Odontoblast response to cavitypreparation with Er:YAG laser in ratmolars: an immunohistochemicalstudy

Odontoblast response to cavitypreparation with Er:YAG laser in ratmolars: an immunohistochemicalstudy
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成牙本质细胞对大鼠磨牙中 Er:YAG 激光制备腔体的反应:一项免疫组织化学研究

DOI:
10.1007/s10266-012-0078-x
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发表时间:
2012
期刊:
Odontology Epub 2012 Jun 27
影响因子:
--
通讯作者:
Okiji T
Okiji T
中科院分区:
--
文献类型:
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作者:
Shigetani Y;Suzuki H;Ohshima H,Yoshiba K;Yoshiba N;Okiji T

文献摘要

相似文献

本研究旨在研究用铒钇铝石榴石(Er:YAG)激光制备大鼠磨牙腔后成牙细胞系细胞的动态变化。采用Er:YAG激光在8周龄Wistar大鼠上颌左第一磨牙近中表面制备腔体。对侧第一磨牙作为未辐照对照。在激光照射后6和12小时,1、2、3、5和7天(各n= 5),立即收集标本,进行热休克蛋白(HSP)-25和巢蛋白的免疫组织化学处理,作为成牙干细胞系细胞的标记物。采用溴脱氧尿苷(BrdU)标记进行细胞增殖试验。未辐照的牙齿在成牙细胞中显示热休克蛋白-25和巢蛋白免疫反应性。照射后6 ~ 12 h,成牙细胞层组织紊乱,部分成牙细胞失去对热休克蛋白25和巢蛋白的免疫反应性。然而,在1-2天,成牙细胞层中热休克蛋白25和巢蛋白的免疫反应性显示出明显的恢复,导致成牙细胞样细胞重排,在3-7天对热休克蛋白25和巢蛋白产生强烈的免疫反应。brdu阳性细胞在第2天显著增加(与前一个时间点比较,P< 0.05;单向方差分析和scheff<s:1>事后检验),在第3天达到峰值,然后显著下降(P< 0.05)。由此可见,在本实验条件下,Er:YAG激光造腔对大鼠磨牙成牙细胞造成轻度、可逆的损伤。修复过程的特征是热休克蛋白-25和巢蛋白免疫反应性成牙细胞样细胞的重排,这发生在成牙细胞层破坏之后,这些免疫反应性部分丧失。
This study aimed to examine the dynamics of odontoblast-lineage cells following cavity preparation with erbium:yttrium–aluminum-garnet (Er:YAG) laser in rat molars. Cavity preparation was made with Er:YAG laser in the mesial surface of the maxillary left first molar of 8-week-old Wistar rats. Contralateral first molar served as unirradiated control. Immediately, 6 and 12 h and 1, 2, 3, 5 and 7 days after the lasing (n= 5, each), specimens were collected and processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin as markers for odontoblast-lineage cells. Cell proliferation assay using bromodeoxyuridine (BrdU) labeling was also performed. Unirradiated teeth showed HSP-25- and nestin-immunoreactivity in odontoblasts. At 6–12 h after irradiation, the odontoblastic layer was disorganized and some of odontoblasts lost the immunoreactivity to HSP-25 and nestin. At 1–2 days, however, HSP-25- and nestin-immunoreactivities in the odontoblast layer showed a noticeable recovery, resulting in the rearrangement of odontoblast-like cells intensely immunoreactive to HSP-25 and nestin at 3–7 days. BrdU-positive cells showed a significant increase at 2 days (P< 0.05 vs. immediate previous time point; one-way analysis of variance and Scheffé post hoc test), peaked at 3 days and then decreased significantly (P< 0.05). It was concluded that under the present experimental condition in rat molars, cavity preparation with Er:YAG laser induced mild and reversible damage to odontoblasts. The reparative process was characterized by the rearrangement of HSP-25- and nestin-immunoreactive odontoblast-like cells, which took place subsequent to the odontoblastic layer disorganization with partial loss of these immunoreactivities.