Delaisse J M, Boyde A, Maconnachie E, Ali N N, Sear C H, Eeckhout Y, Vaes G, Jones S J
International Institute of Cellular and Molecular Pathology, Universite Catholique de Louvain, Brussels, Belgium.
Bone. 1987;8(5):305-13. doi: 10.1016/8756-3282(87)90007-x.
The effects of specific inhibitors of cysteine-proteinases ((Z-Phe-Ala-CHN2: benzyloxycarbonyl-phenyl-alanyl alanyl diazomethane and E-64: trans-epoxy-succinyl-L-leucylamido(4-guanidino)-butane) and collagenase and collagenase ((Cl-1: N-(3-N-benzyloxycarbonyl amino-1-R-carboxypropyl)-L-leucyl-O-methyl-L-tyrosine N-methylamide) have been tested on the osteoclastic resorption of dentine. Chick osteoclasts were cultured in the presence or absence of 12.5 microM Z-Phe-Ala-CHN2, 40 or 60 microM E-64, or 40 or 100 microM Cl-1 for 1 or 2 days. In addition, osteoclasts were cultured on oyster shell calcitostracum with or without 12.5 microM Z-Phe-Ala-CHN2. Specimens were studied by light microscopy to count cells and resorption features and by scanning electron microscopy (SEM) stereophotogrammetry for the measurement of the depths, plan-areas and volumes of resorption pits. The numbers, depths and volumes (but not the plan-areas) of the resorption pits in dentine were significantly reduced by Z-Phe-Ala-CHN2 and E-64. Thus, for a given plan-area, the volumes and the depths of resorption pits were smaller in these experimental groups compared with control dentine specimens. The overall inhibition of resorption was at least 75%. Cl-1 did not have this inhibitory effect on the numbers or sizes of resorption pits in dentine. When the oyster calcitostracum was used as a substrate for the osteoclasts, Z-Phe-Ala-CHN2 did not reduce the numbers or volumes of pits, but increased the plan-areas and prevented the formation of deeper pits.(ABSTRACT TRUNCATED AT 250 WORDS)
已对半胱氨酸蛋白酶的特异性抑制剂((Z-苯丙氨酸-丙氨酸-CHN2:苄氧羰基-苯丙氨酰丙氨酰重氮甲烷和E-64:反式环氧琥珀酰-L-亮氨酰胺基(4-胍基)-丁烷)以及胶原酶((Cl-1:N-(3-N-苄氧羰基氨基-1-R-羧丙基)-L-亮氨酰-O-甲基-L-酪氨酸N-甲基酰胺)对牙本质破骨细胞吸收的影响进行了测试。将鸡破骨细胞在存在或不存在12.5微摩尔Z-苯丙氨酸-丙氨酸-CHN2、40或60微摩尔E-64或40或100微摩尔Cl-1的情况下培养1或2天。此外,将破骨细胞在有或没有12.5微摩尔Z-苯丙氨酸-丙氨酸-CHN2的牡蛎壳钙化层上培养。通过光学显微镜对标本进行研究以计数细胞和吸收特征,并通过扫描电子显微镜(SEM)立体摄影测量法测量吸收坑的深度、平面面积和体积。Z-苯丙氨酸-丙氨酸-CHN2和E-64可显著减少牙本质中吸收坑的数量、深度和体积(但不包括平面面积)。因此,对于给定的平面面积,与对照牙本质标本相比,这些实验组中吸收坑的体积和深度较小。吸收的总体抑制率至少为75%。Cl-1对牙本质中吸收坑的数量或大小没有这种抑制作用。当将牡蛎钙化层用作破骨细胞的底物时,Z-苯丙氨酸-丙氨酸-CHN2不会减少坑的数量或体积,但会增加平面面积并阻止形成更深的坑。(摘要截断于250字)