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Apoptosis of odontoclasts under physiological root resorption of human deciduous teeth.

机译:人乳牙的生理性根吸收下的成牙本质细胞的凋亡。

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This study was designed to establish the apoptosis of odontoclasts during physiological root resorption of human deciduous teeth. Deciduous teeth were fixed, decalcified, and embedded in paraffin for immunohistochemical (IHC) observations and in Epon for transmission electron microscopy (TEM). Apoptotic cells were identified by terminal deoxynucleotidyl transferase (TdT)-mediated dUTP-digoxigenin nick-end labeling (TUNEL), and then tartrate-resistant acid phosphatase (TRAP) activity was determined on the same sections. Epon-embedded specimens were sectioned serially into 0.5-mum semithin sections; some of these sections were re-embedded in Epon, sectioned into 0.1-mum ultrathin sections, and observed by TEM. IHC revealed that the nuclei of TRAP-positive odontoclasts on the dentine were generally TUNEL-negative. Around these odontoclasts, a few TRAP-positive structures were present together with TUNEL-positive structures, e.g., a TRAP-positive structure with one TUNEL-positive nucleus, a TRAP-positive structure with one TUNEL-positive nucleus plus one or two TUNEL-negative nuclei, or a TRAP-positive structure with no nucleus. By TEM, some odontoclasts showed nuclear fragments including compacted chromatin. The results suggest that, during apoptosis, odontoclasts fragment into variously sized cellular parts including three or fewer nuclei.
机译:这项研究旨在确定人乳牙的生理性根吸收过程中成牙本质细胞的凋亡。将乳牙固定,脱钙并嵌入石蜡中以进行免疫组织化学(IHC)观察,并嵌入Epon中以进行透射电子显微镜(TEM)。通过末端脱氧核苷酸转移酶(TdT)介导的dUTP-洋地黄毒苷缺口末端标记(TUNEL)鉴定凋亡细胞,然后在相同的切片上测定抗酒石酸酸性磷酸酶(TRAP)活性。将嵌入Epon的标本依次切成0.5微米的半薄切片。其中一些切片被重新嵌入Epon,切片成0.1微米的超薄切片,并用TEM观察。 IHC显示,牙本质上TRAP阳性齿质破骨细胞的核通常为TUNEL阴性。在这些齿质破骨细胞周围,存在一些TRAP阳性结构以及TUNEL阳性结构,例如具有一个TUNEL阳性核的TRAP阳性结构,具有一个TUNEL阳性核加一个或两个TUNEL-的TRAP阳性结构。阴性核或没有核的TRAP阳性结构。通过TEM,一些齿破骨细胞显示出核碎片,包括紧密的染色质。结果表明,在凋亡过程中,齿破骨细胞分裂成各种大小的细胞部分,包括三个或更少的核。

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