Stringa E, Tuan R S
Department of Orthopedic Surgery, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Anat Embryol (Berl). 1996 Nov;194(5):427-37. doi: 10.1007/BF00185990.
The embryonic skull bone, the calvarium, develops via intramembranous ossification, whereby mesenchymal cells differentiate directly into osteoblasts. However, under certain conditions, such as systemic calcium deficiency, regions of cartilage-like tissue are observed in the chick embryonic calvarium, suggesting the presence of pre-cartilage cells. We have recently identified and isolated a chondrogenic cell subpopulation from chick embryonic calvarium by Percoll gradient centrifugation. Using peanut agglutinin (PNA), which has been shown to bind specifically to chondroprogenitor cells in various developing skeletal elements, we have further examined the chondrogenic characteristics of calvarial cells. Histochemical staining of calvaria sections showed the presence of PNA-binding cells in subcambial regions of the calvarium as a function of embryonic development and calcium status. PNA-binding activity was also used as the basis for affinity chromatography fractionation of calvarial cells isolated from normal and calcium-deficient, shell-less chick embryos. A higher percentage of calvarial cells from the normal embryo bound PNA than those from shell-less embryos. Interestingly, more PNA-binding cells were found in the dense, chondrogenic fractions obtained by prior Percoll gradient fractionation of calvarial cells. The chondrogenic potential of the PNA affinity fractionated cells was assessed in culture based on alcian blue staining, and expression of collagen type II and aggrecan core protein. PNA-binding cells isolated from total calvarial cells and from the dense Percoll fractions exhibited a prominent chondrocyte-like phenotype, and were organized in alcian blue-stained nodules, which immunostained positively for collagen type II and aggrecan. Expression of collagen type II was also detected at the mRNA level by means of coupled reverse transcription/polymerase chain reaction. On the other hand, non-PNA-binding cells, isolated from total calvarial cells and from the lighter Percoll fractions, were primarily fibroblastic in appearance and did not express cartilage-associated characteristics. The presence of distinct PNA-binding cells with chondrogenic potential strongly suggests that these cells may be functionally important in morphogenesis of the embryonic calvarium.
胚胎颅骨,即颅盖,通过膜内成骨发育,在此过程中,间充质细胞直接分化为成骨细胞。然而,在某些条件下,如全身性钙缺乏时,在鸡胚胎颅盖中可观察到软骨样组织区域,这表明存在软骨前体细胞。我们最近通过Percoll梯度离心从鸡胚胎颅盖中鉴定并分离出了一个软骨生成细胞亚群。利用已证明能特异性结合各种发育中的骨骼元素中的软骨祖细胞的花生凝集素(PNA),我们进一步研究了颅盖细胞的软骨生成特性。颅盖切片的组织化学染色显示,颅盖的亚生发层区域存在PNA结合细胞,其数量随胚胎发育和钙状态而变化。PNA结合活性还被用作从正常和缺钙的无壳鸡胚胎中分离的颅盖细胞亲和层析分离的基础。正常胚胎的颅盖细胞中结合PNA的细胞百分比高于无壳胚胎。有趣的是,在通过先前对颅盖细胞进行Percoll梯度分级分离得到的致密软骨生成级分中发现了更多的PNA结合细胞。基于阿尔新蓝染色以及Ⅱ型胶原蛋白和聚集蛋白聚糖核心蛋白的表达,在培养中评估了PNA亲和分级分离细胞的软骨生成潜力。从总颅盖细胞和致密Percoll级分中分离出的PNA结合细胞表现出显著的软骨细胞样表型,并组织成阿尔新蓝染色的结节,这些结节对Ⅱ型胶原蛋白和聚集蛋白聚糖免疫染色呈阳性。还通过逆转录/聚合酶链反应偶联在mRNA水平检测到了Ⅱ型胶原蛋白的表达。另一方面,从总颅盖细胞和较轻的Percoll级分中分离出的非PNA结合细胞,外观主要为成纤维细胞样,不表达与软骨相关的特征。具有软骨生成潜力的独特PNA结合细胞的存在强烈表明,这些细胞可能在胚胎颅盖的形态发生中具有重要功能。