Sela-Brown A, Russell J, Koszewski N J, Michalak M, Naveh-Many T, Silver J
Minerva Center for Calcium and Bone Metabolism, Hadassah University Hospital and Hebrew University Medical School, Jerusalem, Israel.
Mol Endocrinol. 1998 Aug;12(8):1193-200. doi: 10.1210/mend.12.8.0148.
1,25-dihydroxyvitaminD3 [1,25-(OH)2D3] and PTH both act to increase serum calcium. In addition, 1,25-(OH)2D3 decreases PTH gene transcription, which is relevant both to the physiology of calcium homeostasis and to the management of the secondary hyperparathyroidism of patients with chronic renal failure. In chronic hypocalcemia there is secondary hyperparathyroidism with increased levels of PTH mRNA and serum PTH despite markedly increased levels of 1,25-(OH)2D3. We have studied the role of calreticulin in this resistance to 1,25-(OH)2D3. Weanling rats fed a low-calcium diet were hypocalcemic and had increased PTH mRNA levels despite high serum 1,25-(OH)2D3 levels. 1,25-(OH)2D3 given by continuous minipump infusion to normal rats led to the expected decrease in PTH mRNA. The hypocalcemic rats had an increased concentration of calreticulin in the nuclear fraction of their parathyroids, but not in other tissues. Gel shift assays showed that a purified vitamin D receptor and retinoid X receptor-beta bound to the PTH promoter's chicken and rat vitamin D response element (VDRE), and this binding was inhibited by added pure calreticulin. Transfection studies with a PTH VDRE-chloramphenicol acetyltransferase (CAT) construct showed that 1,25-(OH)2D3 decreased CAT transcription. Cotransfection of PTH VDRE-CAT with a calreticulin expression vector in the sense orientation prevented the transcriptional effect of 1,25-(OH)2D3, but a calreticulin vector in the antisense orientation had no effect. These results show that calreticulin prevents the binding of vitamin D receptor-retinoid X receptor-beta to the PTH VDRE in gel retardation assays and prevents the transcriptional effect of 1,25-(OH)2D3 on the PTH gene. This is the first report of calreticulin inhibiting a down-regulatory function of a sterol hormone and may help explain the refractoriness of the secondary hyperparathyroidism of many chronic renal failure patients to 1,25-(OH)2D3.
1,25 - 二羟维生素D3 [1,25 - (OH)2D3] 和甲状旁腺激素(PTH)都能提高血清钙水平。此外,1,25 - (OH)2D3可降低PTH基因转录,这与钙稳态生理以及慢性肾衰竭患者继发性甲状旁腺功能亢进的治疗均相关。在慢性低钙血症中,尽管1,25 - (OH)2D3水平显著升高,但仍存在继发性甲状旁腺功能亢进,PTH mRNA和血清PTH水平升高。我们研究了钙网蛋白在这种对1,25 - (OH)2D3抵抗中的作用。喂食低钙饮食的断乳大鼠出现低钙血症,尽管血清1,25 - (OH)2D3水平较高,但PTH mRNA水平升高。通过连续微量泵输注给予正常大鼠1,25 - (OH)2D3导致PTH mRNA如预期般下降。低钙血症大鼠甲状旁腺细胞核部分的钙网蛋白浓度升高,但其他组织中未升高。凝胶迁移试验表明,纯化的维生素D受体和视黄酸X受体 - β与PTH启动子的鸡和大鼠维生素D反应元件(VDRE)结合,而添加的纯钙网蛋白可抑制这种结合。用PTH VDRE - 氯霉素乙酰转移酶(CAT)构建体进行的转染研究表明,1,25 - (OH)2D3可降低CAT转录。将PTH VDRE - CAT与有义方向的钙网蛋白表达载体共转染可阻止1,25 - (OH)2D3的转录作用,但反义方向的钙网蛋白载体则无此作用。这些结果表明,在凝胶阻滞试验中钙网蛋白可阻止维生素D受体 - 视黄酸X受体 - β与PTH VDRE结合,并阻止1,25 - (OH)2D3对PTH基因的转录作用。这是关于钙网蛋白抑制甾体激素下调功能的首次报道,可能有助于解释许多慢性肾衰竭患者继发性甲状旁腺功能亢进对1,25 - (OH)2D3难治的原因。