Ishizuka Yoichi, Yoshida Mizuki, Ambe Kimiharu, Sasaki Junzo, Sugihara Naoki, Watanabe Hiroki
Department of Epidemiology and Public Health, Tokyo Dental College.
Gunma Oral Health Center for Special Needs Dentistry.
Bull Tokyo Dent Coll. 2019 Dec 10;60(4):261-266. doi: 10.2209/tdcpublication.2019-0003. Epub 2019 Nov 23.
Active oxygen and free radicals are involved in metabolism in cells and tissues. Immunohistological studies of related enzymes are few, and the morphological dynamics of these enzymes in dental pulp and odontoblasts remain to be elucidated. Nitric oxide synthase (NOS) has 3 isoforms: nNOS, iNOS, and eNOS. The aim of this study was to investigate the profiles of NOS isoforms in the absence of nNOS in dental pulp and odontoblasts. Five-week-old male C57BL/6 and nNOS knockout (KO) mice were sacrificed and expression of nNOS, iNOS, and eNOS determined immunohistochemically. Expression of nNOS was positive, whereas that of iNOS was negative and eNOS weakly positive in the dental pulp and odontoblasts of the control mice. In nNOS KO mice, expression of iNOS was positive in dental pulp and strongly positive in odontoblasts, whereas that of eNOS was stronger in fibroblasts, endothelial cells in the vicinity of blood vessels in the dental pulp, and odontoblasts. Expression of nNOS was negative in the nNOS KO mice. This suggests that iNOS and eNOS compensate for nNOS deficiency in vascular endothelial cells and fibroblasts in the dental pulp and odontoblasts.
活性氧和自由基参与细胞和组织的代谢。相关酶的免疫组织学研究较少,这些酶在牙髓和成牙本质细胞中的形态动力学仍有待阐明。一氧化氮合酶(NOS)有3种同工型:神经元型一氧化氮合酶(nNOS)、诱导型一氧化氮合酶(iNOS)和内皮型一氧化氮合酶(eNOS)。本研究的目的是调查在牙髓和成牙本质细胞中缺乏nNOS时NOS同工型的情况。处死5周龄雄性C57BL/6和nNOS基因敲除(KO)小鼠,通过免疫组织化学法测定nNOS、iNOS和eNOS的表达。在对照小鼠的牙髓和成牙本质细胞中,nNOS表达呈阳性,而iNOS表达呈阴性,eNOS表达呈弱阳性。在nNOS KO小鼠中,iNOS在牙髓中表达呈阳性,在成牙本质细胞中表达呈强阳性,而eNOS在成纤维细胞、牙髓血管附近的内皮细胞和成牙本质细胞中表达更强。nNOS KO小鼠中nNOS表达呈阴性。这表明iNOS和eNOS可补偿牙髓和成牙本质细胞中血管内皮细胞和成纤维细胞的nNOS缺陷。