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[人牙髓的凝集素组织化学研究。特别提及成牙本质细胞和牙髓细胞]

[Lectin histochemical study on human dental pulp. Special reference to odontoblasts and pulp cells].

作者信息

Endo K

出版信息

Meikai Daigaku Shigaku Zasshi. 1989;18(3):360-81.

PMID:2489677
Abstract

The present study investigated some lectin affinities of human dental pulps, especially of odontoblasts and pulp cells. The materials were obtained from clinically intact teeth that were caries-free, attrition and/or abrasion-free. Mucopolysaccharide staining was carried out with applied PAS and alcian blue (AB) (pH 1.0 and 2.5). Lectins used were Con A, WGA, RCA-1, UEA-1, DBA, SBA, MPA, LFA, HPA, PNA, and GS-1, and the avidin-biotin peroxidase complex method was employed. Some specimens were tested for PNA binding after treatment with sialidase. The following results were obtained: 1) On PAS and AB staining, the pulp tissue was very weakly or borderline positive. 2) Lectin binding in odontoblasts was intensely positive with Con A, WGA, RCA-1, MPA, and LFA, but negative or very weakly positive with the other lectins examined. 3) Lectin localization in odontoblasts was localized diffusely throughout the cytoplasm. 4) On PNA staining, odontoblasts were negative, but changed to positive after treatment with sialidase. 5) Odontoblast processes showed negative or borderline staining with all lectins used in this study. 6) The pulp cells were clearly positive with Con A, MPA, LFA, RCA-1, and SBA and especially LFA showed an intense reaction with the pulp cells. 7) WGA affinity for odontoblasts was very strong but that for pulp cells was very weak. 8) Lectin binding in pulp cells was observed mainly in the processes of the cells. From the above results, it is clear that the lectin binding pattern of odontoblasts differs from that of pulp cells. The data suggest that D-mannose, N-acetyl-D-glucosamine, D-galactose, and N-acetyl-D-galactosamine residues are localized in the odontoblasts and sialic acid is localized in the pulp cells.

摘要

本研究调查了人牙髓组织,尤其是成牙本质细胞和牙髓细胞的一些凝集素亲和力。材料取自临床检查完整、无龋、无磨损的牙齿。采用过碘酸雪夫氏反应(PAS)和阿尔辛蓝(AB)(pH 1.0和2.5)进行黏多糖染色。所用凝集素包括刀豆球蛋白A(Con A)、小麦胚芽凝集素(WGA)、蓖麻凝集素-1(RCA-1)、荆豆凝集素-1(UEA-1)、大豆凝集素(DBA)、大豆凝集素(SBA)、麦胚凝集素(MPA)、扁豆凝集素(LFA)、辣根过氧化物酶标记的凝集素(HPA)、花生凝集素(PNA)和麦芽凝集素(GS-1),并采用抗生物素蛋白-生物素过氧化物酶复合物法。部分标本经唾液酸酶处理后检测PNA结合情况。结果如下:1)PAS和AB染色显示,牙髓组织呈弱阳性或临界阳性。2)成牙本质细胞中,Con A、WGA、RCA-1、MPA和LFA的凝集素结合呈强阳性,而其他检测的凝集素呈阴性或弱阳性。3)成牙本质细胞中的凝集素定位弥漫分布于整个细胞质。4)PNA染色时,成牙本质细胞呈阴性,但经唾液酸酶处理后变为阳性。5)本研究中使用的所有凝集素对成牙本质细胞突均呈阴性或临界染色。6)牙髓细胞对Con A、MPA、LFA、RCA-1和SBA呈明显阳性,尤其是LFA与牙髓细胞反应强烈。7)WGA对成牙本质细胞的亲和力很强,但对牙髓细胞的亲和力很弱。8)牙髓细胞中的凝集素结合主要见于细胞突起。根据上述结果,显然成牙本质细胞的凝集素结合模式与牙髓细胞不同。数据表明,D-甘露糖、N-乙酰-D-葡萄糖胺、D-半乳糖和N-乙酰-D-半乳糖胺残基定位于成牙本质细胞,而唾液酸定位于牙髓细胞。

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