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Localization of Metallothionein (MT) and Expression of MT Isoforms Induced by Cadmium in Rat Dental Pulp

机译:镉诱导大鼠牙髓中金属硫蛋白的定位和MT亚型的表达

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References(39) Cited-By(3) We investigated the induction of metallothionein (MT) by cadmium (Cd) in the dental pulp of rat incisors. Time-course studies of MT mRNA expression after single Cd injection were observed by Northern-blot analysis. The isoform-specific expressions of MT mRNAs (MT-I, MT-II and MT-III) were observed using the reverse transcriptase-polymerase chain reaction (RT-PCR) method. Both MT-I and MT-II mRNA levels increased within 3 h, peaked at 3 h and then decreased. These findings demonstrated that MT-I and MT-II mRNA were rapidly induced by Cd in dental pulp. MT-III mRNA was constitutively expressed in rat dental pulp, but the expression level did not change by Cd treatment. The localization of MT protein in Cd-treated rat dental pulp was determined by immunohistochemical staining using anti-MT antibody against MT-I and MT-II. MT protein was localized in the specific cell type of odontoblasts (secretory odontoblasts and resting odontoblasts). In conclusion, it is likely that stained MT in the immunohistochemical study should be MT-I and/or MT-II. Furthermore, MT-I and/or MT-II in Cd-treated rat dental pulp was localized in odontoblasts, in which accumulation of Cd were reported. The cell-specific synthesis of MT may be associated with its metal storage and detoxification role in dental tissues.
机译:参考文献(39)被引用者(3)我们研究了在大鼠门牙牙髓中镉(Cd)对金属硫蛋白(MT)的诱导作用。通过Northern印迹分析观察了单次镉注射后MT mRNA表达的时程研究。使用逆转录-聚合酶链反应(RT-PCR)方法观察到MT mRNA的同工型特异性表达(MT-1,MT-II和MT-III)。 MT-I和MT-II mRNA水平均在3小时内升高,在3小时达到峰值,然后下降。这些发现表明,牙髓中的镉可快速诱导MT-I和MT-II mRNA。 MT-III mRNA在大鼠牙髓中组成性表达,但Cd处理后表达水平未改变。使用抗MT-I和MT-II的抗MT抗体,通过免疫组织化学染色确定了Cd处理的大鼠牙髓中MT蛋白的定位。 MT蛋白位于成牙本质细胞(分泌性成牙本质细胞和静息成牙本质细胞)的特定细胞类型中。总之,免疫组织化学研究中染色的MT可能应该是MT-I和/或MT-II。此外,Cd处理过的大鼠牙髓中的MT-I和/或MT-II位于成牙本质细胞中,据报道其中有Cd积累。 MT的细胞特异性合成可能与其在牙齿组织中的金属存储和解毒作用有关。

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