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Short-term effects of amelogenin gene splice products A+4 and A-4 implanted in the exposed rat molar pulp

机译:牙釉蛋白基因剪接产物A + 4和A-4植入暴露于大鼠磨牙牙髓的短期效应

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摘要

In order to study the short-time effects of two bioactive low-molecular amelogenins A+4 and A-4, half-moon cavities were prepared in the mesial aspect of the first maxillary molars, and after pulp exposure, agarose beads alone (controls) or beads soaked in A+4 or A-4 (experimental) were implanted into the pulp. After 1, 3 or 7 days, the rats were killed and the teeth studied by immunohistochemistry. Cell proliferation was studied by PCNA labeling, positive at 3 days, but decreasing at day 7 for A+4, whilst constantly high between 3 and 7 days for A-4. The differentiation toward the osteo/odontoblast lineage shown by RP59 labeling was more apparent for A-4 compared with A+4. Osteopontin-positive cells were alike at days 3 and 7 for A-4. In contrast, for A+4, the weak labeling detected at day 3 became stronger at day 7. Dentin sialoprotein (DSP), an in vivo odontoblast marker, was not detectable until day 7 where a few cells became DSP positive after A-4 stimulation, but not for A+4. These results suggest that A +/- 4 promote the proliferation of some pulp cells. Some of them further differentiate into osteoblast-like progenitors, the effects being more precocious for A-4 (day 3) compared with A+4 (day 7). The present data suggest that A +/- 4 promote early recruitment of osteogenic progenitors, and evidence functional differences between A+4 and A-4.
机译:为了研究两种具有生物活性的低分子促黄素生成素A + 4和A-4的短期作用,在第一个上颌磨牙的近旁部分制备了半月型腔,在牙髓暴露后,单独使用琼脂糖珠(对照)或将浸泡在A + 4或A-4(实验)中的珠子植入纸浆。在1、3或7天后,将大鼠处死并通过免疫组织化学研究牙齿。通过PCNA标记研究了细胞增殖,在3天时阳性,但对于A + 4在第7天下降,而对于A-4则在3至7天持续高。与A + 4相比,RP-4标记显示的对骨/成牙本质细胞系的分化更为明显。对于A-4,骨桥蛋白阳性细胞在第3天和第7天相似。相比之下,对于A + 4,在第3天检测到的弱标记在第7天变得更强。直到第7天,在A-4后一些细胞的DSP呈阳性后,才能检测到体内成牙本质成牙本质标志物牙本质唾液蛋白(DSP)。刺激,但不适用于A + 4。这些结果表明,A +/- 4促进了一些牙髓细胞的增殖。其中一些进一步分化为成骨细胞样祖细胞,与A + 4(第7天)相比,A-4(第3天)的效果更早。目前的数据表明A +/- 4促进成骨祖细胞的早期募集,并证明A + 4和A-4之间的功能差异。

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