Yano S, Sugimoto T, Tsukamoto T, Chihara K, Kobayashi A, Kitazawa S, Maeda S, Kitazawa R
Third Division, Department of Medicine, Kobe University School of Medicine, Kobe, Japan.
Kidney Int. 2000 Nov;58(5):1980-6. doi: 10.1111/j.1523-1755.2000.00370.x.
The down-regulation of both calcium-sensing receptor (CaSR) and vitamin D receptor (VDR) in parathyroid (PT) glands of secondary hyperparathyroidism (HPT) caused by chronic renal failure has been associated with PT hormone hypersecretion as well as PT hypergrowth. To clarify the predominance of decreased expression of CaSR and VDR in the high proliferative activity of PT glands, we examined the relationship between the expression of both receptors and proliferative activity in human PT glands.
Serial sections of 56 PT glands, including 52 glands from secondary HPT and 4 normal PT glands resected together with thyroid carcinoma, were examined immunohistochemically with specific antibodies against CaSR, VDR, and Ki67. The Ki67-positive cell number was counted and expressed as the Ki67 score. The CaSR and VDR expressions were semiquantitatively analyzed.
The expressions of both CaSR and VDR were markedly decreased in PT glands of secondary HPT, while the Ki67 score was significantly higher than it was in normal controls. When hyperplastic glands were classified into two subgroups, with [N(+)] or without [N(-)] nodular formation, CaSR expression was significantly decreased in N(+), while VDR expression was not different. Multiple regression analyses revealed that the decreased expression of CaSR could contribute significantly to the high proliferative activity, even if VDR expression was taken into account.
The decrease in CaSR expression is associated with the high proliferative activity of PT glands in secondary HPT, independently of the decreased VDR expression. These findings provide a new insight into the pathogenesis of PT hyperplasia, which is refractory to vitamin D therapy in patients with severe secondary HPT.
慢性肾衰竭所致继发性甲状旁腺功能亢进(HPT)患者甲状旁腺(PT)中钙敏感受体(CaSR)和维生素D受体(VDR)的下调与PT激素分泌过多以及PT过度生长有关。为阐明CaSR和VDR表达降低在PT腺体高增殖活性中的主导作用,我们研究了人PT腺体中这两种受体的表达与增殖活性之间的关系。
对56个PT腺体的连续切片进行免疫组织化学检查,其中包括52个来自继发性HPT的腺体以及4个与甲状腺癌一起切除的正常PT腺体,使用针对CaSR、VDR和Ki67的特异性抗体。计数Ki67阳性细胞数并表示为Ki67评分。对CaSR和VDR的表达进行半定量分析。
继发性HPT患者的PT腺体中CaSR和VDR的表达均明显降低,而Ki67评分显著高于正常对照组。当增生性腺体分为有[N(+)]或无[N(-)]结节形成的两个亚组时,N(+)组中CaSR表达明显降低,而VDR表达无差异。多元回归分析显示,即使考虑VDR表达,CaSR表达降低也可能对高增殖活性有显著影响。
CaSR表达降低与继发性HPT中PT腺体的高增殖活性相关,独立于VDR表达降低。这些发现为PT增生的发病机制提供了新的见解,PT增生在严重继发性HPT患者中对维生素D治疗无效。