Takagi M, Parmley R T, Denys F R
J Histochem Cytochem. 1983 Sep;31(9):1089-100. doi: 10.1177/31.9.6136541.
Proteoglycans (PGs) are closely associated with cartilage calcification. We have examined the hypertrophic zone of rat epiphyseal cartilage, in which calcification is occurring, using the high-iron diamine-thiocarbohydrazide-silver proteinate (HID-TCH-SP) method for sulfated glycosaminoglycans, an immunoferritin method specific for chondroitin sulfate A, and the tannic acid-ferric chloride (TA-Fe) method to stain cartilage matrix granules (MGs) presumed to be PG monomers. HID-TCH-SP produced stain deposits with a diameter of 11.2 +/- 3.2 nm (mean +/- SD; n = 200) in the MGs. However, HID-TCH-SP staining was not discernible in membrane-limited matrix vesicles (MVs). In areas of advanced calcification, partially disrupted MVs and globular bodies (GBs), derived in part from disrupted and/or degenerated MVs, contained a few too many small HID-TCH-SP stain deposits. Further down the epiphyseal cartilage, intact MVs markedly decreased and the GBs, containing many small HID-TCH-SP stain deposits, significantly increased in number. These GBs were found exclusively in the longitudinal septa rather than in the transverse septa. After enzyme digestion with testicular hyaluronidase, small (7.2 +/- 1.2 nm in diameter) stain deposits remained in the MGs and GBs, presumably localized to keratan sulfate. Immunoferritin localizing chondroitin sulfate strongly stained MGs, whereas MVs and GBs lacked staining. TA-Fe staining of glycoconjugates in the GBs demonstrated a striking decrease in the diameter of MGs associated with calcification in the GBs as compared with those in the noncalcifying area around the GBs. These results indicate that the GBs containing needle-like apatite crystals in morphologic preparations represent sites of chondroitin sulfate degradation. Testicular hyaluronidase-resistant sulfated glycosaminoglycans presumed to be keratan sulfate and partially degraded PGs selectively remain within the GBs as a probable requisite for expansion of the initial calcification in MVs.
蛋白聚糖(PGs)与软骨钙化密切相关。我们使用高铁二胺 - 硫代碳酰肼 - 银蛋白法(HID - TCH - SP)检测硫酸化糖胺聚糖、软骨素硫酸酯A特异性免疫铁蛋白法以及单宁酸 - 氯化铁(TA - Fe)法对大鼠骨骺软骨的肥大区进行了研究,该肥大区正在发生钙化,TA - Fe法用于染色推测为PG单体的软骨基质颗粒(MGs)。HID - TCH - SP在MGs中产生直径为11.2±3.2 nm(平均值±标准差;n = 200)的染色沉积物。然而,在膜包被的基质小泡(MVs)中未观察到HID - TCH - SP染色。在钙化进展区域,部分破裂的MVs和球状小体(GBs)(部分源自破裂和/或退化的MVs)含有少量过多的小HID - TCH - SP染色沉积物。在骨骺软骨更靠下的部位,完整的MVs明显减少,而含有许多小HID - TCH - SP染色沉积物的GBs数量显著增加。这些GBs仅在纵向隔中发现,而非横向隔中。用睾丸透明质酸酶进行酶消化后,小的(直径7.2±1.2 nm)染色沉积物保留在MGs和GBs中,推测定位于硫酸角质素。定位软骨素硫酸酯的免疫铁蛋白强烈染色MGs,而MVs和GBs缺乏染色。GBs中糖缀合物的TA - Fe染色显示,与GBs周围非钙化区域的MGs相比,与GBs钙化相关的MGs直径显著减小。这些结果表明,形态学制剂中含有针状磷灰石晶体的GBs代表软骨素硫酸酯降解部位。推测为硫酸角质素且部分降解的PGs中对睾丸透明质酸酶有抗性的硫酸化糖胺聚糖作为MVs中初始钙化扩展的可能必要条件选择性地保留在GBs内。