Woods Anita, Khan Sameena, Beier Frank
Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada.
Endocrinology. 2007 Oct;148(10):5030-41. doi: 10.1210/en.2007-0695. Epub 2007 Jul 19.
C-type natriuretic peptide (CNP) has recently been identified as a key anabolic regulator of endochondral bone growth, but the cellular and molecular mechanisms involved are incompletely understood. Although CNP has been shown to stimulate proliferation and hypertrophic differentiation of growth plate chondrocytes, it is unknown whether CNP affects the earliest stages of endochondral bone development, condensation of mesenchymal precursor cells, and chondrogenesis. Here we demonstrate that CNP increases the number of chondrogenic condensations of mouse embryonic limb bud cells in micromass culture. This is accompanied by increased expression of the cell adhesion molecule N-cadherin. In addition, CNP stimulates glycosaminoglycan synthesis as indicated by increased Alcian blue staining. However, expression of the chondrogenic transcription factors Sox9, -5, and -6 or of the main extracellular matrix genes encoding collagen II and aggrecan is not affected by CNP. Instead, we show that CNP increases expression of enzymes involved in chondroitin sulfate synthesis, a required step in the production of cartilage glycosaminoglycans. In summary, we demonstrate a novel role of CNP in promoting chondrogenesis by stimulating expression of molecules involved in cell adhesion molecules and glycosaminoglycan synthesis.
C型利钠肽(CNP)最近被确定为软骨内骨生长的关键合成代谢调节因子,但其中涉及的细胞和分子机制尚不完全清楚。尽管已证明CNP可刺激生长板软骨细胞的增殖和肥大分化,但尚不清楚CNP是否影响软骨内骨发育的最早阶段,即间充质前体细胞的凝聚和成软骨过程。在此,我们证明CNP可增加微团培养中小鼠胚胎肢芽细胞的软骨形成凝聚数量。这伴随着细胞粘附分子N-钙粘蛋白表达的增加。此外,如阿尔新蓝染色增加所示,CNP可刺激糖胺聚糖合成。然而,软骨形成转录因子Sox9、-5和-6或编码胶原蛋白II和聚集蛋白聚糖的主要细胞外基质基因的表达不受CNP影响。相反,我们表明CNP可增加参与硫酸软骨素合成的酶的表达,这是软骨糖胺聚糖产生过程中的一个必要步骤。总之,我们证明了CNP通过刺激参与细胞粘附分子和糖胺聚糖合成的分子表达,在促进软骨形成中发挥了新作用。