Department of Orthopaedics, Dongguk University Ilsan Hospital, Goyang 410-773, Republic of Korea.
Biochem Biophys Res Commun. 2012 May 18;421(4):819-24. doi: 10.1016/j.bbrc.2012.04.096. Epub 2012 Apr 25.
While several isoforms of parathyroid hormone-related peptide (PTHrP) have been commercially available, the difference in their effect has not been widely studied. The purpose of this study was to determine which isoform most effectively promoted chondrogenesis and suppressed hypertrophy from mesenchymal stem cells (MSCs). MSCs isolated from fresh bone marrow were cultured in pellet in chondrogenic medium containing 5 ng/ml of transforming growth factor (TGF)-β(3). From day 14 of culture, subsets of pellets were additionally treated with one of the four PTHrP isoforms (1-34, 1-86, 7-34, and 107-139) at 100 nM. After a further 2 weeks of in vitro culture, pellets were harvested for analysis. PTHrPs 1-34 and 1-86 significantly decreased the DNA level (p<0.05) while PTHrPs 7-34 and 107-139 significantly increased DNA level (p<0.05) compared with the control treated with TGF-β(3) only. Glycosaminoglycan per DNA significantly increased when treated with PTHrPs 1-34 and 1-86 (p<0.05) while it significantly decreased with PTHrPs 7-34 and 107-139 (p<0.05). PTHrP 1-34 significantly increased the gene and protein expression of the chondrogenic marker COL2A1, and decreased those of hypertrophic markers COL10A1 and alkaline phosphatase while other isoforms showed inconsistent effects. All of PTHrP isoforms significantly suppressed the gene and protein expression of indian hedgehog (p<0.05) while all isoforms except PTHrP 107-139 significantly reduced the gene and protein expression of patched 1 (p<0.05). In conclusion, of several PTHrP isoforms, PTHrP 1-34 most significantly enhanced chondrogenesis and suppressed hypertrophy in MSCs, supporting its use for cartilage tissue engineering.
虽然已经有几种甲状旁腺激素相关肽(PTHrP)的同工型可商业化获得,但它们的作用差异尚未得到广泛研究。本研究旨在确定哪种同工型最有效地促进软骨形成并抑制间充质干细胞(MSCs)的肥大。从新鲜骨髓中分离出的 MSCs 在含有 5ng/ml 转化生长因子(TGF)-β(3)的软骨形成培养基中进行微球培养。从培养的第 14 天开始,部分微球球另外用四种 PTHrP 同工型(1-34、1-86、7-34 和 107-139)之一在 100nM 浓度下处理。在体外培养进一步 2 周后,收获微球进行分析。与仅用 TGF-β(3)处理的对照组相比,PTHrPs 1-34 和 1-86 显著降低了 DNA 水平(p<0.05),而 PTHrPs 7-34 和 107-139 则显著增加了 DNA 水平(p<0.05)。用 PTHrPs 1-34 和 1-86 处理时,糖胺聚糖与 DNA 的比值显著增加(p<0.05),而用 PTHrPs 7-34 和 107-139 处理时则显著降低(p<0.05)。PTHrP 1-34 显著增加了软骨形成标志物 COL2A1 的基因和蛋白表达,并降低了肥大标志物 COL10A1 和碱性磷酸酶的表达,而其他同工型则表现出不一致的作用。所有 PTHrP 同工型均显著抑制了印度刺猬(Indian hedgehog,IHH)的基因和蛋白表达(p<0.05),而除了 PTHrP 107-139 之外的所有同工型均显著降低了 patched 1 的基因和蛋白表达(p<0.05)。总之,在几种 PTHrP 同工型中,PTHrP 1-34 最显著地增强了 MSCs 的软骨形成并抑制了肥大,支持其用于软骨组织工程。