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Divergent activities of osteogenic BMP2 and tenogenic BMP12 and BMP13 independent of receptor binding affinities

机译:成骨性BMP2张力性BMP12和BMP13的发散活性独立于受体结合亲和力

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摘要

Ectopic expression of recombinant human bone morphogenetic protein 2 (rhBMP2) induces osteogenesis, while ectopic expression of rhBMP12 and rhBMP13 induces the formation of tendon-like tissue. Despite their different in vivo activities, all three ligands bound to the type I bone morphogenic protein receptors (BMPRs), activin receptor-like kinase (ALK)-3 and ALK6, and to the type II BMPRs, activin receptor type-2A, activin receptor type-2B, and BMPR2, with similar affinities. Treatment of C3H10T1/2 cells with rhBMP2 activated SMAD signaling and induced expression of osteoblast markers including osteocalcin mRNA (Ocn). In contrast, treatment with rhBMP12 or rhBMP13 resulted in a dose-dependent induction of a tendon-specific gene (Thbs4) expression with no detectable activation of SMAD 1, 5, and 8. Differential regulation of Thbs4 and Ocn has potential utility as an in vitro biomarker for induction of tenogenic signaling. Such an assay also permits the ability to distinguish between the activities of different BMPs and may prove useful in studies on the molecular mechanisms of BMP tenogenic activity.
机译:重组人骨形态发生蛋白2(rhBMP2)的异位表达诱导成骨,而rhBMP12和rhBMP13的异位表达诱导肌腱样组织的形成。尽管它们的体内活性不同,但所有三个配体均与I型骨形态发生蛋白受体(BMPR),激活素受体样激酶(ALK)-3和ALK6结合,并与II型BMPR,激活素受体2A型,激活素结合具有相似亲和力的2B型受体和BMPR2。用rhBMP2处理C3H10T1 / 2细胞可激活SMAD信号传导并诱导成骨细胞标志物(包括骨钙素mRNA(Ocn))的表达。相反,用rhBMP12或rhBMP13处理导致剂量依赖性地诱导肌腱特异性基因(Thbs4)表达,而SMAD 1、5和8均未检测到激活。Thbs4和Ocn的差异调节具有潜在的效用。体外生物标记物,用于诱导肌腱信号传导。这种测定法还允许区分不同BMP活性的能力,并可能被证明可用于研究BMP肌腱活性的分子机制。

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