首页> 外文期刊>Journal of Endocrinological Investigation: Official Journal of the Italian Society of Endocrinology >Absence of response to human parathyroid hormone in athymic mice grafted with human parathyroid adenoma, hyperplasia or parathyroid cells maintained in culture.
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Absence of response to human parathyroid hormone in athymic mice grafted with human parathyroid adenoma, hyperplasia or parathyroid cells maintained in culture.

机译:在培养的人甲状旁腺腺瘤,增生或甲状旁腺细胞移植的胸腺小鼠中,对人甲状旁腺激素无反应。

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摘要

In athymic mice we have developed a model of long-term human PTH hypersecretion, using xenotransplantation of respectively parathyroid gland fragments obtained from patients with primary (primary) or secondary (secondary) uremic hyperparathyroidism (HPT), and parathyroid cells maintained in culture from patients with secondary uremic HPT. Both grafted parathyroid tissue fragments and cultured cells induced prolonged and marked secretion of human intact PTH (iPTH) in nude mice. Despite extremely high plasma iPTH levels, hypercalcemia or hypophosphatemia was not observed. Moreover, PTH secretion was not significantly modified by low-calcium, high-phosphate diet for 3 weeks. Four mice which had a mean plasma human iPTH level of 237+/-152 pg/ml for more than 9 months and 4 age-matched, sham-grafted control mice with undetectable human iPTH levels underwent bone histomorphometry examination. No difference was found between the two groups with respect to active bone resorption surface or number of osteoclasts/mm2. We hypothesize that the characteristic deficit of T cell function and of cytokine and growth factor production may protect nude mice with chronic hypersecretion of human PTH from hypercalcemia and bone lesions. We suggest that this strain of mice could be used for better understanding the relationship between cytokines and bone turnover.
机译:在无胸腺小鼠中,我们使用异种移植分别从患有原发性(原发性)或继发性(继发性)尿毒症甲状旁腺功能亢进症(HPT)的患者的甲状旁腺腺体以及患者体内培养的甲状旁腺细胞,建立了长期人类PTH过度分泌的模型继发性尿毒症HPT。移植的甲状旁腺组织碎片和培养的细胞均可诱导裸鼠中人完整PTH(iPTH)的延长和明显分泌。尽管血浆iPTH水平极高,但未观察到高钙血症或低磷血症。此外,低钙,高磷酸盐饮食持续3周对PTH的分泌没有显着影响。对四只平均血浆人iPTH水平为237 +/- 152 pg / ml的小鼠进行了9个月以上的测试,并对四只年龄相匹配的假iPTH水平未检测到的对照小鼠进行了骨组织形态学检查。两组之间在活性骨吸收表面或破骨细胞数量/ mm2之间没有差异。我们假设,T细胞功能以及细胞因子和生长因子产生的特征缺陷可能保护具有慢性PTH分泌过多的裸鼠免于高钙血症和骨损伤。我们建议这种小鼠品系可用于更好地了解细胞因子与骨转换之间的关系。

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