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大鼠切牙中维生素D受体和钙结合蛋白基因的细胞及阶段特异性表达:1,25 - 二羟基维生素D3的调节作用

Cell- and stage-specific expression of vitamin D receptor and calbindin genes in rat incisor: regulation by 1,25-dihydroxyvitamin D3.

作者信息

Berdal A, Hotton D, Pike J W, Mathieu H, Dupret J M

机构信息

INSERM U 120, Hôpital Robert Debré, Paris, France.

出版信息

Dev Biol. 1993 Jan;155(1):172-9. doi: 10.1006/dbio.1993.1016.

Abstract

To investigate the extent of 1,25-dihydroxyvitamin D3 [1,25(OH)2D3] action and its relationships to calbindin gene expression in mineralized tissues, we have analyzed rat incisors with different probes, including a vitamin D receptor (VDR) antibody and specific cDNAs to rat calbindin-D9K and calbindin-D28K. Developmental and hormonal controls of calbindin gene expression were investigated by Northern blot analysis of ameloblast and odontoblast mRNA. Distribution and hormone-induced changes of VDR were also studied by light microscopic immunocytochemistry. A differential tissue- and stage-specific expression of the calbindin genes was observed in microdissected portions of the continuously erupting incisor. The two calbindins were expressed in ameloblasts, whereas only calbindin-D28K was expressed in odontoblasts. Moreover, in ameloblasts, expression of calbindin-D28K preceded that of calbindin-D9K. Immunoreactivity for VDR was present in all progenitor cells and progressively decreased during the differentiation process, whereas, in differentiated tissues, a hormonal upregulation was restricted to hard tissue-forming cells, i.e., ameloblasts and odontoblasts. Furthermore, calbindin gene expression appeared to be regulated by 1,25(OH)2D3. Taken together, these data indicate that ameloblasts and odontoblasts are target cells for 1,25(OH)2D3 and provide the first insights into the hormonal control of tooth genes during development.

摘要

为了研究1,25 - 二羟基维生素D3 [1,25(OH)2D3] 的作用程度及其与矿化组织中钙结合蛋白基因表达的关系,我们用不同的探针分析了大鼠切牙,包括维生素D受体 (VDR) 抗体以及大鼠钙结合蛋白-D9K和钙结合蛋白-D28K的特异性cDNA。通过对成釉细胞和成牙本质细胞mRNA的Northern印迹分析,研究了钙结合蛋白基因表达的发育和激素调控。还通过光学显微镜免疫细胞化学研究了VDR的分布和激素诱导的变化。在连续萌出的切牙的显微切割部分观察到钙结合蛋白基因的组织和阶段特异性差异表达。两种钙结合蛋白在成釉细胞中表达,而成牙本质细胞中仅表达钙结合蛋白-D28K。此外,在成釉细胞中,钙结合蛋白-D28K的表达先于钙结合蛋白-D9K。VDR的免疫反应性存在于所有祖细胞中,并在分化过程中逐渐降低,而在分化组织中,激素上调仅限于形成硬组织的细胞,即成釉细胞和成牙本质细胞。此外,钙结合蛋白基因表达似乎受1,25(OH)2D3调控。综上所述,这些数据表明成釉细胞和成牙本质细胞是1,25(OH)2D3的靶细胞,并为发育过程中牙齿基因的激素调控提供了初步见解。

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