Shapiro I M, Golub E E, Chance B, Piddington C, Oshima O, Tuncay O C, Frasca P, Haselgrove J C
Department of Biochemistry, University of Pennsylvania, Philadelphia 19104-6003.
Dev Biol. 1988 Oct;129(2):372-9. doi: 10.1016/0012-1606(88)90384-3.
The objective of this investigation was to investigate the relationship between the energy status of epiphyseal chondrocytes of the chick growth cartilage and the development of mineralization. A microfluorimetric scanning technique was used to measure the reduced pyridine nucleotide content of transverse sections of freeze-trapped cartilage; these measurements were related to tissue structure by scanning electron microscopy. The results of this study show that the energy status of cells in the hypertrophic region of the growth cartilage is more complex than was previously believed. In hypertrophic cartilage, most chondrocytes are in a reduced state. However, in the early hypertrophic region, the vascular channels that penetrate the cartilage from the metaphysis exert a profound local effect on the energy metabolism of perivascular chondrocytes. Thus, around each of the channels, there exists a zone of chondrocytes about 40-60 micron wide which exhibits a low fluorescence yield. The fluorescence level suggests that these perivascular cells have a higher level of oxidative metabolism than hypertrophic chondrocytes that are a distance (greater than 150 micron) from the vascular channels. This finding, in conjunction with our earlier observation that mineralization is first seen in the perivascular region, leads us to the conclusion that mineralization is associated with cellular oxidative activity. We now reject the long-held concept that in cartilage the development of mineralization is entirely due to tissue hypoxia.
本研究的目的是探讨雏鸡生长软骨骨骺软骨细胞的能量状态与矿化发育之间的关系。采用微荧光扫描技术测量冷冻捕获软骨横切面中还原型吡啶核苷酸的含量;通过扫描电子显微镜将这些测量结果与组织结构相关联。本研究结果表明,生长软骨肥大区域细胞的能量状态比以前认为的更为复杂。在肥大软骨中,大多数软骨细胞处于还原状态。然而,在早期肥大区域,从干骺端穿透软骨的血管通道对血管周围软骨细胞的能量代谢产生深远的局部影响。因此,在每个通道周围,存在一个宽约40-60微米的软骨细胞区,其荧光产率较低。荧光水平表明,这些血管周围细胞的氧化代谢水平高于距血管通道一定距离(大于150微米)的肥大软骨细胞。这一发现,结合我们早期观察到矿化首先出现在血管周围区域,使我们得出结论,矿化与细胞氧化活性有关。我们现在摒弃了长期以来的观念,即软骨中的矿化发育完全是由于组织缺氧。