Ishizeki K, Takigawa M, Nawa T, Suzuki F
Department of Oral Anatomy, Iwate Medical University School of Dentistry, Morioka, Japan.
Anat Rec. 1996 May;245(1):25-35. doi: 10.1002/(SICI)1097-0185(199605)245:1<25::AID-AR5>3.0.CO;2-E.
We reported that when Meckel's cartilage was transplanted ectopically, chondrocytes transformed into osteocyte-like cells accompanying the extracellular calcified matrix. However, we could not determine whether the osteocyte-like cells were derived from host tissues or from Meckel's cartilage itself. Therefore, we examined whether the Meckel's cartilage chondrocytes, which have a retrogressive ultimate fate, are capable of inducing the observed calcification and further transform into osteocyte-like cells in culture.
Meckelian chondrocytes isolated enzymatically were plated at a low density and grown in alpha-MEM containing 10% FBS at 37 degrees C under 5% CO2 in air for up to 4 weeks.
Chondrocytes were fibroblast-like cells early in culture, but gradually transformed from polygonal cells into typical chondrocytes showing metachromasia with toluidine blue staining. After an additional week of culture, the chondrocytes transformed from large to small round cells accompanying nodule formations. Small round cells multiple-layered actively, and showed more intense alkaline phosphatase (ALPase) activity. Immunostaining identified type II collagen in the extracellular matrix at 2 weeks of culture, and type I collagen and osteocalcin were later synthesized by round cells. von Kossa's reaction showed extensive precipitation of calcification throughout the flocculent materials. Ultrastructural analysis showed that the cells surrounded by calcified matrix strongly resembled osteocytes.
The present study suggested that the Meckel's cartilage chondrocytes can express the osteocyte-like phenotype in vitro during synthesis of bone-type marker proteins such as osteocalcin or type I collagen.
我们曾报道,当梅克尔软骨异位移植时,软骨细胞会伴随细胞外钙化基质转化为骨细胞样细胞。然而,我们无法确定这些骨细胞样细胞是源自宿主组织还是梅克尔软骨本身。因此,我们研究了具有退行性最终命运的梅克尔软骨软骨细胞是否能够在培养中诱导观察到的钙化,并进一步转化为骨细胞样细胞。
通过酶法分离的梅克尔软骨细胞以低密度接种,在含10%胎牛血清的α - MEM培养基中,于37℃、5%二氧化碳的空气中培养长达4周。
培养早期软骨细胞呈成纤维细胞样,但逐渐从多边形细胞转变为经甲苯胺蓝染色显示异染性的典型软骨细胞。再培养一周后,软骨细胞从大的圆形细胞转变为小的圆形细胞并形成结节。小圆形细胞积极多层排列,并显示出更强的碱性磷酸酶(ALPase)活性。免疫染色在培养2周时在细胞外基质中鉴定出II型胶原蛋白,随后圆形细胞合成I型胶原蛋白和骨钙素。冯·科萨反应显示在整个絮状物质中广泛存在钙化沉淀。超微结构分析表明,被钙化基质包围的细胞与骨细胞非常相似。
本研究表明,梅克尔软骨软骨细胞在合成骨型标记蛋白如骨钙素或I型胶原蛋白的过程中,能够在体外表达骨细胞样表型。