Jegat Nadège, Septier Dominique, Veis Arthur, Poliard Anne, Goldberg Michel
Oral Biology, EA 2496, Faculté de Chirurgie Dentaire, Université Paris Descartes, Montrouge, France.
Head Face Med. 2007 Dec 21;3:40. doi: 10.1186/1746-160X-3-40.
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.
为了研究两种生物活性低分子釉原蛋白A+4和A-4的短期效应,在上颌第一磨牙近中面制备半月形洞,牙髓暴露后,将单独的琼脂糖珠(对照组)或浸泡在A+4或A-4中的珠子(实验组)植入牙髓。1、3或7天后,处死大鼠,通过免疫组织化学研究牙齿。通过PCNA标记研究细胞增殖,A+4在第3天呈阳性,但在第7天下降,而A-4在3至7天之间持续保持高水平。与A+4相比,A-4通过RP59标记显示的向骨/成牙本质细胞谱系的分化更明显。A-4在第3天和第7天骨桥蛋白阳性细胞相似。相比之下,对于A+4,第3天检测到的弱标记在第7天变强。牙本质涎蛋白(DSP)是一种体内成牙本质细胞标志物,直到第7天才可检测到,在A-4刺激后有一些细胞变为DSP阳性,但A+4刺激后则没有。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,A-4(第3天)的作用比A+4(第7天)更早熟。目前的数据表明A+/-4促进了成骨祖细胞的早期募集,并证明了A+4和A-4之间的功能差异。