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大鼠牙胚中骨钙素(Gla蛋白)的免疫定位:间接免疫荧光法、过氧化物酶-抗过氧化物酶法、抗生物素蛋白-生物素-过氧化物酶复合物法以及抗生物素蛋白-生物素-金复合物银增强法之间的比较

Immunolocalization of Gla proteins (osteocalcin) in rat tooth germs: comparison between indirect immunofluorescence, peroxidase-antiperoxidase, avidin-biotin-peroxidase complex, and avidin-biotin-gold complex with silver enhancement.

作者信息

Bronckers A L, Gay S, Finkelman R D, Butler W T

出版信息

J Histochem Cytochem. 1987 Aug;35(8):825-30. doi: 10.1177/35.8.3298423.

Abstract

Odontoblasts and osteoblasts synthesize gamma-carboxyglutamatic acid (Gla)-containing proteins which are partially deposited in the mineralizing tissues and partially released into the plasma. Using four immunostaining techniques, we have evaluated the question of whether dentin Gla proteins (DGP) are transported to the mineralization front through the odontoblast processes. Undecalcified sections of rat incisors and molar tooth germs were immunostained with affinity-purified antibodies to DGP using the following methods: indirect immunofluorescence; peroxidase-antiperoxidase (PAP); avidin-biotin-peroxidase complex (ABC-peroxidase); and avidin-biotin-gold complex with silver enhancement (ABC-GSS). The results obtained with these four procedures were compared with respect to the developmental appearance of DGP, staining intensity and presence in odontoblastic processes, predentin, dentin, and blood vessels. Qualitatively, similar results were obtained with the four, with respect to the distribution and developmental appearance of DGP, with two exceptions: indirect immunofluorescence never stained DGP within blood vessels, whereas the other methods occasionally did; and because of its sensitivity, only the ABC-GSS method revealed immunostaining for DGP in odontoblastic processes. All methods revealed weak immunostaining in predentin which was considerably enhanced with hyaluronidase treatment; however, hyaluronidase only moderately increased predentin immunostaining with ABC-GSS. Of these four procedures, ABC-GSS is the most sensitive; however, ABC-GSS appears to detect predominantly antigens at the surface of tissue sections. We conclude that DGP is present in odontoblastic processes but in low amounts; the weak staining was due either to rapid transport of DGP through the process or to the fact that this mode of transport is limited.

摘要

成牙本质细胞和成骨细胞合成含γ-羧基谷氨酸(Gla)的蛋白质,这些蛋白质部分沉积在矿化组织中,部分释放到血浆中。我们使用四种免疫染色技术,评估了牙本质Gla蛋白(DGP)是否通过成牙本质细胞突起转运至矿化前沿这一问题。采用以下方法,用针对DGP的亲和纯化抗体对大鼠切牙和磨牙牙胚的未脱钙切片进行免疫染色:间接免疫荧光法;过氧化物酶-抗过氧化物酶法(PAP);抗生物素蛋白-生物素-过氧化物酶复合物法(ABC-过氧化物酶法);以及抗生物素蛋白-生物素-金复合物银增强法(ABC-GSS)。就DGP的发育表现、染色强度以及在成牙本质细胞突起、前期牙本质、牙本质和血管中的存在情况,对这四种方法得到的结果进行了比较。定性而言,就DGP的分布和发育表现,这四种方法得到了相似的结果,但有两个例外:间接免疫荧光法从未在血管内染出DGP,而其他方法偶尔能染出;并且由于其敏感性,只有ABC-GSS法在成牙本质细胞突起中显示出DGP的免疫染色。所有方法在前期牙本质中均显示出弱阳性染色,经透明质酸酶处理后染色显著增强;然而,透明质酸酶仅适度增加了ABC-GSS法对前期牙本质的免疫染色。在这四种方法中,ABC-GSS法最敏感;然而,ABC-GSS法似乎主要检测组织切片表面的抗原。我们得出结论,DGP存在于成牙本质细胞突起中,但含量较低;弱阳性染色要么是由于DGP通过突起的快速转运,要么是由于这种转运方式有限。

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