRFR)来介导的,对 CRFR2 具有高亲和力。已经表明,CRF 相关肽和 CRFR 参与了应激相关内分泌、自主和行为反应的调节。使用免疫细胞化学、免疫组织化学和 RT-PCR,我们现在可以首次显示 UCN mRNA 和肽在人间充质祖细胞(MSCs)向成骨表型分化过程中的依赖性表达。在成骨细胞发育的早期增殖阶段,TGF-β和 BMP-2 下调 UCN 表达,而地塞米松(dex)在刺激 24 小时后基质成熟期间最小程度地上调 UCN 基因表达。用抗坏血酸/β-甘油磷酸酯(asc/bGp)刺激 MSCs 28 天,在第 14 天诱导 UCN 基因表达。当在这些实验中添加 1,25-维生素 D3 或 dex 时,会阻止这种作用。在这些实验中,UCN 基因表达与骨钙素(OCN)基因表达没有明显相关性。在患有代谢性骨病的患者来源的 MSCs(n = 9)中,UCN 基因表达明显高于正常对照的 MSCs(n = 6)。在向成骨细胞分化期间,人 MSCs 不表达任何 CRFR。我们的结果表明,UCN 在 MSC 向成骨细胞的发育过程中产生,并在培养过程中以及分化因子的作用下进行差异调节。表达在增殖和基质成熟阶段达到最大值。然而,正如缺乏 CRFR 所示,UCN 似乎不会作用于成骨细胞本身。我们的结果为 UCN 在健康和疾病状态下人骨骼组织中的作用提供了新的视角。