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移植成年T细胞白血病细胞的SCID小鼠中甲状旁腺激素相关蛋白诱导的高钙血症

Parathyroid hormone-related protein-induced hypercalcemia in SCID mice engrafted with adult T-cell leukemia cells.

作者信息

Takaori-Kondo A, Imada K, Yamamoto I, Kunitomi A, Numata Y, Sawada H, Uchiyama T

机构信息

Institute for Virus Research, Kyoto University, Sakyo-ku, Kyoto, Japan.

出版信息

Blood. 1998 Jun 15;91(12):4747-51.

PMID:9616173
Abstract

Parathyroid hormone-related protein (PTHrP) is considered to be one of the main causes of hypercalcemia associated with adult T-cell leukemia (ATL). To clarify the role of PTHrP and bone remodeling in the development of hypercalcemia in ATL, we examined the SCID mouse model of ATL that has previously been shown to mimic the disease in humans. Using this model, we found clear elevations in serum levels of calcium and C-terminal PTHrP (C-PTHrP). PTHrP mRNA was highly expressed in ATL cells proliferating in vivo. After the development of hypercalcemia, ATL mice were killed and bone histomorphometric analysis was performed. Bone volume was clearly decreased in the ATL mice. In comparison to control SCID mice, bone formation indices were very low in the ATL mice. Surprisingly, no significant difference was detected between the ATL mice and the control SCID mice in eroded surface/bone surface (ES/BS), a parameter of bone resorption. To our knowledge, the model presented here is the first animal model of ATL with humoral hypercalcemia. This is in contrast to previously reported, well-characterized animal models of human solid tumors associated with humoral hypercalcemia of malignancy (HHM). Furthermore, this model not only provides us with the opportunity to study the mechanisms underlying development of elevated calcium levels in ATL, but also allows us to test new therapeutic agents designed to treat hypercalcemia.

摘要

甲状旁腺激素相关蛋白(PTHrP)被认为是与成人T细胞白血病(ATL)相关的高钙血症的主要原因之一。为了阐明PTHrP和骨重塑在ATL高钙血症发生发展中的作用,我们研究了先前已被证明可模拟人类疾病的ATL SCID小鼠模型。利用该模型,我们发现血清钙和C末端PTHrP(C-PTHrP)水平明显升高。PTHrP mRNA在体内增殖的ATL细胞中高表达。高钙血症发生后,处死ATL小鼠并进行骨组织形态计量学分析。ATL小鼠的骨体积明显减少。与对照SCID小鼠相比,ATL小鼠的骨形成指数非常低。令人惊讶的是,在骨吸收参数侵蚀表面/骨表面(ES/BS)方面,ATL小鼠与对照SCID小鼠之间未检测到显著差异。据我们所知,这里提出的模型是第一个伴有体液性高钙血症的ATL动物模型。这与先前报道的、特征明确的与恶性肿瘤体液性高钙血症(HHM)相关的人类实体瘤动物模型形成对比。此外,该模型不仅为我们提供了研究ATL中钙水平升高的潜在机制的机会,还使我们能够测试旨在治疗高钙血症的新型治疗药物。

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