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[维生素D对人体作用的分子研究方法]

[Molecular approach to the action of vitamin D in man].

作者信息

Thomasset M, Perret C, Brehier A, Balmain N, Cuisinier-Gleizes P, Mathieu H

出版信息

Arch Fr Pediatr. 1985 Mar;42(3):231-6.

PMID:2988477
Abstract

Some applications to man of specific markers of the molecular action of vitamin D (1.25(OH)2D3 receptors and antibodies to hormone-dependent proteins (CaBP and cDNA] are reported in this study. On case of type II vitamin-dependent rickets was characterized by 1.25(OH)2D3 plasma level greater than 250 pg/ml and a ten-fold decrease of the number of binding sites of the hormone in cultured skin fibroblasts. We propose that CaBP 28K and/or 9K-containing cells, such as Purkinje's cells and chondroblasts may be targets for vitamin D action. Detection in fetuses, from the 20th week of gestation, of CaBP 9K messenger RNA in the duodenum and sternum and presence of CaBP 28K and 9K in the chondroblasts of the upper extremity of tibia, suggest that vitamin D acts on the nucleus of its target-cells during fetal development. Finally, discovery of the gene of CaBP 9K in man opens the prospect of studies which will improve the understanding of the mechanism of action of vitamin D.

摘要

本研究报道了维生素D分子作用的特定标志物(1,25-二羟维生素D3受体以及激素依赖性蛋白(钙结合蛋白和互补DNA)的抗体)在人体中的一些应用。在II型维生素依赖性佝偻病病例中,其特征为血浆1,25-二羟维生素D3水平高于250皮克/毫升,且培养的皮肤成纤维细胞中激素结合位点数量减少了十倍。我们提出,含28K和/或9K钙结合蛋白的细胞,如浦肯野细胞和成软骨细胞,可能是维生素D作用的靶点。在妊娠20周起的胎儿十二指肠和胸骨中检测到9K钙结合蛋白信使核糖核酸,以及在胫骨上端成软骨细胞中存在28K和9K钙结合蛋白,这表明维生素D在胎儿发育过程中作用于其靶细胞的细胞核。最后,人类9K钙结合蛋白基因的发现为深入了解维生素D作用机制的研究开辟了前景。

相似文献

1
[Molecular approach to the action of vitamin D in man].[维生素D对人体作用的分子研究方法]
Arch Fr Pediatr. 1985 Mar;42(3):231-6.
2
Vitamin D-dependent calcium-binding proteins (CaBPs) in human fetuses: comparative distribution of 9K CaBP mRNA and 28K CaBP during development.人类胎儿中的维生素D依赖性钙结合蛋白(CaBPs):发育过程中9K CaBP mRNA和28K CaBP的比较分布
Pediatr Res. 1987 Apr;21(4):362-7. doi: 10.1203/00006450-198704000-00008.
3
The vitamin D hormone and its nuclear receptor: molecular actions and disease states.维生素D激素及其核受体:分子作用与疾病状态。
J Endocrinol. 1997 Sep;154 Suppl:S57-73.
4
Selective biological response by target organs (intestine, kidney, and bone) to 1,25-dihydroxyvitamin D3 and two analogues.靶器官(肠道、肾脏和骨骼)对1,25 - 二羟维生素D3及其两种类似物的选择性生物学反应。
Cancer Res. 1993 Sep 1;53(17):3935-42.
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Effect of dietary calcium and 1,25-(OH)2D3 on the expression of calcium transport genes in calbindin-D9k and -D28k double knockout mice.膳食钙和1,25-(OH)₂D₃对钙结合蛋白-D9k和-D28k双敲除小鼠钙转运基因表达的影响
Biochem Biophys Res Commun. 2009 Feb 6;379(2):227-32. doi: 10.1016/j.bbrc.2008.12.029. Epub 2008 Dec 25.
6
1,25(OH)2D3-dependent regulation of calbindin-D28k mRNA requires ongoing protein synthesis in chick duodenal organ culture.1,25-二羟维生素D3对钙结合蛋白-D28k mRNA的依赖性调节需要雏鸡十二指肠器官培养中持续的蛋白质合成。
J Cell Biochem. 1995 Jul;58(3):315-27. doi: 10.1002/jcb.240580306.
7
Effects of calcitonin and parathyroid hormone on the regulation of cabindin-D(9k) in the uterus, placenta, and fetal membrane of rats related to blood calcium level during late gestation.降钙素和甲状旁腺激素对妊娠晚期大鼠子宫、胎盘和胎膜中与血钙水平相关的钙结合蛋白-D(9k)调节的影响。
Mol Reprod Dev. 2007 Sep;74(9):1188-97. doi: 10.1002/mrd.20627.
8
Complex regulation of Calbindin-D(9k) in the mouse placenta and extra-embryonic membrane during mid- and late pregnancy.妊娠中期和晚期小鼠胎盘及胚外膜中钙结合蛋白-D(9k)的复杂调控
Mol Cell Endocrinol. 2004 Feb 12;214(1-2):39-52. doi: 10.1016/j.mce.2003.11.029.
9
Defective binding and function of 1,25-dihydroxyvitamin D3 receptors in peripheral mononuclear cells of patients with end-organ resistance to 1,25-dihydroxyvitamin D.1,25-二羟维生素D3受体在对1,25-二羟维生素D终末器官抵抗患者外周血单个核细胞中的结合及功能缺陷
J Clin Invest. 1985 Nov;76(5):2012-5. doi: 10.1172/JCI112201.
10
Capacity of 1,25-dihydroxyvitamin D to stimulate expression of calbindin D changes with age in the rat.1,25 - 二羟维生素D刺激钙结合蛋白D表达的能力在大鼠中随年龄而变化。
Arch Biochem Biophys. 1998 Apr 15;352(2):159-64. doi: 10.1006/abbi.1998.0594.

引用本文的文献

1
Analysis and in situ detection of cholecalcin messenger RNA (9000 Mr CaBP) in the uterus of the pregnant rat.妊娠大鼠子宫中胆钙蛋白信使核糖核酸(9000Mr CaBP)的分析及原位检测
Cell Tissue Res. 1987 Jan;247(1):51-7. doi: 10.1007/BF00216546.