Division of Medical Cell Biology, Institute for Anatomy and Cell Biology II, Justus Liebig University, Aulweg 123, 35385, Giessen, Germany.
Histochem Cell Biol. 2013 Oct;140(4):443-62. doi: 10.1007/s00418-013-1131-8. Epub 2013 Aug 28.
Patients with mild forms of peroxisomal biogenesis disorders show facial dysmorphism and exhibit dentition problems accompanied by enamel hypoplasia. However, no information is available on the role of peroxisomes in dental and paradontal tissues. Therefore, we studied the distribution of these organelles, their protein composition and the expression of corresponding genes during dental development and in mature decalcified teeth in mice. Perfusion-fixed heads of mice of different developmental stages (E13.5 to adult) were cut in sagittal direction into two halves and embedded in paraffin for serial sectioning and subsequent peroxidase-based immunohistochemistry or double-immunofluorescence preparations. Frozen, unfixed heads of newborn mice were used for cryosectioning and subsequent laser-assisted microdissection of ameloblasts and odontoblasts, RNA isolation and RT-PCR analysis. Our results revealed the presence of peroxisomes already in the bud stage of dental development. An increase in peroxisome abundance was noted during differentiation of ameloblasts and odontoblasts with the highest number of organelles in Tomes' processes of mature ameloblasts. A strong heterogeneity of peroxisomal enzyme content developed within differentiated dental cell types. A drastic down-regulation of catalase in maturing ameloblasts was noted in contrast to high levels of lipid metabolizing enzymes in peroxisomes of these cells. As known from the literature, differentiated ameloblasts are more prone to oxidative damage which could be explained by the low catalase levels inside of this cell type.
患有过氧化物酶体生物发生障碍轻度形式的患者表现出面部畸形,并表现出牙列问题伴有釉质发育不全。然而,关于过氧化物酶体在牙齿和牙周组织中的作用尚无信息。因此,我们研究了这些细胞器在小鼠牙齿发育过程中和成熟脱矿牙中的分布、它们的蛋白质组成以及相应基因的表达。将来自不同发育阶段(E13.5 至成年)的小鼠的灌注固定头部沿矢状方向切成两半,并嵌入石蜡中进行连续切片,随后进行过氧化物酶免疫组织化学或双重免疫荧光制备。使用新生小鼠的冷冻、未固定的头部进行冷冻切片,随后进行成釉细胞和成牙本质细胞的激光辅助显微切割、RNA 分离和 RT-PCR 分析。我们的结果表明,过氧化物酶体已经存在于牙齿发育的萌芽阶段。在成釉细胞和成牙本质细胞的分化过程中,过氧化物酶体的数量增加,在成熟成釉细胞的 Tomes 突中数量最多。在分化的牙齿细胞类型中,过氧化物酶的酶含量表现出强烈的异质性。与这些细胞中过氧化物酶内高水平的脂质代谢酶相反,成熟成釉细胞中的过氧化氢酶水平明显下调。如文献所述,分化的成釉细胞更容易受到氧化损伤,这可以通过该细胞类型内低水平的过氧化氢酶来解释。