Jing Y, Zhou X, Han X, Jing J, von der Mark K, Wang J, de Crombrugghe B, Hinton R J, Feng J Q
Department of Biomedical Sciences, Texas A&M Baylor College of Dentistry, Dallas, TX, USA.
Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Dent Res. 2015 Dec;94(12):1668-75. doi: 10.1177/0022034515598135. Epub 2015 Sep 4.
For decades, it has been widely accepted that hypertrophic chondrocytes undergo apoptosis prior to endochondral bone formation. However, very recent studies in long bone suggest that chondrocytes can directly transform into bone cells. Our initial in vivo characterization of condylar hypertrophic chondrocytes revealed modest numbers of apoptotic cells but high levels of antiapoptotic Bcl-2 expression, some dividing cells, and clear alkaline phosphatase activity (early bone marker). Ex vivo culture of newborn condylar cartilage on a chick chorioallantoic membrane showed that after 5 d the cells on the periphery of the explants had begun to express Col1 (bone marker). The cartilage-specific cell lineage-tracing approach in triple mice containing Rosa 26(tdTomato) (tracing marker), 2.3 Col1(GFP) (bone cell marker), and aggrecan Cre(ERT2) (onetime tamoxifen induced) or Col10-Cre (activated from E14.5 throughout adult stage) demonstrated the direct transformation of chondrocytes into bone cells in vivo. This transformation was initiated at the inferior portion of the condylar cartilage, in contrast to the initial ossification site in long bone, which is in the center. Quantitative data from the Col10-Cre compound mice showed that hypertrophic chondrocytes contributed to ~80% of bone cells in subchondral bone, ~70% in a somewhat more inferior region, and ~40% in the most inferior part of the condylar neck (n = 4, P < 0.01 for differences among regions). This multipronged approach clearly demonstrates that a majority of chondrocytes in the fibrocartilaginous condylar cartilage, similar to hyaline cartilage in long bones, directly transform into bone cells during endochondral bone formation. Moreover, ossification is initiated from the inferior portion of mandibular condylar cartilage with expansion in one direction.
几十年来,人们普遍认为肥大软骨细胞在软骨内骨形成之前会发生凋亡。然而,最近对长骨的研究表明,软骨细胞可以直接转化为骨细胞。我们最初对髁突肥大软骨细胞的体内特征分析显示,凋亡细胞数量适中,但抗凋亡蛋白Bcl-2表达水平较高,有一些分裂细胞,并且碱性磷酸酶活性明显(早期骨标志物)。新生髁突软骨在鸡绒毛尿囊膜上的体外培养表明,5天后外植体周边的细胞开始表达Col1(骨标志物)。在含有Rosa 26(tdTomato)(追踪标志物)、2.3 Col1(GFP)(骨细胞标志物)和聚集蛋白聚糖Cre(ERT2)(单次他莫昔芬诱导)或Col10-Cre(从E14.5到成年期全程激活)的三联小鼠中采用软骨特异性细胞谱系追踪方法,证明了软骨细胞在体内可直接转化为骨细胞。这种转化起始于髁突软骨的下部,与长骨的初始骨化部位在中央不同。来自Col10-Cre复合小鼠的定量数据显示,肥大软骨细胞在软骨下骨中贡献了约80%的骨细胞,在稍低区域贡献了约70%,在髁突颈部最下部贡献了约40%(n = 4,各区域间差异P < 0.01)。这种多方面的研究方法清楚地表明,纤维软骨性髁突软骨中的大多数软骨细胞,与长骨中的透明软骨类似,在软骨内骨形成过程中直接转化为骨细胞。此外,骨化从下颌髁突软骨的下部开始,并向一个方向扩展。