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人胎儿牙齿中基底膜IV型胶原和IV型胶原酶(基质金属蛋白酶-2和基质金属蛋白酶-9)的表达

Expression of basement membrane type IV collagen and type IV collagenases (MMP-2 and MMP-9) in human fetal teeth.

作者信息

Heikinheimo K, Salo T

机构信息

Institute of Dentistry, University of Turku, Finland.

出版信息

J Dent Res. 1995 May;74(5):1226-34. doi: 10.1177/00220345950740051301.

DOI:10.1177/00220345950740051301
PMID:7790601
Abstract

Formation and degradation of dental basement membrane (BM) are important for tooth development. Data on the expression of genes for type IV collagen (the major structural component of the BM) and type IV collagenases [MMP-2 (72 kDa) and MMP-9 (92 kDa)], enzymes that degrade type IV collagen during human tooth development, are lacking. We studied expression of type IV collagen and the MMP-2 and MMP-9 in human fetal teeth (from the 13th to the 20th gestational weeks, covering cap stage through early hard tissue formation). During cap and bell stages, in situ hybridization located transcripts for alpha 1 type IV collagen chain in the fibroblasts surrounding the enamel organ. No alpha 1 type IV collagen chain mRNA was detected in tooth germ epithelium or dental papilla. However, type IV collagen immunoreactivity was observed in BM underlying the dental epithelium up to the appositional stage. Transcripts for MMP-2 were located mostly in the cells of the dental papilla and follicle. Transient expression of MMP-2 mRNA was observed in the inner enamel epithelium of late cap/early bell-stage teeth. During early apposition, a high level of MMP-2 was confined to secretory odontoblasts. Transcripts for MMP-9 were detected by the sensitive reverse-transcription polymerase chain reaction (RT-PCR) in developing teeth. Thus, in dental BM, alpha 1 type IV collagen chain may be of mesenchymal cell origin. Further, MMP-2 but not MMP-9 may participate in remodeling and degradation of BM during human tooth morphogenesis.

摘要

牙基底膜(BM)的形成和降解对牙齿发育至关重要。关于IV型胶原蛋白(BM的主要结构成分)基因以及IV型胶原酶[基质金属蛋白酶-2(72 kDa)和基质金属蛋白酶-9(92 kDa)](在人类牙齿发育过程中降解IV型胶原蛋白的酶)表达的数据尚缺乏。我们研究了人类胎儿牙齿(妊娠第13至20周,涵盖帽状期至早期硬组织形成)中IV型胶原蛋白以及基质金属蛋白酶-2和基质金属蛋白酶-9的表达。在帽状期和钟状期,原位杂交在釉器周围的成纤维细胞中定位到了α1 IV型胶原链的转录本。在牙胚上皮或牙乳头中未检测到α1 IV型胶原链mRNA。然而,在牙上皮下方的BM中直至牙本质形成期均观察到IV型胶原蛋白免疫反应性。基质金属蛋白酶-2的转录本主要定位在牙乳头和滤泡的细胞中。在帽状期末期/钟状期早期牙齿的内釉上皮中观察到基质金属蛋白酶-2 mRNA的短暂表达。在早期牙本质形成期,高水平的基质金属蛋白酶-2局限于分泌性成牙本质细胞。通过灵敏的逆转录聚合酶链反应(RT-PCR)在发育中的牙齿中检测到了基质金属蛋白酶-9的转录本。因此,在牙BM中,α1 IV型胶原链可能起源于间充质细胞。此外,在人类牙齿形态发生过程中,可能是基质金属蛋白酶-2而非基质金属蛋白酶-9参与了BM的重塑和降解。

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