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甲状旁腺激素在体外可增强人皮肤来源前体细胞向成骨细胞的分化。

Parathyroid hormone enhances osteoblast differentiation from human skin derived precursor cells in vitro.

作者信息

Suriyachand Katesaree, Bunyaratvej Ahnond, Bunyaratavej Narong, Sila-Asna Monnipha

机构信息

Department of Pathology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 2011 Oct;94 Suppl 5:S1-6.

Abstract

Parathyroid hormone (PTH), a new effective treatment for osteoporosis patients which promotes the anabolic effect in vivo, can enhance the differentiation of osteoblasts derived from the human skin-derived precursor cells (hSKPs) in vitro culture. This research investigated the effects of PTH by studying the gene expressions and other markers of osteoblast differentiation along with the induction of hSKPs to osteoblast in two experiment groups, i.e. the osteogenic induction medium (OM) only and the OM plus PTH (OM + PTH). The results of each type were compared between these two groups. Both groups expressed the Cbfa1 gene, a regulator of osteoblasts and also one of the most osteoblast specific genes. The findings were that the OM + PTH group showed more intense alkaline phosphatase staining than the other. The gene expressions of protein showing the mature osteoblasts like osteocalcin (OCN) and bone sialoprotein (BSP) in the OM + PTH group expressed higher and faster (Day 14) than the OM group. Moreover, the gene expression of osteoprotegerin (OPG) possessing the protein produced by the mature osteoblasts showed a higher level in the OM + PTH group on the same day as OCN and BSP occurred. This protein performs a function in inhibiting osteoclast maturation. The present study found that PTH enhanced the differentiation of osteoblasts derived from hSKPs by promoting the maturation of osteoblasts in vitro. It possibly concerns with the anabolic effect of PTH in a treatment for osteoporosis patients. Additionally, hSKPs are the interesting sources for osteoporosis treatments when combining with PTH.

摘要

甲状旁腺激素(PTH)是一种对骨质疏松症患者有效的新疗法,可在体内促进合成代谢作用,在体外培养中能增强源自人皮肤来源前体细胞(hSKPs)的成骨细胞分化。本研究通过在两个实验组中研究成骨细胞分化的基因表达和其他标志物以及将hSKPs诱导为成骨细胞,来探究PTH的作用,这两个实验组分别是仅使用成骨诱导培养基(OM)和使用OM加PTH(OM + PTH)。比较了两组中每种类型的结果。两组均表达Cbfa1基因,它是成骨细胞的一种调节因子,也是最具成骨细胞特异性的基因之一。结果发现,OM + PTH组的碱性磷酸酶染色比另一组更强。在OM + PTH组中,显示成熟成骨细胞的蛋白质如骨钙素(OCN)和骨唾液蛋白(BSP)的基因表达比OM组更高且更快(第14天)。此外,在与OCN和BSP出现的同一天,具有成熟成骨细胞产生的蛋白质的骨保护素(OPG)的基因表达在OM + PTH组中更高。这种蛋白质具有抑制破骨细胞成熟的功能。本研究发现,PTH通过促进体外成骨细胞的成熟来增强源自hSKPs的成骨细胞的分化。这可能与PTH在治疗骨质疏松症患者中的合成代谢作用有关。此外,当与PTH联合使用时,hSKPs是治疗骨质疏松症的有趣来源。

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