Axelsson I, Pita J C, Howell D S, Lorentzon R, Berman I, Boquist L
University of Miami School of Medicine, Florida.
Pediatr Res. 1990 Jan;27(1):41-4. doi: 10.1203/00006450-199001000-00014.
The metabolism of proteoglycans in normal growth plate and the changes in growth plate morphology induced by diabetes and malnutrition were studied in rats. The proteoglycans had a significantly faster turnover (half-life measured with [35S]sulfate labeling: 25-30 h) than the cells in the growth plate. Morphometric studies showed significant reductions of cell number, zone height, and [3H]thymidine incorporation in growth plates from rats with untreated streptozotocin-induced diabetes compared to normal rats. Similar, although less pronounced alterations were observed in malnourished, nondiabetic rats. Disaggregation and degradation of proteoglycans are probably necessary prerequisites for calcification. Our data indicate that the proteoglycans are in a dynamic state of rapid biosynthesis and degradation throughout the growth plate with a shift in the balance at the calcification front toward less synthesis and more degradation.
研究了大鼠正常生长板中蛋白聚糖的代谢以及糖尿病和营养不良诱导的生长板形态变化。蛋白聚糖的周转速度(用[35S]硫酸盐标记测量的半衰期:25 - 30小时)明显快于生长板中的细胞。形态计量学研究表明,与正常大鼠相比,未经治疗的链脲佐菌素诱导糖尿病大鼠的生长板中细胞数量、区域高度和[3H]胸苷掺入量显著减少。在营养不良的非糖尿病大鼠中观察到类似但不太明显的变化。蛋白聚糖的分解和解聚可能是钙化的必要先决条件。我们的数据表明,蛋白聚糖在整个生长板中处于快速生物合成和降解的动态状态,在钙化前沿平衡向合成减少和降解增加的方向转变。